PEMT antibody (C-Term)

Catalog No. ABIN387868

Product Details anti-PEMT Antibody

Target: PEMT (Phosphatidylethanolamine N-Methyltransferase (PEMT))

Binding Specificity: AA 170-199, C-Term

Reactivity: Human, Mouse

Host: Rabbit

Clonality: Polyclonal

Conjugate: This PEMT antibody is un-conjugated

Application: Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

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

Immunogen: This PEMT antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 170-199 amino acids from the C-terminal region of human PEMT.

Clone: RB12628

Isotype: Ig Fraction

Application Details

Application Notes: WB: 1:1000. IHC-P: 1:100. IHC-P: 1:100

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: Maintain refrigerated at 2-8 °C for up to 6 months. For long term storage store at -20 °C in small aliquots to prevent freeze-thaw cycles.

Expiry Date: 6 months

Target Details for PEMT

Target: PEMT (Phosphatidylethanolamine N-Methyltransferase (PEMT))

Alternative Name: PEMT (PEMT Products)

Synonyms: zgc:55479 antibody, DDBDRAFT_0204815 antibody, DDBDRAFT_0267053 antibody, DDB_0204815 antibody, DDB_0267053 antibody, DDBDRAFT_0219474 antibody, DDBDRAFT_0267052 antibody, DDB_0219474 antibody, DDB_0267052 antibody, PEAMT antibody, PEMPT antibody, PEMT2 antibody, PNMT antibody, AI255394 antibody, Pempt antibody, Pempt2 antibody, PHOMETH antibody, phosphatidylethanolamine N-methyltransferase antibody, pemt antibody, MCA3065 antibody, pmtA antibody, CNG04250 antibody, pemtA antibody, pemtB antibody, PEMT antibody, Pemt antibody

Background: PEMT is an enzyme which converts phosphatidylethanolamine to phosphatidylcholine by sequential methylation in the liver. The protein localizes to the endoplasmic reticulum and mitochondria-associated membranes. The gene is within the Smith-Magenis syndrome region on chromosome 17.

Molecular Weight: 22134

Gene ID: 10400

NCBI Accession: NP_001254480, NP_001254481, NP_009100, NP_680477, NP_680478

UniProt: Q9UBM1