G6PC anticorps (AA 123-149)

N° du produit ABIN651417

Détail du produit anti-G6PC anticorps

Antigène: G6PC (Glucose 6-Phosphatase, Catalytic (G6PC))

Épitope: AA 123-149

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp G6PC 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 G6PC antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 123-149 amino acids from the Central region of human G6PC.

Clone: RB30027

Isotype: Ig Fraction

Information d'application

Indications d'application: WB: 1:1000. WB: 1:1000. IHC-P: 1:50~100. 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: 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.

Date de péremption: 6 months

Détails sur G6PC

Antigène: G6PC (Glucose 6-Phosphatase, Catalytic (G6PC))

Autre désignation: G6PC (G6PC Produits)

Synonymes: anticorps AW107337, anticorps G6Pase, anticorps G6pt, anticorps Glc-6-Pase, anticorps G6PC1, anticorps G6PT, anticorps GSD1, anticorps GSD1a, anticorps G-6-Pase, anticorps glucose-6-phosphatase, catalytic, anticorps glucose-6-phosphatase catalytic subunit, anticorps glucose-6-phosphatase, catalytic subunit, anticorps G6pc, anticorps G6PC

Sujet: Glucose-6-phosphatase is an integral membrane protein of the endoplasmic reticulum that catalyzes the hydrolysis of D-glucose 6-phosphate to D-glucose and orthophosphate. It is a key enzyme in glucose homeostasis, functioning in gluconeogenesis and glycogenolysis. Defects in the enzyme cause glycogen storage disease type I.

Poids moléculaire: 40484

ID gène: 2538

NCBI Accession: NP_000142, NP_001257326

UniProt: P35575

Pathways: Carbohydrate Homeostasis, Cellular Glucan Metabolic Process