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Tropical Viruses • Arbovirals • Emerging Infectious Disease

Tropical & Infectious Disease ELISA

From Dengue NS1 and IgG/IgM serology across all four serotypes to Zika envelope protein, Chikungunya, Yellow Fever, Japanese Encephalitis, Rabies glycoprotein, Hepatitis B/C, RSV, Influenza, CRM197 vaccine manufacturing QC, and dsRNA innate immunity ELISA — Krishgen's infectious disease platform covers the pathogens that matter most to researchers in Asia, Africa, and Latin America in 2026.

15+
Tropical Virus Targets
5
Rabies Assays — Ag & Ab
4
Dengue Assay Types
50+
SARS-CoV-2 Assays
2026 Research Context Why Tropical Infectious Disease ELISA Are a Priority in 2026
Expanding Arboviral GeographyClimate-driven range expansion of Aedes aegypti and Aedes albopictus mosquitoes is pushing dengue, Zika, chikungunya, and yellow fever into new regions. Dengue alone recorded over 7 million cases globally in 2024 — the highest annual burden ever documented — making immunogenicity and seroprevalence ELISA a critical research infrastructure tool.
Vaccine Development PipelineNew vaccine candidates for dengue (tetravalent subunit), chikungunya (VLP and mRNA), Zika, and rabies (next-generation intradermal) are all in active clinical trials in 2026. Each requires validated IgG/IgM titration ELISA, antigen characterisation assays, and neutralisation surrogates to measure immunogenicity endpoints in pre-clinical models and human trial cohorts.
Serosurveillance & One HealthPost-pandemic infectious disease monitoring has elevated investment in serosurveillance infrastructure across South Asia, Southeast Asia, and sub-Saharan Africa. Krishgen's ISO 13485-manufactured ELISA — with WHO TRS-referenced validation — provide the lot-to-lot consistency and documentation required for multi-site seroprevalence studies and cross-laboratory harmonisation.
Portfolio Overview

Four Integrated Infectious Disease Research Areas

Krishgen's infectious disease ELISA portfolio is built around the pathogens driving the greatest research investment globally in 2026. The range spans arboviral serology, vaccine manufacturing QC, respiratory and hepatic viruses, and archived SARS-CoV-2 research assays — all KRIBIOLISA™ or GENLISA™ branded, ISO 13485-manufactured in Mumbai and California.

``` ◉ ARBOVIRALS — PRIMARY FOCUS
Dengue • Zika • Chikungunya • Yellow Fever • JEV
Mosquito-borne flaviviruses & alphaviruses • IgG / IgM / Antigen / NS1
Dengue IgG / IgM / NS1 DENV 1–4 Serotype Coverage Zika NS1 • KBVH650 (50 pg/ml) Zika Envelope • KBVH700 (180 pg/ml) Chikungunya IgG / IgM Yellow Fever IgG • KBVH605 Japanese Encephalitis (JEV)
Explore arboviral ELISA →
◉ RABIES — 5-ASSAY PANEL
Rabies Glycoprotein, Nucleoprotein & IgG Antibody ELISA
Antigen + Antibody panel • Glycoprotein & Nucleoprotein targets • IgG subtypes 1, 2, 3
★ KBVH177 — Glycoprotein Antigen (0–10 IU/ml) ★ KBVH180 — Nucleoprotein Antigen (0–10 IU/ml) KBVH077 — IgG (subtypes 1,2,3) KBVH277 — IgG Nucleoprotein KBVH377 — IgG Glycoprotein 6.25–200 U/ml Antibody Range
Explore rabies ELISA panel →
◉ HEPATITIS • RSV • INFLUENZA • VZV
Respiratory, Hepatic & Systemic Viral ELISA
Hepatitis B & C • Influenza A/B • RSV • VZV • HIV • Mumps • Measles
HBsAg / HBsAb / HBeAg / HBcAg HCV Antibody ELISA Influenza A/B (H1N1, H3N2) RSV Antigen ELISA VZV IgG • KBVH601 (8 ng/ml) VZV IgM • KBVH602
Explore respiratory & hepatitis ELISA →
◉ SARS-COV-2 RESEARCH
SARS-CoV-2 Antigen, Antibody & sVNT ELISA
50+ assays • 5 species • 6 variant sVNT • Pre-clinical to clinical
Spike S1 / S2 / RBD / Whole Spike Nucleocapsid / Envelope / Membrane IgG / IgM Quantitative Titration sVNT — 6 Variants (BSL-2) Mouse • Rat • Hamster • Rabbit • Human
