Mouse HINT2(Histidine Triad Nucleotide Binding Protein 2) ELISA Kit

 

Mouse HINT2(Histidine Triad Nucleotide Binding Protein 2) ELISA Kit

Size

96T

Catalog no.

ELK7153

Price

608 EUR

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Assay length

3h

Standard

10ng/mL

Assay Type

Sandwich

Sensitivity

0.061ng/mL

Latin name

Mus musculus

Detection range

0.156-10ng/mL

Research Area

Signal transduction;

Alternative Names

HIT-17kDa; PKCI-1-related HIT protein

Properties

E05 478 566 350 170 or Enzyme-Linked Immunosorbent Assays,E05 478 566 350 170 or Enzyme-Linked Immunosorbent Assays

Test

ELISA Enzyme-linked immunosorbent assays Code 90320007 SNOMED,Mouse or mice from the Mus musculus species are used for production of mouse monoclonal antibodies or mabs and as research model for humans in your lab. Mouse are mature after 40 days for females and 55 days for males. The female mice are pregnant only 20 days and can give birth to 10 litters of 6-8 mice a year. Transgenic, knock-out, congenic and inbread strains are known for C57BL/6, A/J, BALB/c, SCID while the CD-1 is outbred as strain.

Test principle

The test principle applied in this kit is Sandwich enzyme immunoassay. The microtiter plate provided in this kit has been pre-coated with an antibody specific to Histidine Triad Nucleotide Binding Protein 2 (HINT2). Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody specific to Histidine Triad Nucleotide Binding Protein 2 (HINT2). Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain Histidine Triad Nucleotide Binding Protein 2 (HINT2), biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of Histidine Triad Nucleotide Binding Protein 2 (HINT2) in the samples is then determined by comparing the O.D. of the samples to the standard curve.