TPGS2 antibody

Catalog No. ABIN8120562

The Rabbit Polyclonal anti-TPGS2 antibody is suitable to detect TPGS2 in samples from Human, Mouse and Rat. It has been validated for WB and ELISA.

Quick Overview for TPGS2 antibody (ABIN8120562)

Target: TPGS2 (C18orf10) (Chromosome 18 Open Reading Frame 10 (C18orf10))

Reactivity: Human, Mouse, Rat

Host: Rabbit

Clonality: Polyclonal

Conjugate: This TPGS2 antibody is un-conjugated

Application: Western Blotting (WB), ELISA

Product Details anti-TPGS2 Antibody

Purpose: PGS2 Antibody

Specificity: PGS2 Polyclonal Antibody detects endogenous levels of protein.

Purification: The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

Immunogen: Synthesized peptide derived from part region of human protein

Isotype: IgG

Application Details

Application Notes: WB 1:500-2000 ELISA 1:5000-20000

Restrictions: For Research Use only

Handling

Format: Liquid

Buffer: Liquid in PBS containing 50 % glycerol, and 0.02 % sodium azide.

Preservative: Sodium azide

Precaution of Use: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Storage: -20 °C

Storage Comment: Store at -20°C/1 year

Expiry Date: 12 months

Target Details for TPGS2

Target: TPGS2 (C18orf10) (Chromosome 18 Open Reading Frame 10 (C18orf10))

Alternative Name: PGS2

Background:

Background: This gene encodes a member of the small leucine-rich proteoglycan family of proteins. Alternative splicing results in multiple transcript variants, at least one of which encodes a preproprotein that is proteolytically processed to generate the mature protein. This protein plays a role in collagen fibril assembly. Binding of this protein to multiple cell surface receptors mediates its role in tumor suppression, including a stimulatory effect on autophagy and inflammation and an inhibitory effect on angiogenesis and tumorigenesis. This gene and the related gene biglycan are thought to be the result of a gene duplication. Mutations in this gene are associated with congenital stromal corneal dystrophy in human patients. [provided by RefSeq, Nov 2015],

Gene Name: DCN SLRR1B

Protein Name: Decorin (Bone proteoglycan II) (PG-S2) (PG40)

Gene ID: 1634

UniProt: P07585