AMPD3 anticorps (AA 325-356)

N° du produit ABIN1538324

Détail du produit anti-AMPD3 anticorps

Antigène: AMPD3 (Adenosine Monophosphate Deaminase 3 (AMPD3))

Épitope: AA 325-356

Reactivité: Humain, Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp AMPD3 est non-conjugé

Application: Western Blotting (WB)

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

Immunogène: This AMPD3 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 325-356 amino acids from the Central region of human AMPD3.

Clone: RB17671

Isotype: Ig Fraction

Information d'application

Indications d'application: WB: 1:1000. 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 deg C for up to 6 months. For long term storage store at -20 deg C in small aliquots to prevent freeze-thaw cycles.

Date de péremption: 6 months

Détails sur AMPD3

Antigène: AMPD3 (Adenosine Monophosphate Deaminase 3 (AMPD3))

Autre désignation: AMPD3 (AMPD3 Produits)

Synonymes: anticorps ampd3, anticorps fi25h10, anticorps wu:fi25h10, anticorps zgc:55390, anticorps MGC108215, anticorps adenosine monophosphate deaminase 3, anticorps adenosine monophosphate deaminase 3b, anticorps AMP deaminase 3, anticorps AMPD3, anticorps ampd3b, anticorps PTRG_08116, anticorps ampd3, anticorps Ampd3

Sujet: AMPD3 is a member of the AMP deaminase gene family. This protein is a highly regulated enzyme that catalyzes the hydrolytic deamination of adenosine monophosphate to inosine monophosphate, a branch point in the adenylate catabolic pathway. The protein is the erythrocyte (E) isoforms, whereas other family members isoforms predominate in muscle (M) and liver (L) cells. Mutations in this gene lead to the clinically asymptomatic, autosomal recessive condition erythrocyte AMP deaminase deficiency.

Poids moléculaire: 88812

ID gène: 272

NCBI Accession: NP_000471, NP_001020560, NP_001020561, NP_001165901, NP_001165902

UniProt: Q01432