AMPD3 monoclonal antibody, clone AMPD3/901
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More Files
- More Functions
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)
Immunohistochemical staining (Formalin-fixed paraffin-embedded sections) of human tonsil (A) and human placenta (B) with AMPD3 monoclonal antibody, clone AMPD3/901 (Cat # MAB13287).
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Specification
Product Description
Mouse monoclonal antibody raised against full length recombinant human AMPD3.
Immunogen
Recombinant protein corresponding to full length human AMPD3.
Host
Mouse
Theoretical MW (kDa)
~90
Reactivity
Human
Form
Liquid
Purification
Protein A/G purification
Isotype
IgG2b, kappa
Recommend Usage
Flow Cytometry (1-2 ug/106 cells in 0.1 mL)
Immunocytochemistry (1-2 ug/mL)
Immunofluorescence (0.5-1 ug/mL)
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) (2-4 ug/mL)
The optimal working dilution should be determined by the end user.Storage Buffer
In 10 mM PBS (0.05% BSA, 0.05% sodium azide).
Storage Instruction
Store at 4°C.
Note
This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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Applications
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)
Immunohistochemical staining (Formalin-fixed paraffin-embedded sections) of human tonsil (A) and human placenta (B) with AMPD3 monoclonal antibody, clone AMPD3/901 (Cat # MAB13287).Immunocytochemistry
Immunofluorescence
Flow Cytometry
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Gene Info — AMPD3
Entrez GeneID
272Protein Accession#
Q01432Gene Name
AMPD3
Gene Alias
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Gene Description
adenosine monophosphate deaminase (isoform E)
Omim ID
102772Gene Ontology
HyperlinkGene Summary
This gene encodes a member of the AMP deaminase gene family. The encoded 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. This gene encodes the erythrocyte (E) isoforms, whereas other family members encode isoforms that predominate in muscle (M) and liver (L) cells. Mutations in this gene lead to the clinically asymptomatic, autosomal recessive condition erythrocyte AMP deaminase deficiency. Alternatively spliced transcript variants encoding different isoforms of this gene have been described. [provided by RefSeq
Other Designations
AMP aminohydrolase|AMP deaminase 3|adenosine monophosphate deaminase 3|erythrocyte type AMP deaminase|erythrocyte-specific AMP deaminase|myoadenylate deaminase
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Interactome
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Pathway
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Disease
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