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AMPD1 antibody
AMPD1
Reactivity: Human
ELISA, WB, IHC
Host: Rabbit
Polyclonal
unconjugated
Product Details anti-AMPD1 Antibody
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Target
See all AMPD1 Antibodies
AMPD1
(Adenosine Monophosphate Deaminase 1 (AMPD1))
Reactivity
All reactivities for AMPD1 antibodies
Human
Host
All hosts for AMPD1 antibodies
Rabbit
Clonality
All clonalities for AMPD1 antibodies
Polyclonal
Conjugate
All conjugates for AMPD1 antibodies
This AMPD1 antibody is un-conjugated
Application
All applications for AMPD1 antibodies
ELISA, Western Blotting (WB), Immunohistochemistry (IHC)
Characteristics
Polyclonal Antibody
Purification
Affinity purification
Immunogen
Synthetic peptide of human AMPD1
Isotype
IgG
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Alternatives
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Application Details
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Application Notes
WB 1:1000-1:5000, IHC 1:100-1:300
Restrictions
For Research Use only
Handling
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Format
Liquid
Concentration
1 mg/mL
Buffer
PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4
Preservative
Sodium azide
Precaution of Use
This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
Storage
-20 °C
Storage Comment
Store at -20°C. Avoid freeze / thaw cycles.
Target Details for AMPD1
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Target
AMPD1
(Adenosine Monophosphate Deaminase 1 (AMPD1))
Alternative Name
AMPD1 (AMPD1 Products )
Synonyms
ampd1 antibody, MAD antibody, MADA antibody, AI553520 antibody, Ampd-1 antibody, Ampd01 antibody, RATAMPD01 antibody, zgc:77905 antibody, adenosine monophosphate deaminase 1 antibody, N-acetyl-anhydromuranmyl-L-alanine amidase antibody, N-acetylmuramoyl-L-alanine amidase antibody, Negative regulator of beta-lactamase expression antibody, adenosine monophosphate deaminase 1 (isoform M) antibody, AMPD1 antibody, ampD1 antibody, ampd1 antibody, Ampd1 antibody
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.
Molecular Weight
90 kDa
NCBI Accession
NP_000027
UniProt
P23109
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