Mouse Suppressor of cytokine signaling 5, Socs5 ELISA KIT

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  • Model: ELI-52274m
  • 20 Units in Stock
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Mouse SOCS5 ELISA KIT

Packing  96Tests

FOR RESEARCH USE ONLY; NOT FOR THERAPEUTIC OR DIAGNOSTIC APPLICATIONS! PLEASE READ ENTIRE PROCEDURE!

Gene Name  SOCS5

Protein Name  suppressor of cytokine signaling 5

Alternative Name

Mouse SOCS5 ELISA KIT , Mouse CIS6 ELISA KIT ,Mouse CISH6 ELISA KIT ,Mouse Cish5 ELISA KIT ,Mouse SOCS-5 ELISA KIT ,Mouse suppressor of cytokine signaling 5 ELISA KIT ,Mouse CIS-6 ELISA KIT ,Mouse cytokine-inducible SH2 protein 6 ELISA KIT ,Mouse cytokine-inducible SH2-containing protein 5 ELISA KIT

Intended use

Mouse SOCS5 ELISA KIT allows for the in vitro quantitative determination of SOCS5 concentrations in serum, plasma, tissue homogenates, cell culture supernates or other biological fluids.

 

Reagent

Quantity

Assay plate

1

Standard

2

Sample Diluent

1 × 20mL

Assay Diluent A

1 × 10mL

Assay Diluent B

1 × 10mL

Detection Reagent A

1 × 120μL

Detection Reagent B

1 × 120μL

Wash Buffer(25 x concentrate)

1 × 30mL

Substrate

1 × 10mL

Stop Solution

1 × 10mL

Plate sealer

5

 

Test principle      

The microtiter plate provided in Mouse SOCS5 ELISA KIT has been pre-coated with an SOCS5 antibody specific to SOCS5. Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody preparation specific for SOCS5 and then avidin conjugated to Horseradish Peroxidase (HRP) is added  to  each  microplate  well  and incubated. Then a TMB substrate solution is added to each well. Only those wells that contain SOCS5, biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of a sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450 nm ± 2 nm. The concentration of SOCS5 in the samples is then determined by comparing the O.D. of the samples to the standard curve.

 

Sample collection and storage 

Serum - Use a serum separator tube (SST) and allow samples to clot for 30 minutes before centrifugation for 15 minutes at approximately 1000 × g. Remove serum and assay immediately or aliquot and store samples at -20

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