KRIBIOLISA™ Blinatumomab (BLINCYTO) ELISA

SKU: KBI1197 Category:

58,000.00

Enzyme Immunoassay for the estimation of Blinatumomab in serum and plasma.

About the kit:
– Uses anti-idiotypic monoclonal antibodies which ensures higher specificity, and low cross reactivity.
– Recovery rates are between 85 – 115%
– Validated as per US FDA guidelines for Bioassays
– Precision CV<10%


Availability: 3 – 4 weeks | Pack Size: 1 x 96 wells



Description

Background:
Blinatumomab, marketed under the brand name BLINCYTO, is a monoclonal antibody used in the treatment of certain types of leukemia. It is specifically designed to target and bind to both CD19, a protein found on the surface of B cells, and CD3, a protein on the surface of T cells. Blinatumomab brings these immune cells into close proximity, facilitating the destruction of B cells by the activated T cells. BLINCYTO is approved for the treatment of Philadelphia chromosome-negative relapsed or refractory B-cell precursor acute lymphoblastic leukemia (ALL) in both pediatric and adult patients. This immunotherapy has demonstrated efficacy in patients who have not responded to other treatments or have experienced relapse, offering a novel approach to the management of this aggressive form of leukemia by harnessing the immune system’s ability to target and eliminate cancer cells

Additional information

Sample Type

Serum (100 ul), EDTA Plasma (100 ul), Heparin Plasma (100 ul), Citrate Plasma (100 ul)

Calibration Range

0 ng/ml – 2000 ng/ml

Specificity

80% – 120% to Blinatumomab

Cross Reactivity

< 0.5% cross-reactivity observed with related biomarker.

Interference

No significant interference observed with available related molecules.

Regulatory Status

Research Use Only

Research Area

Biosimilars / Therapeutic Drug Monitoring

Entez Gene ID

AMG103 Human

Alternate Names / Synonyms

Blinatumomab

Storage Temperature

Store the unopened product at 2-8C. Do not use past expiration date.

Validation

The kit uses a biosimilar research grade standard / calibrator. The standard / calibrator has been validated against WHO/NIBSC standard and/or against commercially sourced innovator drug where available. Please refer the IFU for more details.

Disclaimer

Trade name indicated is for reference purposes only. It does not reflect any licences or patent usage. The tradename is the registered trademark of the respective owners only.

Long Name

Protein Based Therapies – Monoclonal Antibody