Rat SPI1(Spleen Focus Forming Virus Proviral Integration Oncogene) ELISA Kit

 

Rat SPI1(Spleen Focus Forming Virus Proviral Integration Oncogene) ELISA Kit

Size

96T

Catalog no.

ELK8056

Price

608 EUR

Buy at gentaur.com
Assay length

3h

Tissue

spleen

Standard

20ng/mL

Assay Type

Sandwich

Sensitivity

0.116ng/mL

Detection range

0.312-20ng/mL

Research Area

Tumor immunity;

Latin name

Rattus norvegicus

Test

ELISA Enzyme-linked immunosorbent assays Code 90320007 SNOMED

Properties

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

Alternative Names

OF; PU.1; SFPI1; SPI-1; SPI-A; SPI-1 Proto-Oncogene; Hematopoietic Transcription Factor PU.1; 31 kDa Transforming Protein

About

Rats are used to make rat monoclonal anti mouse antibodies. There are less rat- than mouse clones however. Rats genes from rodents of the genus Rattus norvegicus are often studied in vivo as a model of human genes in Sprague-Dawley or Wistar rats.

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 Spleen Focus Forming Virus Proviral Integration Oncogene (SPI1). Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody specific to Spleen Focus Forming Virus Proviral Integration Oncogene (SPI1). 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 Spleen Focus Forming Virus Proviral Integration Oncogene (SPI1), 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 Spleen Focus Forming Virus Proviral Integration Oncogene (SPI1) in the samples is then determined by comparing the O.D. of the samples to the standard curve.