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Mouse FAS/CD95 (Factor Related Apoptosis) ELISA Kit

Product Specifications

CAS Number

7732-18-5

Abbreviation

FAS;CD95

Synonyms

FASR; TNFRSF6; APO1; APT1; FAS1; FASTM; ALPS1A;

UniProt

P25446

Species Reactivity

Mouse

Cross Reactivity

This kit recognizes Mouse FAS/CD95 in samples.No significant cross-reactivity or interference between Mouse FAS/CD95 and analogues was observed

Target

Mouse

Type

Sandwich-ELISA

Applications

ELISA

Field of Research

Cancer; Cell Biology; Immunology

Detection Method

Colormetric

Assay Principle

This ELISA kit uses the Sandwich-ELISA principle. The micro ELISA plate provided in this kit has been pre-coated with an antibody specific to Mouse FAS/CD95. Standards or samples are added to the micro ELISA plate wells and combined with the specific antibody. Then a biotinylated detection antibody specific for Mouse FAS/CD95 and Avidin-Horseradish Peroxidase (HRP) conjugate are added successively to each micro plate well and incubated. Free components are washed away. The substrate solution is added to each well. Only those wells that contain Mouse FAS/CD95, biotinylated detection antibody and Avidin-HRP conjugate will appear blue in color. The enzyme-substrate reaction is terminated by the addition of stop solution and the color turns yellow. The optical density (OD) is measured spectrophotometrically at a wavelength of 450 nm ± 2 nm. The OD value is proportional to the concentration of Mouse FAS/CD95. You can calculate the concentration of Mouse FAS/CD95 in the samples by comparing the OD of the samples to the standard curve.

Assay Performance Time

3 h 30 min

Sample Type

Serum, plasma and other biological fluids

Detection Range

0.16-10 ng/mL

Precision

Both intra-CV and inter-CV are < 10%

Recovery

80%-120%

Sensitivity

0.1 ng/mL

Shipping Conditions

Ice bag

Storage Conditions

2-8°C/-20°C,12 months

Applications Notes

This ELISA kit applies to the in vitro quantitative determination of Mouse FAS/CD95 concentrations in serum, plasma and other biological fluids.

Citation 01

https://link.springer.com/article/10.1007/s00210-018-1579-0

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