AMPD1 anticorps (AA 50-260)

N° du produit ABIN1678653

Détail du produit anti-AMPD1 anticorps

Antigène: AMPD1 (Adenosine Monophosphate Deaminase 1 (AMPD1))

Épitope: AA 50-260

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp AMPD1 est non-conjugé

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

Séquence: AEKVFASEVK DEGGRQEISP FDVDEICPIS HHEMQAHIFH LETLSTSTEA RRKKRFQGRK TVNLSIPLSE TSSTKLSHID EYISSSPTYQ TVPDFQRVQI TGDYASGVTV EDFEIVCKGL YRALCIREKY MQKSFQRFPK TPSKYLRNID GEAWVANESF YPVFTPPVKK GEDPFRTDNL PENLGYHLKM KDGVVYVYPN EAAVSKDEPK P

Réactivité croisée: Humain, Souris, Rat

Attributs du produit: Polyclonal Antibodies

Purification: Affinity purification

Immunogène: Recombinant fusion protein containing a sequence corresponding to amino acids 50-260 of human AMPD1 (NP_001166097.1).

Isotype: IgG

Information d'application

Indications d'application: WB,1:500 - 1:2000,IF,1:50 - 1:200

Restrictions: For Research Use only

Stockage

Buffer: PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.

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: -20 °C

Stockage commentaire: Store at -20°C. Avoid freeze / thaw cycles.

Détails sur AMPD1

Antigène: AMPD1 (Adenosine Monophosphate Deaminase 1 (AMPD1))

Autre désignation: AMPD1 (AMPD1 Produits)

Synonymes: anticorps ampd1, anticorps MAD, anticorps MADA, anticorps AI553520, anticorps Ampd-1, anticorps Ampd01, anticorps RATAMPD01, anticorps zgc:77905, anticorps adenosine monophosphate deaminase 1, anticorps N-acetyl-anhydromuranmyl-L-alanine amidase, anticorps N-acetylmuramoyl-L-alanine amidase, anticorps Negative regulator of beta-lactamase expression, anticorps adenosine monophosphate deaminase 1 (isoform M), anticorps AMPD1, anticorps ampD1, anticorps ampd1, anticorps Ampd1

Sujet: Adenosine monophosphate deaminase 1 catalyzes the deamination of AMP to IMP in skeletal muscle and plays an important role in the purine nucleotide cycle. Two other genes have been identified, AMPD2 and AMPD3, for the liver- and erythocyte-specific isoforms, respectively. Deficiency of the muscle-specific enzyme is apparently a common cause of exercise-induced myopathy and probably the most common cause of metabolic myopathy in the human. Alternatively spliced transcript variants encoding different isoforms have been identified in this gene.,AMPD1,MAD,MADA,MMDD,Cancer,Signal Transduction,Endocrine & Metabolism,AMPD1

Poids moléculaire: 89 kDa/90 kDa

ID gène: 270

UniProt: P23109