Explore SARS-CoV-2 assays →
◉ VACCINE MANUFACTURING QC
CRM197 Carrier Protein Quantification ELISA
Conjugate vaccine in-process & release testing • WHO TRS • ICH Q2(R2)/Q14
★ KBVH500 — CRM197 (5 µg/ml LOD) Pneumococcal / Meningococcal / Hib / Typhoid Validated vs Fina Biosolutions EcoCRM™ Polysaccharide-conjugate matrix ICH Q2(R2)/Q14 • WHO TRS-aligned
Explore CRM197 ELISA →
◉ INNATE ANTIVIRAL IMMUNITY
dsRNA Detection ELISA — Viral Replication & mRNA Vaccine QC
Double-stranded RNA • J2 antibody • RNA virus replication marker • mRNA vaccine manufacturing
★ KBBA56 — dsRNA J2 ELISA Dengue • Zika • CHIKV • Influenza • SARS-CoV-2 replication TLR3 / MDA5 / RIG-I Pathway Research mRNA Vaccine dsRNA Contaminant QC IFN-β / Innate Immune Sensing
Explore dsRNA ELISA →
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Browse by Pathogen

Infectious Disease Assay Targets

Filter by pathogen class to find the right ELISA. All kits are sandwich ELISA, HRP/TMB colorimetric, 96-well break-apart, ISO 13485-manufactured. Validated against Krishgen's seven-point "Gold Ring" QC protocol.

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Dengue Virus
Arboviral

Dengue affects 400 million people annually across 100+ countries. ELISA-based serology distinguishes primary from secondary infection, measures vaccine-induced IgG seroconversion, and detects NS1 antigen during the pre-antibody viraemic window. All four DENV serotypes are covered.

Dengue IgG (DENV 1–4)Dengue IgM ELISANS1 Antigen ELISASerum / Plasma
View Dengue ELISA →
Zika Virus
Arboviral

Zika (ZIKV) causes congenital microcephaly in neonates of infected mothers. Krishgen offers two orthogonal antigen assays — NS1 protein (KBVH650, 50 pg/ml) for acute detection and envelope protein (KBVH700, 180 pg/ml) for vaccine antigen characterisation — plus IgG/IgM serology.

KBVH650 NS1 (50 pg/ml)KBVH700 Envelope (180 pg/ml)IgG / IgM SerologyStrain SPH2015
View Zika NS1 ELISA →
Chikungunya Virus
Arboviral

CHIKV is a re-emerging alphavirus causing debilitating polyarthralgia, now endemic in over 100 countries. IgM ELISA identifies acute infection; IgG ELISA monitors vaccine-induced immunity. Increasingly relevant as the first licensed chikungunya vaccines enter post-marketing surveillance.

Chikungunya IgG ELISAChikungunya IgM ELISAVLP Vaccine Immunogenicity
View Chikungunya ELISA →
Yellow Fever (YFV)
Arboviral

Yellow Fever Virus is endemic across tropical Africa and South America. Live-attenuated 17D vaccine is highly effective but under-utilised. IgG ELISA (KBVH605, 30 ng/ml) measures post-vaccination protective antibody; IgM ELISA (KBVH606) identifies breakthrough acute infection in vaccinated populations.

KBVH605 IgG (30 ng/ml)KBVH606 IgM (30 ng/ml)WHO TRS-referenced
View Yellow Fever ELISA →
Japanese Encephalitis (JEV)
Arboviral

JEV is the leading cause of viral encephalitis in Asia, with an estimated 68,000 cases annually. Inactivated Vero cell-derived and live-attenuated vaccines require IgG titration ELISA and plaque reduction neutralisation support for immunogenicity endpoints. IgM ELISA confirms active infection in non-immune populations.

JEV IgG ELISAJEV IgM ELISAVaccine ImmunogenicityEndemic Region Serosurveillance
View JEV ELISA →
Rabies Virus
Rabies

Krishgen's five-assay rabies panel is among the most comprehensive available in ELISA format: glycoprotein antigen (KBVH177), nucleoprotein antigen (KBVH180), and three IgG antibody assays targeting subtypes 1, 2, 3 across both structural proteins. Covers pre-exposure prophylaxis monitoring, post-exposure serology, and vaccine potency assessment.

