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Creative Biolabs
Product

Human platelet membrane glycoprotein Ⅳ, GP-Ⅳ ELISA Kit

[CAT#: NRZP-0722-ZP275]

For the quantitative determination of human platelet membrane glycoprotein Ⅳ (GP-Ⅳ) concentrations in serum, plasma, tissue homogenates.

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Product Overview

Description

This assay has high sensitivity and excellent specificity for detection of human GP-Ⅳ.

Species Reactivity

Human

Marker

CD36 molecule (thrombospondin receptor)

Principle

This assay employs the quantitative sandwich enzyme immunoassay technique. Antibody specific for GP-Ⅳ has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and any GP-Ⅳ present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conjugated antibody specific for GP-Ⅳ is added to the wells. After washing, avidin conjugated Horseradish Peroxidase (HRP) is added to the wells. Following a wash to remove any unbound avidin-enzyme reagent, a substrate solution is added to the wells and color develops in proportion to the amount of GP-Ⅳ bound in the initial step. The color development is stopped and the intensity of the color is measured.
Properites

Sensitivity

0.625 ng/ml

Detection Method

Sandwich

Sample Type

serum, plasma, tissue homogenates

Assay Type

quantitative

Assay Time

3-5 working days

Assay Duration

1-5h

Precision

Intra-assay Precision (Precision within an assay): CV%<8%.
Three samples of known concentration were tested twenty times on one plate to assess.
Inter-assay Precision (Precision between assays): CV%<10%.
Three samples of known concentration were tested in twenty assays to assess.

Number Of Samples

50-100ul

Detection Range

2.5 ng/ml-160 ng/ml

Max Emission

450 nm
Target Details

Target

CD36

Official Name

CD36

Full Name

CD36 molecule

Alternative Names

FAT; GP4; GP3B; GPIV; CHDS7; PASIV; SCARB3; BDPLT10

Gene ID

948(Human)

Uniprot ID

P16671(Human)
Protocols

Protocols

1.Prepare reagents, samples and standards as instructed.
2.Add 100ul standard or sample to each well. lncubate 2 hours at 37°°C.
3.Remove the liquid of each well, don't wash.
4.Add 100ul Biotin-antibody(1x) to each well. Incubate 1 hour at 37°C.
5.Aspirate and wash 3 times.
6.Add 100ul HRP-avidin (1x) to each well.Incubate 1 hour at 37°°C.
7.Aspirate and wash 5 times.
8.Add 90ul TMB Substrate to each well.Incubate 15-30 minutes at 37°°C. Protect from light.
9.Add 50ul Stop Solution to each well.Read at 450 nm within 5 minutes.
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For Research Use Only. Not For Clinical Use.
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