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Cancer Biomarker ELISA - HER2, VEGF, PSA, CA-125, CEA, Mesothelin, MMP, HIF-1a | Krishgen Biosystems
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Cancer Research - Tumour Biomarker ELISA

Cancer
Biomarker
ELISA

Quantitative ELISA kits for soluble tumour biomarkers, angiogenesis markers, invasion and metastasis proteins, tumour hypoxia, and cancer stem cell markers - spanning 16+ tumour types and 200+ targets. Human, Mouse, and Rat validated. ISO 13485 manufactured.

Browse Assay Table Biomarker Science
16+
Tumour Types Covered
200+
Cancer Biomarker Targets
3+
Species per Target
<10%
CV - All Kits

Soluble Cancer Biomarkers - Why ELISA

Research Context

IHC establishes protein expression in tissue - ELISA quantifies soluble biomarkers in circulation. Many cancer-associated proteins are shed, secreted, or cleaved from cell surfaces into serum, plasma, ascites fluid, or urine, where they are measurable at nanogram-to-picogram concentrations. Quantitative ELISA of these soluble forms enables non-invasive longitudinal monitoring of tumour burden, disease progression, therapy response, and metastatic spread - applications that tissue-based methods cannot address.

Cancer biomarkers serve distinct roles depending on clinical context. Understanding the category your target falls into determines the right assay format and statistical interpretation.

Diagnostic
Tumour Detection
Distinguish cancer from benign conditions. Examples: PSA (prostate), CA-125/MUC16 (ovarian), CEA (CRC), AFP (HCC). Typically measured in serum; sensitivity and specificity define clinical utility.
Prognostic
Disease Outcome
Predict outcome independent of treatment. Examples: soluble HER2 ECD (breast), VEGF (angiogenic tumours), MMP2/9 (metastatic potential), HIF-1a (hypoxic tumours). High expression = poor prognosis in most cases.
Predictive
Therapy Response
Predict response to a specific treatment. Examples: sPD-L1 (anti-PD-1 therapy), HER2 (trastuzumab eligibility), sBCMA (anti-BCMA therapy). Typically paired with drug PK ELISA for full PK/PD profiling.
Pharmacodynamic
Biological Activity
Confirm on-target drug activity. Examples: VEGF (bevacizumab), soluble E-Cadherin (EMT inhibitors), ALDH1A1 (CSC-targeted agents). Changes pre/post treatment indicate mechanism engagement.
Key Soluble Biomarkers by Tumour Type
Cancer TypePrimary DiagnosticPrognostic / PD MarkersTherapy-Linked
Lung (NSCLC)-VEGF - MMP2 - HIF-1asPD-L1 - sPD-1
BreastsHER2 ECDVEGF - E-Cadherin - ALDH1A1sHER2 - sPD-L1
ColorectalCEA - AFPVEGF - MMP9 - STAT3VEGF - sPD-1
ProstatePSA - PSMAVEGF - STAT3PSMA - sPD-L1
OvarianCA-125 - HE4VEGF - IL-6 - MesothelinVEGF - sPD-L1
PancreaticCA 19-9 - MesothelinVEGF - HIF-1a - MMP2CD40 - sPD-L1
HepatocellularAFPVEGF - MMP9 - TGF--1VEGF - sPD-1

Validated ELISA by Tumour Type

Core soluble biomarker ELISA for the six most researched solid tumour types. All kits validated in human serum and plasma; mouse and rat reactivity available for the majority of targets for use in xenograft and syngeneic pre-clinical models.

Lung Cancer
NSCLC - SCLC

VEGF (KB1155) is the primary angiogenesis marker and bevacizumab combination target. Soluble PD-L1 (KBBA52) and PD-1 (KBBA50) are predictive biomarkers for pembrolizumab eligibility in NSCLC. HIF-1a elevation marks hypoxic tumours with upregulated PD-L1 and poor prognosis. MMP2 quantifies invasive and metastatic potential.

