POMT2 antibody (N-Term) (PE)

Catalog No. ABIN8028601

The PE-conjugated Rabbit Polyclonal anti-POMT2 antibody (ABIN8028601) specifically detects POMT2 in FACS. The antibody is reactive with Human, Mouse and Rat samples.

Quick Overview for POMT2 antibody (N-Term) (PE) (ABIN8028601)

Target: POMT2 (Protein-O-Mannosyltransferase 2 (POMT2))

Reactivity: Human, Mouse, Rat

Host: Rabbit

Clonality: Polyclonal

Conjugate: This POMT2 antibody is conjugated to PE

Application: Flow Cytometry (FACS)

Product Details anti-POMT2 Antibody (PE)

Binding Specificity: N-Term

Purpose: Anti-POMT2 Antibody PE Conjugated

Specificity: No cross reactivity with other proteins.

Cross-Reactivity (Details): No cross-reactivity with other proteins.

Purification: Immunogen affinity purified.

Immunogen: A synthetic peptide corresponding to a sequence at the N-terminus of human POMT2, which shares 61.9% amino acid (aa) sequence identity with both mouse and rat POMT2.

Isotype: IgG

Application Details

Application Notes: Flow Cytometry, Optimal dilutions should be determined by end users.

Restrictions: For Research Use only

Handling

Format: Liquid

Buffer: Each vial contains 50 % glycerol, 0.9 % NaCl, 0.2 % Na2HPO4, 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: At -20°C for one year from date of receipt. Avoid repeated freezing and thawing. Protect from light.

Expiry Date: 12 months

Target Details for POMT2

Target: POMT2 (Protein-O-Mannosyltransferase 2 (POMT2))

Alternative Name: POMT2

Background:

Background: Protein O-mannosyl-transferase 2 is an enzyme that in humans is encoded by the POMT2 gene. This gene is mapped to chromosome 14q24.3. The protein encoded by this gene is an O-mannosyltransferase that requires interaction with the product of the POMT1 gene for enzymatic function. The encoded protein is found in the membrane of the endoplasmic reticulum. Defects in this gene are a cause of Walker-Warburg syndrome (WWS).

Gene Full Name: protein O-mannosyltransferase 2

Gene ID: 29954

UniProt: Q9UKY4