GBE1 anticorps (AA 527-556)

N° du produit ABIN653459

L’anticorps Lapin Polyclonal anti-GBE1 a été validé pour WB et IF. Il convient pour détecter GBE1 dans des échantillons de Humain et Souris.

Aperçu rapide pour GBE1 anticorps (AA 527-556) (ABIN653459)

Antigène: GBE1 (Glucan (1,4-alpha-), Branching Enzyme 1 (GBE1))

Reactivité: Humain, Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp GBE1 est non-conjugé

Application: Western Blotting (WB), Immunofluorescence (IF)

Clone: RB24029

Détail du produit anti-GBE1 anticorps

Épitope: AA 527-556

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

Immunogène: This GBE1 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 527-556 amino acids from the Central region of human GBE1.

Isotype: Ig Fraction

Information d'application

Indications d'application: IF: 1:10~50. WB: 1:1000. WB: 1:1000

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 GBE1

Antigène: GBE1 (Glucan (1,4-alpha-), Branching Enzyme 1 (GBE1))

Autre désignation: GBE1

Sujet: GBE1 is a glycogen branching enzyme that catalyzes the transfer of alpha-1,4-linked glucosyl units from the outer end of a glycogen chain to an alpha-1,6 position on the same or a neighboring glycogen chain. Branching of the chains is essential to increase the solubility of the glycogen molecule and, consequently, in reducing the osmotic pressure within cells. Highest level of this enzyme are found in liver and muscle. Mutations in this gene are associated with glycogen storage disease IV (also known as Andersen's disease).

Poids moléculaire: 80474

ID gène: 2632

NCBI Accession: NP_000149

UniProt: Q04446

Pathways: Cellular Glucan Metabolic Process