KBVH177 GP AntigenKBVH180 NP AntigenKBVH077 IgG (1,2,3)KBVH277 NP-IgGKBVH377 GP-IgG0–10 IU/ml • 6.25–200 U/ml
View Rabies panel →
Hepatitis B (HBV)
Hepatitis

HBV remains endemic across South and Southeast Asia with over 296 million chronic carriers globally. Anti-HBs titre ≥10 mIU/ml is the standard correlate of vaccine-induced protection. Krishgen's HBV panel covers all four major antigen and antibody targets used in vaccination monitoring and antiviral treatment assessment.

HBsAg ELISAAnti-HBs (HBsAb)HBeAg / Anti-HBeHBcAg / Anti-HBc IgM/IgG
View HBV ELISA →
Hepatitis C (HCV)
Hepatitis

HCV infects ~58 million people globally with no licensed vaccine. Anti-HCV antibody ELISA are used for seroprevalence studies and novel vaccine candidate evaluation in animal models. Antigen assays support viral load surrogate measurement and mechanism-of-action studies.

Anti-HCV IgG ELISAHCV Antigen ELISASeroprevalence / Cohort Studies
View HCV ELISA →
Influenza A & B
Respiratory

Annual influenza vaccination requires strain-specific and cross-reactive immunogenicity ELISA. Antibody assays for Influenza A (including H1N1, H3N2) and Influenza B measure post-vaccination seroconversion in serum and plasma — supporting seasonal and pandemic influenza vaccine evaluation programmes.

Influenza A Ab ELISAInfluenza B Ab ELISAH1N1 / H3N2Human Serum / Plasma
View Influenza ELISA →
RSV
Respiratory

RSV is the leading cause of lower respiratory tract infection in infants and immunocompromised adults. With prefusion F protein-based RSV vaccines now approved and entering widespread use, antigen and antibody ELISA support post-market immunogenicity monitoring and mechanistic research into protection correlates.

RSV Antigen ELISARSV IgG Antibody ELISAPrefusion F Protein Assays
View RSV ELISA →
SARS-CoV-2
Coronavirus

Krishgen's 50+ SARS-CoV-2 assay panel covers spike (S1, S2, RBD, whole spike), nucleocapsid, envelope, and membrane protein — in human, mouse, rat, hamster, and rabbit. Six surrogate virus neutralisation tests (sVNT) cover major variant lineages. Maintained for ongoing COVID-related and long-COVID research.

Spike S1 / S2 / RBD / N proteinIgG / IgM Quantitative TitrationsVNT — 6 Variants (BSL-2)Mouse / Rat / Hamster / Rabbit / Human
View SARS-CoV-2 assays →
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Assay Biology

Key Biomarkers & Antigens by Pathogen

Select a pathogen to explore the key antigens, antibody isotypes, and research applications covered by Krishgen's ELISA kits.

Dengue
Zika
Rabies
Hepatitis B
JEV / YFV
dsRNA / Innate Immunity
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Dengue Virus — NS1 Antigen, IgG, IgM & Serotype Biology

Dengue is caused by four antigenically distinct serotypes (DENV-1 through DENV-4); secondary heterotypic infection carries increased risk of severe dengue through antibody-dependent enhancement (ADE). ELISA-based serology distinguishes primary from secondary dengue, determines seroprevalence, and measures vaccine-induced immunity in tetravalent vaccine programmes. The NS1 antigen is secreted during the viraemic phase (days 1–5 post-onset) before IgM antibody responses develop — making it the ideal early diagnostic target. IgM peaks at 7–10 days; IgG persists long-term and is the primary immunogenicity endpoint in dengue vaccine trials.