VEGF - KB1155 sPD-L1 - KBBA52 HIF-1a MMP2 / MMP9 LAG-3 TIGIT
Browse Lung Cancer ELISA
Breast Cancer
HR+ - HER2+ - TNBC

Soluble HER2 ECD (extracellular domain) is shed into serum during HER2+ disease and is measurable as a treatment response biomarker. VEGF and VEGFR2 drive angiogenesis in all subtypes. ALDH1A1 marks cancer stem cell populations particularly relevant in TNBC. E-Cadherin loss is the key EMT event in metastatic lobular carcinoma.

sHER2 ECD VEGF - KB1155 ALDH1A1 E-Cadherin sPD-L1 - KBBA52 LAG-3
Browse Breast Cancer ELISA
Colorectal Cancer
CRC - Metastatic

CEA is the primary serum biomarker for CRC surveillance and treatment monitoring. VEGF (KB1155) is the bevacizumab and ramucirumab target; VEGFR2 (KBH4535) is the ramucirumab receptor. MMP9 marks invasive capacity and correlates with liver metastasis risk. STAT3 (KBH0650) downstream of IL-6 drives cetuximab resistance.

CEA VEGF - KB1155 VEGFR2 - KBH4535 MMP9 STAT3 - KBH0650
Browse CRC ELISA
Prostate Cancer
Localised - mCRPC

PSA is the most widely used serum biomarker for prostate cancer detection and post-treatment monitoring. PSMA expression increases with tumour grade and is the target for 177Lu-PSMA-617 RLT. Soluble VEGF is significantly elevated in prostatic carcinoma vs benign hyperplasia. STAT3 and IL-6 drive castration-resistant progression in mCRPC.

PSA PSMA VEGF - KB1155 STAT3 - KBH0650 IL-6 - KBH8009
Browse Prostate Cancer ELISA
Ovarian Cancer
HGSC - Mucinous

CA-125 (MUC16) is the primary serum biomarker for ovarian cancer monitoring and recurrence detection. HE4 is used alongside CA-125 in the ROMA algorithm for early detection. VEGF-A is the bevacizumab target in ICON7/GOG-0218 - measurable in ascites and serum. Mesothelin is elevated in HGSC and is an emerging therapeutic target.

CA-125 / MUC16 HE4 VEGF - KB1155 Mesothelin IL-6 - KBH8009
Browse Ovarian Cancer ELISA
Pancreatic Cancer
PDAC - PanNET

CA 19-9 and Mesothelin are the primary serum biomarkers for PDAC. AFP distinguishes hepatoid PDAC from conventional adenocarcinoma. VEGF and HIF-1a mark the extensively vascularised and hypoxic stroma of PDAC. IL-6 and STAT3 signalling promotes tumour cell survival and resistance to chemotherapy in the PDAC microenvironment.

CA 19-9 Mesothelin AFP VEGF - KB1155 HIF-1a STAT3 - KBH0650
Browse Pancreatic Cancer ELISA

VEGF & Angiogenesis Biomarker ELISA

Tumour angiogenesis - driven primarily by VEGF - is required for tumours to grow beyond 1-2 mm- and is the mechanism exploited by bevacizumab, ramucirumab, and multi-kinase inhibitors. Krishgen's VEGF ELISA (KB1155) is one of the most widely cited assays in the catalogue, available in 7+ species for seamless translation from pre-clinical models to clinical samples.

VEGF
Master Angiogenesis Regulator

Vascular endothelial growth factor A (VEGF-A) is the primary driver of tumour neovascularisation. Serum VEGF is elevated in most solid tumours and correlates with tumour stage, metastatic spread, and poor prognosis. It is the direct target of bevacizumab and the upstream driver of ramucirumab target VEGFR2.

KB1155Human - Mouse - Rat - Porcine - Bovine - Equine - Rabbit
KB1155 - View Datasheet
VEGFR2
Primary Signalling Receptor

VEGFR2 (KDR/Flk-1) is the primary signalling receptor for VEGF-A on endothelial cells, mediating proliferation, migration, and vascular permeability. It is the direct target of ramucirumab and is overexpressed on tumour vasculature. Soluble VEGFR2 in serum serves as a pharmacodynamic biomarker for anti-angiogenic therapy.

KBH4535Human - Mouse - Rat - Rabbit
KBH4535 - View Datasheet
MMP2 / MMP9
Matrix Metalloproteinases

MMP2 (gelatinase A) and MMP9 (gelatinase B) degrade collagen IV in the basement membrane and extracellular matrix, enabling tumour invasion and contributing to angiogenesis by releasing VEGF from ECM reservoirs. Elevated serum MMP2 and MMP9 correlate with metastatic disease and poor prognosis across lung, breast, colorectal, and ovarian cancers.

