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AMPD1 anticorps
AMPD1
Reactivité: Humain
ELISA, WB, IHC
Hôte: Lapin
Polyclonal
unconjugated
N° du produit ABIN2432475
Détail du produit anti-AMPD1 anticorps
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Antigène
Voir toutes AMPD1 Anticorps
AMPD1
(Adenosine Monophosphate Deaminase 1 (AMPD1))
Reactivité
Toutes les réactivités sur AMPD1 Anticorps
Humain
Hôte
Toutes les hôtes sur AMPD1 Anticorps
Lapin
Clonalité
Toutes les clonalités sur AMPD1 Anticorps
Polyclonal
Conjugué
Tous les conjugués à travers AMPD1 Anticorps
Cet anticorp AMPD1 est non-conjugé
Application
Tous les applications à travers AMPD1 Anticorps.
ELISA, Western Blotting (WB), Immunohistochemistry (IHC)
Purification
Affinity purification
Immunogène
Synthetic peptide of human AMPD1
Isotype
IgG
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Alternatives
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Information d'application
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Indications d'application
WB 1:500-1:2000, IHC 1:100-1:300
Restrictions
For Research Use only
Stockage
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Format
Liquid
Concentration
0.5 mg/mL
Buffer
PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4
Agent conservateur
Sodium azide
Conseil sur la manipulation
Avoid freeze / thaw cycles.
Stock
-20 °C
Stockage commentaire
Store at -20°C. Avoid freeze / thaw cycles.
Détails sur AMPD1
(cache)
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.
Poids moléculaire
Calculated MW: 90 kDa
NCBI Accession
NP_000027
Vus récemment
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