NS1 Antigen ELISA
Secreted during viraemia; optimal days 1–5; early diagnostic window before seroconversion
Dengue IgM Antibody
Acute phase marker; peaks 7–10 days post-onset; primary infection indicator; fades within months
Dengue IgG Antibody
Convalescent / vaccine-induced; persists long-term; high titre at onset indicates secondary infection
Envelope / prM Protein
Primary target of type-specific neutralising antibodies; subunit vaccine antigen in clinical development
ADE Monitoring
IgG/NS1 patterns distinguish primary from secondary infection — critical for ADE risk stratification in trial cohorts
DENV Serotype 1–4
Pan-serotype coverage via cross-reactive antibody ELISA; serotype-specific assays available on request

Zika Virus — NS1, Envelope Protein & Congenital Zika Serology

Zika virus (ZIKV), a flavivirus closely related to dengue, causes congenital Zika syndrome including microcephaly. Serological cross-reactivity with dengue and other flaviviruses complicates diagnosis. Krishgen's NS1 ELISA (KBVH650, 50 pg/ml) provides antigen-based detection; the envelope protein ELISA (KBVH700, 180 pg/ml) supports vaccine antigen characterisation for subunit and mRNA vaccine candidates. Both are validated against the SPH2015 reference strain — the strain used in most active vaccine development programmes. IgG and IgM serology support seroprevalence studies in endemic populations and maternal cohort monitoring for congenital Zika risk assessment.

NS1 Antigen (KBVH650)
50 pg/ml sensitivity; strain SPH2015; acute viraemic phase detection in serum and plasma
Envelope Protein (KBVH700)
180 pg/ml; ZIKV-E protein characterisation; subunit vaccine antigen measurement
Zika IgG Antibody
Convalescent / long-term marker; seroprevalence and vaccine immunogenicity endpoint
Zika IgM Antibody
Acute infection; peaks within 1–2 weeks; detectable up to 12 weeks post-infection
Flavivirus Cross-reactivity
IgM window combined with NS1 specificity helps disambiguate Zika from co-circulating dengue in dual-endemic regions

Rabies Virus — Glycoprotein, Nucleoprotein & Post-Vaccination Serology

Rabies lyssavirus has a 100% case fatality rate once symptomatic. The WHO-recommended minimum protective titre post-vaccination is ≥0.5 IU/ml (by RFFIT). Krishgen's glycoprotein IgG ELISA (KBVH377) correlates with RFFIT neutralisation and is used for post-exposure prophylaxis (PEP) monitoring and pre-exposure prophylaxis (PrEP) titre verification in high-risk occupational cohorts (veterinarians, wildlife workers). The nucleoprotein IgG (KBVH277) detects cross-reactive antibody responses shared across lyssavirus genotypes, supporting research into cross-clade protection. Antigen assays (KBVH177, KBVH180) at 0–10 IU/ml quantify viral protein content in vaccine lots and research preparations.

Glycoprotein Antigen (KBVH177)
0–10 IU/ml; primary vaccine antigen; target of virus-neutralising antibodies
Nucleoprotein Antigen (KBVH180)
0–10 IU/ml; conserved N protein; cross-reactive across lyssavirus genotypes
IgG — Subtypes 1,2,3 (KBVH077)
6.25–200 U/ml; pan-subtype antibody; PEP and PrEP serology monitoring
IgG to Nucleoprotein (KBVH277)
6.25–200 U/ml; N protein-specific IgG; cross-clade protection research
IgG to Glycoprotein (KBVH377)
6.25–200 U/ml; correlates with RFFIT; primary seroprotection endpoint for rabies vaccination programmes

Hepatitis B — Antigen & Antibody Serology Panel

With over 296 million chronic HBV carriers globally and the highest burden in South and Southeast Asia, hepatitis B ELISA remain one of the most frequently requested serology tools in the region. Anti-HBs titre ≥10 mIU/ml is the universally accepted correlate of vaccine-induced protection — making quantitative HBsAb ELISA the primary vaccine immunogenicity endpoint for both primary and booster studies. HBsAg ELISA identify active infection; HBeAg positivity indicates high viral replication and infectivity; anti-HBc IgM distinguishes acute from chronic infection. All markers together constitute the standard hepatitis B serology panel used in clinical trial cohorts and programme evaluation.

