PIGP antibody (N-Term)

Catalog No. ABIN1538804

The Rabbit Polyclonal anti-PIGP antibody has been validated for WB. It is suitable to detect PIGP in samples from Human.

Quick Overview for PIGP antibody (N-Term) (ABIN1538804)

Target: PIGP (Phosphatidylinositol Glycan Anchor Biosynthesis, Class P (PIGP))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This PIGP antibody is un-conjugated

Application: Western Blotting (WB)

Clone: RB36402

Product Details anti-PIGP Antibody

Binding Specificity: AA 2-30, N-Term

Purification: This antibody is purified through a protein A column, followed by peptide affinity purification.

Immunogen: This PIGP antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 2-30 amino acids from the N-terminal region of human PIGP.

Isotype: Ig Fraction

Application Details

Application Notes: WB: 1:1000

Restrictions: For Research Use only

Handling

Format: Liquid

Buffer: Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) 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: 4 °C,-20 °C

Storage Comment: PIGP Antibody (N-term) can be refrigerated at 2-8 °C for up to 6 months. For long term storage, keep at -20 °C.

Expiry Date: 6 months

Target Details for PIGP

Target: PIGP (Phosphatidylinositol Glycan Anchor Biosynthesis, Class P (PIGP))

Alternative Name: PIGP

Background: This gene encodes an enzyme involved in the first step of glycosylphosphatidylinositol (GPI)-anchor biosynthesis. The GPI-anchor is a glycolipid found on many blood cells that serves to anchor proteins to the cell surface. The encoded protein is a component of the GPI-N-acetylglucosaminyltransferase complex that catalyzes the transfer of N-acetylglucosamine (GlcNAc) from UDP-GlcNAc to phosphatidylinositol (PI). This gene is located in the Down Syndrome critical region on chromosome 21 and is a candidate for the pathogenesis of Down syndrome. Alternatively spliced transcript variants encoding different isoforms have been described.

Molecular Weight: 18089

Gene ID: 51227

NCBI Accession: NP_710148, NP_710149

UniProt: P57054

Pathways: Inositol Metabolic Process