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Creative Biolabs
Product

Human RAC-alpha serine/threonine-protein kinase(AKT1) ELISA kit

[CAT#: NRZP-0722-ZP241]

For the quantitative determination of human RAC-alpha serine/threonineprotein kinase (AKT1) concentrations in serum, plasma, cell lysates.

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Product Overview

Description

This assay has high sensitivity and excellent specificity for detection of human AKT1.

Species Reactivity

Human

Marker

v-akt murine thymoma viral oncogene homolog 1

Principle

This assay employs the quantitative sandwich enzyme immunoassay technique. Antibody specific for AKT1 has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and any AKT1 present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conjugated antibody specific for AKT1 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 AKT1 bound in the initial step. The color development is stopped and the intensity of the color is measured.
Properites

Sensitivity

0.078 ng/ml

Detection Method

Sandwich

Sample Type

serum, plasma, cell lysates

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

0.312 ng/ml-20 ng/ml

Max Emission

450 nm
Target Details

Target

AKT1

Official Name

AKT1

Full Name

AKT serine/threonine kinase 1

Alternative Names

AKT; PKB; RAC; PRKBA; PKB-ALPHA; RAC-ALPHA

Gene ID

207(Human)

Uniprot ID

P31749(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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