HBsAg (Surface Antigen)
Primary marker of active HBV infection; vaccine target antigen; clearance = treatment response endpoint
Anti-HBs (HBsAb)
Vaccine-induced protective antibody; ≥10 mIU/ml = seroprotection; quantitative titration ELISA
HBeAg / Anti-HBe
Viral replication marker; e-antigen seroconversion is a key antiviral therapy endpoint in chronic HBV
HBcAg / Anti-HBc IgM
Core antigen; anti-HBc IgM = acute infection; IgG = past or chronic exposure

Japanese Encephalitis (JEV) & Yellow Fever Virus (YFV)

JEV is endemic across 24 Asian countries and causes approximately 68,000 cases of viral encephalitis annually, with a 30% case fatality rate and 50% long-term neurological sequelae in survivors. Multiple inactivated and live-attenuated vaccines are WHO-prequalified; immunogenicity ELISA measuring JEV IgG seroconversion and long-term antibody persistence are standard endpoints in vaccine programme evaluation across high-burden countries. Yellow Fever is endemic in 47 countries in Africa and the Americas — live-attenuated 17D vaccine confers lifelong immunity in most recipients. YFV IgG ELISA (KBVH605, 30 ng/ml) and IgM ELISA (KBVH606, 30 ng/ml) support post-vaccination surveillance and outbreak serosurveys. Both JEV and YFV assays are validated per WHO TRS guidance for relevant arboviral vaccines and ICH Q2(R2)/Q14.

JEV IgG Antibody ELISA
Long-term seroconversion endpoint; primary immunogenicity measure in JE vaccine trials
JEV IgM Antibody ELISA
Acute encephalitis serology; IgM in CSF confirms acute JEV in non-immune individuals
YFV IgG (KBVH605)
30 ng/ml sensitivity; live-attenuated 17D vaccine immunogenicity; post-dose monitoring
YFV IgM (KBVH606)
30 ng/ml; acute YFV infection; breakthrough infection detection in vaccinated travellers
WHO TRS Alignment
Both assay families validated per WHO Technical Report Series for relevant arboviral vaccines

dsRNA ELISA — Viral Replication Marker, Innate Immune Sensing & mRNA Vaccine QC

Double-stranded RNA (dsRNA) is an obligate intermediate in the replication cycle of all RNA viruses — including every tropical pathogen on this page: Dengue, Zika, Chikungunya, Yellow Fever, JEV, Influenza, RSV, and SARS-CoV-2. As a non-self molecular pattern, dsRNA is recognised by innate immune sensors — TLR3 (endosomal), MDA5 and RIG-I (cytosolic) — triggering type I interferon (IFN-α/β) production and downstream antiviral gene expression. The KRIBIOLISA™ dsRNA J2 ELISA (KBBA56) uses the well-validated J2 anti-dsRNA monoclonal antibody to quantify dsRNA in infected cells, lysates, and tissue samples. It is a standard tool in antiviral drug discovery screening (measuring reduction in dsRNA as a proxy for viral replication inhibition) and in innate immunity research characterising viral evasion of dsRNA sensing. A second critical application is mRNA vaccine manufacturing QC — dsRNA is an immunostimulatory contaminant generated during in vitro transcription (IVT) of mRNA, known to trigger innate responses that reduce mRNA translation efficiency and can contribute to adverse reactogenicity. Accurate dsRNA quantification is therefore essential in the mRNA vaccine production workflow.

KBBA56 dsRNA J2 ELISA
J2 monoclonal antibody-based; detects dsRNA ≥40 bp; validated in cell lysates and purified RNA preparations
RNA Virus Replication Marker
dsRNA produced during replication of Dengue, Zika, CHIKV, Influenza, RSV, SARS-CoV-2, JEV — all negative-sense and positive-sense RNA viruses
TLR3 / MDA5 / RIG-I Pathway
Pattern recognition receptors sensing dsRNA; TLR3 (endosomal), MDA5 preferentially senses long dsRNA, RIG-I short dsRNA with 5'-triphosphate
IFN-β / Innate Sensing Research
dsRNA-induced IRF3 phosphorylation drives IFN-β transcription; ELISA supports pathway activation studies alongside cytokine readouts
Antiviral Drug Screening
dsRNA quantification as pharmacodynamic biomarker for antiviral efficacy — reduced dsRNA signal indicates inhibition of viral replication
mRNA Vaccine Manufacturing QC
dsRNA contamination in IVT-derived mRNA reduces translation and increases innate reactogenicity; dsRNA ELISA is a critical release assay in mRNA vaccine production
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Product Tables

KRIBIOLISA™ & GENLISA™ Assay Listing

Click any category to expand the full assay listing. All kits: 1 × 96-well break-apart, ISO 13485-manufactured. For current pricing (USD/INR/GBP) or availability (standard 3–4 weeks lead time), contact info@krishgen.com.

