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Human CD95 / FAS Recombinant (Human IgG1 Fc) Protein LS-G3926

Ordering

Wt. Vol. Conc. Price
50 µg - - $365
Inquire for larger quantities
LSBio (Direct) LSBio (Direct)
206-374-1102
866-206-6909
Orders@LSBio.com
 

Most Popular CD95 / FAS Proteins

Human CD95 / FAS Recombinant Protein - LS-G16686
E. coli Expression System
None
Unpurified
Human CD95 / FAS Recombinant Protein - LS-G19993
E. coli Expression System
None
Unpurified / Lyophilized
Mouse CD95 / FAS Recombinant (6His,C-terminus) Protein - LS-G40287
Human Human Cells
6His,C-terminus
Unpurified

100% Guaranteed 100% Guaranteed
LS-G3926
Recombinant Protein
CD95 / FAS
Human
~47kDa (SDS-PAGE)
The Fc portion of human IgG1 is fused to the C-terminus of human Fas (aa 26-170).
aa 26-170
HEK 293 Cells
Human
Human IgG1 Fc
Greater than 95% by SDS-PAGE
Blocks the binding of FasL to Fas.
Less than 0.01 EU/µg protein (determined by LAL method).
Lyophilized from PBS.
Reconstitute with 50 µl sterile water.
Store lyophilized at -20°C for at least 6 months. Once reconstituted store at +4°C for immediate use.
For research use only.

About CD95 / FAS

P25445 NM_152877 NP_000034.1

FAS Protein, ALPS1A Protein, APO-1 Protein, APT1 Protein, Apo-1 antigen Protein, APO-1 cell surface antigen Protein, Apo11 antigen Protein, Apoptosis antigen 1 Protein, CD95 antigen Protein, Delta Fas/APO-1/CD95 Protein, Fas AMA Protein, FAS1 Protein, Fasl receptors Protein, FASLG receptor Protein, FASTM Protein, FAS 827dupA Protein, Fasl receptor Protein, TNFRSF6 Protein, CD95 Protein

CD95 / FAS is a member of the TNF-receptor superfamily. This receptor contains a death domain. It has been shown to play a central role in the physiological regulation of programmed cell death, and has been implicated in the pathogenesis of various malignancies and diseases of the immune system. The interaction of this receptor with its ligand allows the formation of a death-inducing signaling complex that includes Fas-associated death domain protein (FADD), caspase 8, and caspase 10.

Requested From: United States
Date Requested: 12/2/2016

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