POMT1 anticorps (C-Term)

N° du produit ABIN5537760

Détail du produit anti-POMT1 anticorps

Antigène: POMT1 (Protein-O-Mannosyltransferase 1 (POMT1))

Épitope: AA 706-735, C-Term

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp POMT1 est non-conjugé

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

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

Immunogène: This POMT1 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 706-735 amino acids from the C-terminal region of human POMT1.

Isotype: Ig Fraction

Information d'application

Indications d'application: For IHC-P starting dilution is: 1:10~50

For WB starting dilution is: 1:1000

For FACS starting dilution is: 1:10~50

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 0.29 mg/mL

Buffer: Supplied in PBS with 0.09 % (W/V) sodium azide.

Agent conservateur: Sodium azide

Précaution d'utilisation: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Stock: 4 °C,-20 °C

Stockage commentaire: Store at 4°C for three months and -20°C, stable for up to one year. As with all antibodies care should be taken to avoid repeated freeze thaw cycles. Antibodies should not be exposed to prolonged high temperatures.

Détails sur POMT1

Antigène: POMT1 (Protein-O-Mannosyltransferase 1 (POMT1))

Autre désignation: POMT1 (POMT1 Produits)

Synonymes: anticorps LGMD2K, anticorps MDDGA1, anticorps MDDGB1, anticorps MDDGC1, anticorps RT, anticorps AI505244, anticorps protein O-mannosyltransferase 1, anticorps protein-O-mannosyltransferase 1, anticorps POMT1, anticorps Pomt1

Sujet: The protein encoded by this gene is an O-mannosyltransferase that requires interaction with the product of the POMT2 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) and limb-girdle muscular dystrophy type 2K (LGMD2K). Several transcript variants encoding different isoforms have been found for this gene.

Poids moléculaire: 85 kDa

ID gène: 10585

UniProt: Q9Y6A1