Intrinsic Factor anticorps (AA 189-218)

N° du produit ABIN656899

Cet anticorps Lapin Polyclonal détecte spécifiquement Intrinsic Factor dans WB, IF, FACS et IHC (p). Il présente une réactivité envers Humain.

Aperçu rapide pour Intrinsic Factor anticorps (AA 189-218) (ABIN656899)

Antigène: Intrinsic Factor (GIF) (Gastric Intrinsic Factor (Vitamin B Synthesis) (GIF))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp Intrinsic Factor est non-conjugé

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

Clone: RB32460

Détail du produit anti-Intrinsic Factor anticorps

Épitope: AA 189-218

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

Immunogène: This GIF antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 189-218 amino acids from the Central region of human GIF.

Isotype: Ig Fraction

Information d'application

Indications d'application: IF: 1:10~50. WB: 1:1000. IHC-P: 1:10~50. FC: 1:10~50

Restrictions: For Research Use only

Stockage

Format: Liquid

Buffer: Purified polyclonal antibody 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: GIF Antibody (Center) can be refrigerated at 2-8 °C for up to 6 months. For long term storage, place the at -20 °C.

Date de péremption: 6 months

Détails sur Intrinsic Factor

Antigène: Intrinsic Factor (GIF) (Gastric Intrinsic Factor (Vitamin B Synthesis) (GIF))

Autre désignation: GIF

Sujet: This gene is a member of the cobalamin transport protein family. It encodes a glycoprotein secreted by parietal cells of the gastric mucosa and is required for adequate absorption of vitamin B12. Vitamin B12 is necessary for erythrocyte maturation and mutations in this gene may lead to congenital pernicious anemia.

Poids moléculaire: 45416

ID gène: 2694

NCBI Accession: NP_005133

UniProt: P27352