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Creative Biolabs
Product

Rat Vitamin D3 receptor(VDR) ELISA kit

[CAT#: NRZP-0722-ZP266]

For the quantitative determination of bovine vascular endothelial growth factor A (VEGFA) concentrations in serum, plasma, tissue homogenates.

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Product Overview

Description

This assay has high sensitivity and excellent specificity for detection of bovine VEGFA.

Species Reactivity

Rat

Marker

Vitamin D (1,25- dihydroxyvitamin D3) receptor

Principle

This assay employs the quantitative sandwich enzyme immunoassay technique. Antibody specific for VEGFA has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and any VEGFA present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conjugated antibody specific for VEGFA 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 VEGFA bound in the initial step. The color development is stopped and the intensity of the color is measured.
Properites

Sensitivity

7.8 pg/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

31.2 pg/ml-2000 pg/ml

Max Emission

450 nm
Target Details

Target

VDR

Official Name

VDR

Full Name

vitamin D receptor

Alternative Names

NR1I1, vitamin D (1,25-dihydroxyvitamin D3) receptor; PPP1R163

Gene ID

24873(Rat)

Uniprot ID

P13053(Rat)
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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