MMP2 ELISAMMP9 ELISAHuman - Mouse - Rat
View MMP ELISA

Epithelial-Mesenchymal Transition & Invasion Biomarkers

Epithelial-to-mesenchymal transition (EMT) is a staged process in which tumour cells lose epithelial polarity and acquire an invasive mesenchymal phenotype - the critical first step in distant metastasis. Quantitative ELISA of soluble EMT markers in serum and plasma enables non-invasive monitoring of metastatic potential without repeated tumour sampling.

E-Cadherin
Epithelial Integrity Marker

E-Cadherin maintains cell-cell adhesion at epithelial junctions. Loss of E-Cadherin expression is the canonical hallmark of EMT onset - triggered by transcription factors Snail, Slug, Twist, and ZEB1 downstream of TGF--, Wnt, and hypoxia. Soluble E-Cadherin fragments are shed into circulation and detectable by ELISA in breast, gastric, and colorectal cancer patients. Correlates with metastatic lobular breast carcinoma and lymph node involvement.

EMT onset markerMetastatic lobular BCHuman
View E-Cadherin ELISA
Vimentin
Mesenchymal Transition Marker

Vimentin is a type III intermediate filament protein characteristic of mesenchymal cells. Its expression is upregulated as E-Cadherin is downregulated during EMT. Elevated serum Vimentin correlates with advanced disease stage, lymph node metastasis, and reduced survival in lung, breast, and gastric cancers. Often used as the paired readout alongside E-Cadherin for a complete EMT biomarker assessment.

EMT mesenchymal markerLung - Breast - GastricHuman
View Vimentin ELISA

HIF-1a, ALDH1A1, CD44 & CD133 ELISA

Tumour hypoxia and cancer stem cell (CSC) biology are mechanistically linked - HIF-1a drives CSC maintenance, while CSC populations are preferentially located in hypoxic tumour niches. Both pathways drive therapy resistance, immune evasion, and tumour recurrence. Quantitative serum/plasma ELISA for these targets enables tracking of these aggressive phenotypes longitudinally without biopsy.

HIF-1a
Hypoxia Master Regulator

HIF-1a (Hypoxia-Inducible Factor 1-alpha) is the master transcription factor activated when tumour oxygen levels fall below ~1% (severe hypoxia). It drives expression of VEGF (angiogenesis), GLUT1 (metabolic reprogramming), and PD-L1 (immune evasion) - three of the most targetable pathways in oncology. Serum HIF-1a elevation correlates with advanced tumour stage and poor prognosis in NSCLC, RCC, breast, and pancreatic cancer. HIF-1a ELISA is validated in human serum and plasma; mouse reactivity available for pre-clinical models.

VEGF inductionPD-L1 upregulationNSCLC - RCC - BreastHu / Mouse
View HIF-1a ELISA
Cancer Stem Cell Markers
ALDH1A1 - CD44 - CD133

ALDH1A1 (aldehyde dehydrogenase 1A1) is a functional CSC marker - its enzymatic activity protects stem-like cells from oxidative damage and chemotherapy. Elevated in breast, lung, and colorectal CSC subpopulations. CD44 is a cell surface glycoprotein upregulated on CSCs across most solid tumour types; soluble CD44 in serum correlates with metastatic disease. CD133 (Prominin-1) marks CSC populations in colorectal, glioblastoma, HCC, and ovarian cancer and is strongly associated with chemotherapy resistance and tumour recurrence. All three available as ELISA in Human.

ALDH1A1 - CSC functionCD44 - Stemness / MetastasisCD133 - Therapy resistanceHuman
View Cancer Stem Cell ELISA

Cancer Biomarker ELISA - Full Table

All key cancer biomarker ELISA with species availability. Contact info@krishgen.com for catalogue numbers, pricing, and validation data.