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Arboviral ELISA — Dengue • Zika • Chikungunya • Yellow Fever • JEV

IgG • IgM • NS1 Antigen • Envelope Protein • Serum / Plasma
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All arboviral ELISA are validated in human serum and plasma as primary matrices. NS1 antigen and envelope protein assays are additionally validated in cell culture supernatant. WHO TRS guidance for relevant arboviral vaccines is referenced in validation documentation. Contact technical@krishgen.com for cross-reactivity data between co-endemic flaviviruses (Dengue, Zika, JEV, YFV).

Cat NoAssay NameTarget / FormatSensitivity / Range
Dengue Virus (DENV 1–4)
DENV-IgGDengue IgG Antibody ELISAIgG Serology • DENV 1–4Quantitative
DENV-IgMDengue IgM Antibody ELISAIgM Acute InfectionQualitative
DENV-NS1Dengue NS1 Antigen ELISANS1 Antigen • Early Viraemic PhaseQualitative / Quantitative
Zika Virus (ZIKV — Strain SPH2015)
KBVH650Zika Virus NS1 ELISANS1 Antigen • Strain SPH201550 pg/ml
KBVH700Zika Virus Envelope Protein (ZIKV-E) ELISAE Protein • Vaccine Antigen Characterisation180 pg/ml
ZIKV-IgGZika IgG Antibody ELISAIgG Serology • SeroprevalenceQualitative
ZIKV-IgMZika IgM Antibody ELISAIgM Acute InfectionQualitative
Chikungunya Virus (CHIKV)
CHIKV-IgGChikungunya IgG Antibody ELISAIgG • Convalescent / Vaccine ImmunityQualitative
CHIKV-IgMChikungunya IgM Antibody ELISAIgM • Acute Alphavirus InfectionQualitative
Yellow Fever Virus (YFV)
KBVH605Yellow Fever Virus IgG ELISAIgG • Vaccine Immunogenicity30 ng/ml
KBVH606Yellow Fever Virus IgM ELISAIgM • Acute Infection Marker30 ng/ml
Japanese Encephalitis Virus (JEV)
JEV-IgGJapanese Encephalitis IgG ELISAIgG Serology • Vaccine ImmunogenicityQualitative
JEV-IgMJapanese Encephalitis IgM ELISAIgM • Acute Encephalitis ConfirmationQualitative

Rabies Virus — 5-Assay Panel (Glycoprotein & Nucleoprotein)

Antigen + IgG Antibody • 0–10 IU/ml & 6.25–200 U/ml • Human
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Krishgen's five-assay rabies panel is one of the most comprehensive ELISA offerings available for rabies vaccine research. Antigen assays quantify glycoprotein and nucleoprotein viral protein content (0–10 IU/ml using WHO reference calibrators). Antibody assays measure post-vaccination IgG across subtypes 1, 2, and 3 in the 6.25–200 U/ml range — spanning both protein targets.

Cat NoAssay NameTargetRange
Rabies Antigen Assays
KBVH177Rabies Glycoprotein Antigen ELISAG Protein Antigen • Vaccine Antigen Quantification0–10 IU/ml
KBVH180Rabies Nucleoprotein Antigen ELISAN Protein Antigen • Cross-Reactive Antigen0–10 IU/ml
Rabies IgG Antibody Assays
KBVH077Rabies IgG Antibody ELISA — Subtypes 1, 2, 3Pan-subtype IgG • PEP / PrEP Serology6.25–200 U/ml
KBVH277Rabies IgG Antibody to Nucleoprotein ELISAN Protein-Specific IgG • Cross-Clade Research6.25–200 U/ml
KBVH377Rabies IgG Antibody to Glycoprotein ELISAG Protein-Specific IgG • Correlates with RFFIT6.25–200 U/ml

Hepatitis B & C • Influenza • RSV • VZV • HIV — Respiratory & Systemic Viral ELISA

HBV • HCV • Influenza A/B • RSV • VZV IgG/IgM • HIV
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Core serological and antigen ELISA for the most researched non-tropical infectious disease targets. All kits ISO 13485-manufactured with Gold Ring QC. For VZV IgG (KBVH601), full ICH Q5A/Q5D referenced documentation is available on request.

