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Adenosine Monophosphate Deaminase 1 (AMPD1) ELISA Kits

Adenosine monophosphate deaminase 1 catalyzes the deamination of AMP to IMP in skeletal muscle and plays an important role in the purine nucleotide cycle. Additionally we are shipping Adenosine Monophosphate Deaminase 1 Antibodies (75) and Adenosine Monophosphate Deaminase 1 Proteins (5) and many more products for this protein.

list all ELISA KIts Gene Name GeneID UniProt
Anti-Human AMPD1 AMPD1 270 P23109
Anti-Mouse AMPD1 AMPD1 229665  
Anti-Rat AMPD1 AMPD1 25028 P10759
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More ELISA Kits for Adenosine Monophosphate Deaminase 1 Interaction Partners

Human Adenosine Monophosphate Deaminase 1 (AMPD1) interaction partners

  1. Variations in AMPD1, CPT2 (show CPT2 ELISA Kits), and PGYM genes are not associated with the onset, susceptibility, or severity of chronic fatigue syndrome.

  2. Common polymorphism of the AMPD1 gene (C34T) is strongly associated with essential hypertension.

  3. AMPD1 could have a profound influence on cholinergic neurotransmission and sleep; further studies are mandatory

  4. AMPD1 34C>T variant is associated with higher infection susceptibility to community acquired pneumonia but not to ventilator associated pneumonia in sepsis pateints

  5. Mutational variants in AMPD1 contribute to autism risk in Han Chinese population, via mitochondria dysfunction and cell necrosis.

  6. The best response to creatine in terms of physical performance was presented by AMPD1 CC genotype.

  7. The present study demonstrated a positive effect of C34T AMPD1 gene polymorphism in aortic stiffness and in inflammatory status in a high risk population of CAD (show CAD ELISA Kits) subjects.

  8. Our other studies on the metabolic impact of AMPD1 C34T mutation revealed decrease in AMPD activity.

  9. AMPD1 gene polymorphism C34T can be considered as a marker of liability to the high-speed and strength muscular activity.

  10. In a study of a Spanish and 2 North African cohorts, frequency of the AMPD1 C34T mutation was lower in Berbers compared with the Alpujarra cohort. The GDF8 (show MSTN ELISA Kits) K153R substitution showed little variability among the three cohorts.

Pig (Porcine) Adenosine Monophosphate Deaminase 1 (AMPD1) interaction partners

  1. The deduced amino acid sequence of AMPD1 contains an AMP (show TMPRSS5 ELISA Kits) deaminase signature sequence (SLSTDDP). RT-PCR analyses showed that AMPD1 was expressed specifically in skeletal muscle.

Cow (Bovine) Adenosine Monophosphate Deaminase 1 (AMPD1) interaction partners

  1. Our results indicate that the deletion mutation in the AMPD1 gene is associated with production traits, and may be used for marker-assisted selection in beef cattle breeding programs.

  2. These results suggest that the 18-bp deletion mutation in AMPD1 may influence the carcass traits in Qinchuan cattle.

Mouse (Murine) Adenosine Monophosphate Deaminase 1 (AMPD1) interaction partners

  1. AMPD1 deficiency activates AMPK (show PRKAA1 ELISA Kits)/Akt (show AKT1 ELISA Kits)/mTORC1/p70 S6 kinase (show PRKACB ELISA Kits) axis in skeletal muscle after high fat diet challenge, but not in normal chow diet. These changes may contribute to improve insulin (show INS ELISA Kits) resistance.

  2. Disruption of the AMPD1 gene leads to a less severe state of insulin (show INS ELISA Kits) resistance, improved glucose tolerance and enhanced insulin (show INS ELISA Kits) clearance in mice fed a high-fat diet. Data suggest that AMPD may be a new drug target for reversing insulin (show INS ELISA Kits) resistance.

  3. AMPD1 deficiency is acquired prior to overt muscle inflammation and is responsible, at least in part, for the muscle weakness that occurs in the mouse model of myositis.

Adenosine Monophosphate Deaminase 1 (AMPD1) Antigen Profile

Antigen Summary

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.

Gene names and symbols associated with AMPD1

  • adenosine monophosphate deaminase 1 (AMPD1) antibody
  • N-acetyl-anhydromuranmyl-L-alanine amidase (ampD1) antibody
  • N-acetylmuramoyl-L-alanine amidase (ampD1) antibody
  • Negative regulator of beta-lactamase expression (ampD1) antibody
  • adenosine monophosphate deaminase 1 (ampd1) antibody
  • adenosine monophosphate deaminase 1 (Ampd1) antibody
  • adenosine monophosphate deaminase 1 (isoform M) (ampd1) antibody
  • AI553520 antibody
  • Ampd-1 antibody
  • Ampd01 antibody
  • ampd1 antibody
  • MAD antibody
  • MADA antibody
  • RATAMPD01 antibody
  • zgc:77905 antibody

Protein level used designations for AMPD1

N-acetyl-anhydromuranmyl-L-alanine amidase , N-acetylmuramoyl-L-alanine amidase , Negative regulator of beta-lactamase expression , adenosine monophosphate deaminase 1 , AMP deaminase 1-like , adenosine monophosphate deaminase 1 (isoform M) , AMP deaminase 1 , AMPD , adenosine monophosphate deaminase-1 (muscle) , myoadenylate deaminase , skeletal muscle AMPD , Ampd

GENE ID SPECIES
100065374 Equus caballus
2766844 Yersinia pestis biovar Microtus str. 91001
4607045 Azoarcus sp. BH72
7815531 Rickettsia africae ESF-5
100196648 Salmo salar
100414418 Callithrix jacchus
100445019 Pongo abelii
100344490 Oryctolagus cuniculus
100540618 Meleagris gallopavo
100552392 Anolis carolinensis
100590300 Nomascus leucogenys
270 Homo sapiens
606901 Canis lupus familiaris
100101472 Sus scrofa
512748 Bos taurus
229665 Mus musculus
25028 Rattus norvegicus
457144 Pan troglodytes
772125 Gallus gallus
393867 Danio rerio
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