Category Biomarker Clinical Role Species Assay
Angiogenesis VEGF-A Vascular Endothelial Growth Factor Bevacizumab target - Prognosis across solid tumours Hu - Mo - Ra - Porcine - Bovine - Equine KB1155
Angiogenesis VEGFR2 KDR / Flk-1 Ramucirumab target - Anti-angiogenic PD marker Hu - Mo - Ra - Rabbit KBH4535
Angiogenesis MMP2 Matrix Metalloproteinase-2 ECM invasion - Metastatic potential - Angiogenesis Hu - Mo - Ra Contact us
Angiogenesis MMP9 Matrix Metalloproteinase-9 Liver metastasis risk (CRC) - VEGF release from ECM Hu - Mo - Ra Contact us
Breast HER2 ECD Soluble ErbB2 / HER2 Treatment response monitoring - Trastuzumab eligibility Human Contact us
Colorectal CEA Carcinoembryonic Antigen CRC surveillance - Post-surgical monitoring Human Contact us
Liver / CRC AFP Alpha-Fetoprotein HCC diagnosis - Hepatoid tumour marker Hu - Mo - Ra Contact us
Prostate PSA Prostate Specific Antigen Prostate cancer screening - Post-treatment monitoring Human Contact us
Prostate PSMA Prostate Specific Membrane Antigen RLT target - mCRPC grading - High-grade disease Human Contact us
Ovarian CA-125 / MUC16 Primary ovarian cancer biomarker - Recurrence monitoring Human Contact us
Ovarian HE4 Human Epididymis Protein 4 ROMA algorithm (with CA-125) - Early detection Human Contact us
Ovarian / Pancreatic Mesothelin PDAC - HGSC - Mesothelioma - ADC target Human Contact us
Signalling STAT3 Signal Transducer & Activator IL-6 signalling - Cetuximab resistance - CRPC Hu - Porcine KBH0650
EMT E-Cadherin CDH1 EMT onset - Metastatic lobular breast cancer Human Contact us
EMT Vimentin VIM Mesenchymal transition - Invasion / metastasis Human Contact us
Hypoxia HIF-1a Hypoxia-Inducible Factor 1-alpha Hypoxia response - VEGF/PD-L1 induction - Poor prognosis Hu - Mouse Contact us
Cancer Stem Cells ALDH1A1 Aldehyde Dehydrogenase 1A1 CSC functional marker - Breast - Lung - CRC Human Contact us
Cancer Stem Cells CD44 Cluster of Differentiation 44 Stemness - Metastasis marker - Solid tumours Human Contact us
Cancer Stem Cells CD133 Prominin-1 Therapy resistance - CRC - GBM - HCC - Ovarian Human Contact us

Common Questions About Cancer Biomarker ELISA

Are these ELISA validated for ascites, pleural fluid, or tumour lysate
Most kits are validated in human serum and plasma as standard. Validation data for ascites, pleural fluid, BAL fluid, CSF, or tumour lysate is available for many targets on request - contact our technical team with your matrix and volume requirements.
Can the same ELISA kit be used for both patient serum and mouse xenograft samples
Not always - most cancer biomarker ELISA are species-specific. If you need to measure the same target in human and mouse samples from a xenograft study, you will need species-matched kits. We offer separate Human and Mouse kits for VEGF, STAT3, HIF-1a, and several other targets.
How is soluble HER2 (ECD) ELISA different from IHC HER2 scoring
IHC HER2 scoring (0-3+) measures receptor expression at the tissue level in a fixed, archived sample. Soluble HER2 ECD ELISA measures the cleaved extracellular domain shed into serum - a dynamic, longitudinal readout that changes with disease burden and response to trastuzumab or pertuzumab treatment.
What is the expected VEGF concentration range in patient serum
Serum VEGF is typically 100-1,000 pg/mL in healthy donors and 500-5,000+ pg/mL in cancer patients depending on tumour burden and vascularity. KB1155 covers this range; for very high-load samples, a standard dilution in sample diluent is recommended. Contact us for validated dilution guidance.
Are validation reports available for regulatory or publication purposes
Yes. Detailed validation guides covering dilutional linearity, spike recovery, freeze-thaw stability, intra- and inter-assay precision, and specificity are available for all catalogue kits. Request at sales1@krishgen.com. GLP-level validation for IND-enabling studies can be arranged through our custom services team.
Can you develop ELISA for cancer biomarkers not listed here
Yes. Krishgen's custom assay development team can design and validate ELISA for novel tumour targets, unusual sample matrices, or cancer-specific isoforms. Typical turnaround is 8-12 weeks from project initiation. Contact services@krishgen.com with your target and study design.

Can't Find Your Cancer Target?

Krishgen manufactures 20,000+ ELISA across 10+ species. Contact our team to find an existing assay or discuss custom development for your specific biomarker and matrix.

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