Cat NoAssay NameTargetFormat
Hepatitis B Virus (HBV)
HBsAg-ELISAHBsAg (Surface Antigen) ELISAActive HBV Infection MarkerQualitative
Anti-HBs-ELISAAnti-HBs (HBsAb) ELISAVaccine-Induced Protective AntibodyQuantitative
HBeAg-ELISAHBeAg ELISAViral Replication MarkerQualitative
Anti-HBc-ELISAAnti-HBc IgM / IgG ELISAAcute vs Past / Chronic Infection DifferentiatorQualitative
Hepatitis C Virus (HCV)
HCV-Ab-ELISAAnti-HCV IgG Antibody ELISAHCV Exposure / SeroprevalenceQualitative
HCV-Ag-ELISAHCV Antigen ELISAViral Protein DetectionQualitative
Influenza A & B
INFA-AbInfluenza A Antibody ELISA (H1N1, H3N2)Influenza A IgG • Post-Vaccination SerologyQualitative
INFB-AbInfluenza B Antibody ELISAInfluenza B IgG • Seasonal Vaccine MonitoringQualitative
RSV • VZV
RSV-AgRSV Antigen ELISARSV Antigen Detection • Prefusion F ResearchQualitative
KBVH601Varicella-Zoster Virus IgG ELISA (VZV-IgG)VZV IgG • Varicella / Shingles Vaccine Immunogenicity8 ng/ml
KBVH602Varicella-Zoster Virus IgM ELISA (VZV-IgM)VZV IgM • Primary Infection / Acute SeroconversionQualitative

Vaccine Manufacturing QC — CRM197 Carrier Protein Quantification

KBVH500 • 5 µg/ml LOD • Conjugate / Toxoid / Polysaccharide Vaccine • WHO TRS • ICH Q2(R2)/Q14
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CRM197 (Cross-Reacting Material 197) is the most widely used carrier protein in licensed glycoconjugate vaccines — including those against Streptococcus pneumoniae, Neisseria meningitidis, Haemophilus influenzae type b, and Salmonella typhi Vi. Quantifying CRM197 content during conjugation, purification, and final product release ensures batch consistency and supports in-process control. KBVH500 is validated against Fina Biosolutions EcoCRM™ (the reference material used by leading vaccine manufacturers) and has been tested for compatibility with polysaccharide-conjugated matrices. For samples containing high antigen load, polysaccharide-conjugates, or adjuvant, spike-recovery and dilution linearity evaluation is recommended before study use.

Cat NoAssay NameApplicationRange / LOD
KBVH500KRIBIOLISA™ CRM197 Carrier Protein Quantification ELISAIn-process QC • Final product release • Conjugation monitoring • Comparability studies5 µg/ml LOD

dsRNA ELISA — Viral Replication, Innate Immune Sensing & mRNA Vaccine QC

KBBA56 • J2 Antibody • TLR3 / MDA5 / RIG-I • mRNA Vaccine Manufacturing • Antiviral Drug Screening
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The KRIBIOLISA™ dsRNA J2 ELISA (KBBA56) uses the well-validated J2 monoclonal antibody to detect and quantify double-stranded RNA ≥40 bp in cell lysates, tissue homogenates, and purified RNA preparations. dsRNA is produced as an obligate replication intermediate by all RNA viruses — making it a universal viral replication biomarker applicable across every tropical pathogen in this catalogue. The J2 antibody is the gold-standard reagent for dsRNA detection in innate immunity research and is increasingly used in mRNA vaccine manufacturing QC to measure dsRNA contamination generated during in vitro transcription (IVT), where dsRNA reduces mRNA translation efficiency and contributes to innate reactogenicity.

Cat NoAssay NameApplicationDetection
KBBA56KRIBIOLISA™ dsRNA J2 ELISAViral replication marker • Innate immune sensing research • mRNA vaccine IVT dsRNA contaminant QC • Antiviral drug screening (pharmacodynamic biomarker)dsRNA ≥40 bp • Cell lysates / Purified RNA
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ISO 13485 Certified. Gold Ring QC. Trusted by Vaccine Manufacturers across Asia, Africa and Latin America.

