AMPD1 Polyclonal Antibody
For reference only. Please follow the manual included in your kit for instructions.
Catalog Number
RD76632A
Western Blot analysis of Human fetal muscle tissue, K562 and hela cell using AMPD1 Polyclonal Antibody at dilution of 1:1600
Immunohistochemistry of paraffin-embedded Human liver cancer using AMPD1 Polyclonal Antibody at dilution of 1:80
Immunohistochemistry of paraffin-embedded Human lung cancer using AMPD1 Polyclonal Antibody at dilution of 1:80
Variation
Quantity
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Overview
Product Name
AMPD1 Polyclonal Antibody
Catalog Number
RD76632A
Clonality
Polyclonal
Purification Method
Affinity purification
Isotype
IgG
Host
Rabbit
Background
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.
Immunogen Information
Immunogen
Synthetic peptide of human AMPD1
Swissprot
P23109
Synonyms
Adenosine monophosphate deaminase 1 (isoform M)Adenosine monophosphate deaminase 1AMP deaminase 1AMP deaminase isoform MAMPD 1AMPDAmpd01MADMADAMyoadenylate deaminaseRATAMPD01Skeletal muscle AMPD
Calculated MW
90 kDa
Gene Accession
NP_000027
Applications
Reactivity
Human
Tested Applications
WB,IHC,ELISA
Conjugation
Unconjugated
Dilution
WB 1:1000-1:5000, IHC 1:100-1:300
Concentration
1 mg/mL
Storage Buffer
PBS with 0.05% sodium azide and 50% glycerol, PH7.4
Storage Instructions
Store at -20°C. Avoid freeze / thaw cycles.
Research Areas