DPM1 antibody

Catalog No. ABIN7263775

Product Details anti-DPM1 Antibody

Target: DPM1 (Dolichyl-Phosphate Mannosyltransferase Polypeptide 1, Catalytic Subunit (DPM1))

Reactivity: Human, Mouse, Rat

Host: Rabbit

Clonality: Polyclonal

Conjugate: This DPM1 antibody is un-conjugated

Application: Immunofluorescence (IF)

Characteristics: Polyclonal Antibody

Purification: Affinity purification

Immunogen: Recombinant fusion protein of human DPM1 (NP_003850.1).

Isotype: IgG

Application Details

Application Notes: IF 1:50-1:200

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 1 mg/mL

Buffer: PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3

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. Avoid freeze / thaw cycles.

Target Details for DPM1

Target: DPM1 (Dolichyl-Phosphate Mannosyltransferase Polypeptide 1, Catalytic Subunit (DPM1))

Alternative Name: DPM1 (DPM1 Products)

Synonyms: DPM1 antibody, zgc:101018 antibody, MGC114892 antibody, AI118379 antibody, AI194292 antibody, CDGIE antibody, MPDS antibody, DPMS antibody, dolichyl-phosphate mannosyltransferase polypeptide 1, catalytic subunit antibody, dolichyl-phosphate mannosyltransferase subunit 1, catalytic antibody, dolichyl-phosphate mannosyltransferase polypeptide 1, catalytic subunit S homeolog antibody, dolichol-phosphate (beta-D) mannosyltransferase 1 antibody, dpm1 antibody, DPM1 antibody, dpm1.S antibody, Dpm1 antibody

Background: Dolichol-phosphate mannose (Dol-P-Man) serves as a donor of mannosyl residues on the lumenal side of the endoplasmic reticulum (ER). Lack of Dol-P-Man results in defective surface expression of GPI-anchored proteins. Dol-P-Man is synthesized from GDP-mannose and dolichol-phosphate on the cytosolic side of the ER by the enzyme dolichyl-phosphate mannosyltransferase. Human DPM1 lacks a carboxy-terminal transmembrane domain and signal sequence and is regulated by DPM2. Mutations in this gene are associated with congenital disorder of glycosylation type Ie. Alternative splicing results in multiple transcript variants.

Gene ID: 8813

UniProt: O60762

Pathways: Inositol Metabolic Process