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AMPD3 encodes a member of the AMP deaminase gene family. Additionally we are shipping AMPD3 Proteins (6) and AMPD3 Kits (4) and many more products for this protein.
Showing 10 out of 63 products:
Human Polyclonal AMPD3 Primary Antibody for EIA, WB - ABIN360232
Mahnke-Zizelman, Eddy, Shows, Sabina: Characterization of the human AMPD3 gene reveals that 5' exon useage is subject to transcriptional control by three tandem promoters and alternative splicing. in Biochimica et biophysica acta 1996
Show all 2 references for ABIN360232
mtDNA deletion coordinately induces AMP (show APRT Antibodies) deaminase to contribute to the loss of atrial adenine nucleotides through degrading AMP (show APRT Antibodies) excessively.
The primary underlying mechanism for increased catabolic flow through the AMP (show APRT Antibodies) deaminase reaction in circulating erythrocytes of individuals with familial phosphofructokinase deficiency is Ca2 (show CA2 Antibodies)+-calmodulin (show CALM1 Antibodies) activation of AMP deaminase isoform E.
may control the systemic metabolic status by changing AMPK (show PRKAA1 Antibodies) activity through the AMP (show APRT Antibodies) level.
This is a first report evidencing the pattern of AMPD (show AMPD1 Antibodies) genes expression in neoplastic human liver.
Erythrocytes from Ampd3(-/-) mice exhibited higher half-saturation pressure of oxygen.
effect of AMP-deaminase 3 knock-out in mice on enzyme activity in heart and other organs
AMP (show TMPRSS5 Antibodies) deaminase-deficient models demonstrate for the first time that AMPD3 plays a critical role in remote reperfusion lung injury via generation of inosine monophosphate (IMP (show BRAP Antibodies)).
AMPD3 deficiency increases the level of ATP in erythrocytes, but does not improve anemia due to pyruvate kinase deficiency and leads to erythrocyte dysfunction.
Along with the activation of AMPD3, ischemia-reperfusion-induced lung inflammation is associated with increased MPO (show MPO Antibodies) activity and TNF-alpha (show TNF Antibodies) level.
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.
adenosine monophosphate deaminase (isoform E)
, AMP deaminase 3
, adenosine monophosphate deaminase 3
, erythrocyte adenosine monophosphate deaminase
, AMP deaminase 3-like
, AMP aminohydrolase
, erythrocyte AMP deaminase
, erythrocyte type AMP deaminase
, erythrocyte-specific AMP deaminase
, myoadenylate deaminase
, AMP deaminase H-type
, heart-type AMPD