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CXCL11 (Human) ELISA Kit

A Sandwich ELISA kit for quantitative measurement of CXCL11

WARNING: This product can expose you to chemicals including Sulfuric acid and TMB, which are known to the State of California to cause cancer. For more information go to www.P65Warnings.ca.gov.
Catalog #: E5030
$750.00

Product Details

Cat # +Size E5030-100
Size 96 assays
Detection Method Absorbance is measured at 450 nm
Species Reactivity Human
Applications The ELISA kit is used for the quantitative detection of CXCL11 in serum, plasma, tissue homogenates and other biological fluids
Features & Benefits ● Assay Precision; Intra-Assay CV < 8% and Inter-Assay < 10%
● Sensitivity: 37.5 pg/ml
● Highly sensitive and specific
● Recovery Rate: 87-95% for serum, 85-100% for EDTA plasma and 89-105% for heparin plasma
● Detection range: 62.5-4000 pg/ml
Kit Components ● ELISA Microplate
● Wash Buffer (25X)
● Plate Sealers
● Lyophilized Standard (4 ng)
● Sample/Standard Dilution Buffer
● Biotin-labeled Antibody (Concentrated)
● Antibody Dilution Buffer
● HRP-Streptavidin Conjugate (SABC)
● SABC Dilution Buffer
● TMB Substrate
● Stop Solution
Storage Conditions 4°C
Shipping Conditions Gel Pack
USAGE For Research Use Only! Not For Use in Humans.

Details

CXCL11 (C-X-C motif chemokine 11) is a chemotactic cytokine strongly induced by interferon-gamma (IFN-γ). It binds to the chemokine receptor CXCR3. It plays an important role in pathophysiology of CNS diseases which involve T-cell recruitment. The levels of CXCL11 are increased in Sarcoidosis. BioVision’s CXCL11 (Human) ELISA Kit is used for the quantitative detection of CXCL11 in serum, plasma, tissue homogenates and other biological fluids. It is based on the principle of sandwich ELISA. The capture antibody is pre-coated on 96-well plates. The standards, test samples and biotin conjugated detection antibody are added to the wells subsequently, and washed with wash buffer. HRP-Streptavidin is added and unbound conjugates were washed away with wash buffer. The HRP enzymatic reaction is detected using TMB-substrate. Finally, an acidic stop solution terminates the enzymatic reaction. The color developed is directly proportional to the amount of CXCL11 in the sample.


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