Human sFAS ELISA Kit View larger

Human sFAS ELISA Kit

FM-E100019

$599.00

Data sheet

Product Citations "Evaluation of Serum Perforin, Caspase-3, sFasL and M-30 Levels as Apoptotic Markers in Children With Crimean-Congo Hemorrhagic Fever, Güven, Ahmet S. et al, The Pediatric Infectious Disease Journal: February 2015 - Volume 34 - Issue 2 - p 208–213 doi: 10.1097/INF.0000000000000530"

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Assay Range

31.2-2,000 pg/mL  

Sensitivity

3.0 pg/mL

Size

96T

Storage

Store at 2 - 8ºC. Keep reconstituted standard and detection Ab at -20 ºC

Assay Principle

Sandwich ELISA

Sample Volume

100 µL final volume, dilution factor varies on samples

Detection Method

Chromogenic

 

 

Kit Components

 

 1. Recombinant Human sFAS standard: 2 vials

 2. One 96-well plate coated with Human sFAS  Ab

 3. Sample diluent buffer: 12 mL - 1

 4. Detection antibody: 130 µL, dilution 1:100

 5. Streptavidin-HRP: 130 µL, dilution 1:100

 6. Antibody diluent buffer: 12 mL x1   

 7. Streptavidin-HRP diluent buffer: 12 mL x1

 8. TMB developing agent: 10 mL x1

 9. Stop solution: 10 mL x1

10. Washing solution (20x): 25 mL x1

 

 

Background

 

Fas, also known as FAS receptor (FasR), apoptosis antigen 1 (APO-1 or APT), cluster of CD95 or tumor necrosis factor receptor superfamily member 6 (TNFRSF6), is a glycoprotein belonging to the Tumor Necrosis Factor Receptor Superfamily (TNFRSF). Fas is mainly expressed on activated T and B lymphocytes, and on malignant lymphoid cells. Fas is also expressed on cells from liver, heart, kidney, ovaries, and on many other malignant cells. Fas ligand (FasL), the physiological agonist for Fas, is also a transmembrane protein with homology to the TNF family in its extracellular domain. FasL is expressed primarily by activated T lymphocytes and by cells of the small intestine and lung. Five soluble Fas (sFas) proteins derived from alternatively spliced transcrpts of Fas gene have been detected in the supernatant of cultures of peripheral blood mononuclear cells or certain tumor cell lines. Interaction of FasL with Fas plays a very important role in initiating apoptotic signaling pathways. Mutations in Fas gene have been detected in humans with autoimmune lymphoproliferative syndrome. Mice with mutations in either Fas or FasL exhibit accumulation of activated lymphocytes and classical autoimmune symptoms, suggesting that Fas-mediated apoptosis might primarily eliminate activated immune cells from the peripheral circulation.

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