Krishgen is a dedicated ELISA manufacturer — not a distributor. All kits are produced in ISO 13485 and CDSCO-certified Class 7/8 cleanrooms in Mumbai and California. Every assay is validated against Krishgen's seven-point "Gold Ring" QC protocol: lot-to-lot consistency, dilutional linearity, recovery, intra- and inter-assay precision, stability, and sensitivity. This ensures results are reproducible across both research sites and production batches — critical for multi-site serosurveillance studies and vaccine lot release programmes.

Our rabies panel (5 assays) is one of the most complete commercially available ELISA offerings for the target, covering both viral structural protein antigens and three distinct antibody measurement formats. Our arboviral portfolio — spanning Dengue, Zika, Chikungunya, Yellow Fever, and JEV — is built for the practical realities of research in dual-endemic regions, with cross-reactivity characterisation available on request.

For vaccine manufacturing applications, the KRIBIOLISA™ CRM197 ELISA has been validated against Fina Biosolutions EcoCRM™ and tested for compatibility with polysaccharide-conjugated matrices across multiple conjugate vaccine programmes. The dsRNA J2 ELISA (KBBA56) adds a cross-cutting innate immunity layer — applicable across every RNA virus in this catalogue and to mRNA vaccine manufacturing QC.

Frequently Asked Questions

Do your Dengue ELISA cross-react with Zika or JEV?
Flavivirus cross-reactivity is a documented challenge in dual-endemic regions. Krishgen characterises cross-reactivity between co-circulating flaviviruses (Dengue, Zika, JEV, YFV) in our validation data. Contact info@krishgen.com for kit-specific cross-reactivity data before ordering for studies in regions with co-endemic flaviviruses.
What is the difference between KBVH077 and KBVH377 for rabies?
KBVH077 measures total rabies IgG across subtypes 1, 2, and 3 — providing a pan-subtype antibody readout. KBVH377 is specific to glycoprotein-targeted IgG, which correlates most closely with RFFIT (rapid fluorescent focus inhibition test) neutralising titres — the WHO gold standard for rabies vaccine immunogenicity. For post-vaccination seroprotection monitoring, KBVH377 is the preferred assay.
Are the Zika ELISA (KBVH650 / KBVH700) validated for cell culture samples?
Yes. Both the NS1 (KBVH650) and envelope protein (KBVH700) Zika assays are validated in serum, plasma, and cell culture supernatant. Both are validated for strain Zika SPH2015. For samples from other Zika strains, cross-reactivity confirmation is recommended — contact info@krishgen.com.
Is the CRM197 ELISA validated for polysaccharide-conjugated samples?
KBVH500 is validated for serum, plasma, cell culture supernatant, and PBS 7.4 buffer. For polysaccharide-conjugate-containing matrices, dilution in sample diluent is recommended to minimise matrix effects. High adjuvant concentration, organic solvents, or strong chaotropes may affect recovery — evaluate with spike-recovery and dilution linearity before study use.
What is the dsRNA J2 ELISA (KBBA56) used for in infectious disease research?
The dsRNA J2 ELISA quantifies double-stranded RNA using the well-validated J2 monoclonal antibody. It has two primary applications in infectious disease research: (1) as a universal RNA virus replication marker — dsRNA is produced during replication of Dengue, Zika, CHIKV, Influenza, SARS-CoV-2 and all other RNA viruses, making it useful for antiviral drug screening (reduced dsRNA = inhibited replication) and innate immune sensing studies; and (2) as a QC assay in mRNA vaccine manufacturing, where dsRNA is an immunostimulatory contaminant generated during in vitro transcription that reduces mRNA translation efficiency. Contact info@krishgen.com for validation data.

Custom Services & Specialist Enquiries

Krishgen's in-house manufacturing capability means we can develop novel viral antigen or antibody ELISA to order, validate in non-standard matrices, or provide Genbulk™ packs for high-throughput serosurveillance and vaccine lot release programmes.

Need a Specific Pathogen or Matrix Validation?

Krishgen manufactures infectious disease ELISA across 15+ virus families. Our technical team can identify the right assay, confirm cross-reactivity and matrix validation data, or custom-develop a new kit for your target pathogen or study design.