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Rabbit Anti-Swine Fas Ligand Polyclonal Antibody

Cat. No.VD10H60

Product TypeAnimal-targeted Antibodies

Size

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Product Overview

O16H60 polyclonal antibody is specific for Swine Fas ligand (FasL), also known as CD95L and CD178. It was purified from whole serum by affinity chromatography. It can be applied for ELISA and Western Blot (WB).

Specifications

Application ELISA; WB

Clonality Polyclonal Antibody

Classification Primary Antibody

Clone O16H60

Host Rabbit

Target Species Swine

Species Reactivity Swine

Specificity Swine Fas Ligand

Immunogen Recombinant Swine FasL

Purification Affinity chromatography Purified

Purity ≥ 90% (SDS-PAGE)

Concentration 1.0 mg/mL

Conjugation Unconjugated

Preservative and Stabilizer 0.09% Sodium azide (NaN₃)

Buffer Phosphate buffered saline

Physical State Liquid

Target Information

Fas ligand (FasL), also known as CD95L or CD178 is a type-II transmembrane protein expressed on cytotoxic T lymphocytes and natural killer (NK) cells. Its binding with Fas receptor (FasR) induces programmed cell death in the FasR-carrying target cell. Swine FasL overexpression in endothelial cells (EC) of vascularized xenografts may provide protection from cellular xenograft rejection. Fas ligand/receptor interactions play an important role in the regulation of the immune system and the progression of cancer.

Target Swine Fas Ligand

Target Synonym FASLG; ALPS1B; APT1LG1; APTL; CD178; CD95-L; CD95L; FASL; TNFSF6; TNLG1A

Gene ID 396726

UniProt ID Q9BEA8

Shipping and Storage

This product is shipped at ambient temperature. It is recommended to aliquot and store at 2-8°C on receipt.

Documents

Datasheet

COA

To request a Certificate of Analysis, please enter the Lot No. in the search box. Note: Certificate of Analysis not available for kits.

The product is for research use only.
Not for commercial, prophylactic, diagnostic, or therapeutic applications.

References

Seol, Jae Goo, et al. "Production of transgenic cloned miniature pigs with membrane-bound human fas ligand (FasL) by somatic cell nuclear transfer." Nature Precedings (2010): 1-1.