anti-Adenosine Monophosphate Deaminase 1 (AMPD1) Anticorps

Adenosine monophosphate deaminase 1 catalyzes the deamination of AMP to IMP in skeletal muscle and plays an important role in the purine nucleotide cycle. De plus, nous expédions Adenosine Monophosphate Deaminase 1 Protéines (5) et et beaucoup plus de produits pour cette protéine.

afficher tous les anticorps Gène GeneID UniProt
AMPD1 270 P23109
AMPD1 229665  
AMPD1 25028 P10759
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Top anti-Adenosine Monophosphate Deaminase 1 Anticorps sur anticorps-enligne.fr

Showing 10 out of 92 products:

Catalogue No. Reactivité Hôte Conjugué Application Images Quantité Livraison Prix Détails
Humain Chèvre Inconjugué ELISA   100 μg 6 to 7 Days
$291.53
Détails
Humain Lapin Inconjugué IHC, ELISA Immunohistochemistry analysis of paraffin-embedded human thyroid gland tissue, using AMPD1 Antibody. The picture on the right is treated with the synthesized peptide. 100 μg 2 to 3 Days
$302.50
Détails
Boeuf (Vache) Lapin Inconjugué WB Host:  Rabbit  Target Name:  AMPD1  Sample Type:  293T Whole Cell lysates  Antibody Dilution:  1.0ug/ml 100 μL 2 to 3 Days
$289.00
Détails
Boeuf (Vache) Lapin Inconjugué IHC, IHC (p), WB Human Skeletal Muscle (formalin-fixed, paraffin-embedded) stained with AMPD1 antibody ABIN294609 at 10 ug/ml followed by biotinylated goat anti-rabbit IgG secondary antibody ABIN481713, alkaline phosphatase-streptavidin and chromogen. Anti-AMPD1 antibody IHC of human skeletal muscle. Immunohistochemistry of formalin-fixed, paraffin-embedded tissue after heat-induced antigen retrieval. Antibody concentration 10 ug/ml. 50 μg 11 to 14 Days
$484.00
Détails
Boeuf (Vache) Lapin Inconjugué IHC, IHC (p), WB Human Skeletal Muscle (formalin-fixed, paraffin-embedded) stained with AMPD1 antibody ABIN294610 at 5-10 ug/ml followed by biotinylated goat anti-rabbit IgG secondary antibody ABIN481713, alkaline phosphatase-streptavidin and chromogen. Anti-AMPD1 antibody IHC of human skeletal muscle. Immunohistochemistry of formalin-fixed, paraffin-embedded tissue after heat-induced antigen retrieval. Antibody concentration 10 ug/ml. 50 μg 11 to 14 Days
$484.00
Détails
Chimpanzé Lapin Inconjugué IHC (p), WB 50 μg 6 to 8 Days
$495.00
Détails
Chimpanzé Lapin Inconjugué IHC (p), WB 50 μg 6 to 8 Days
$495.00
Détails
Humain Lapin Inconjugué IHC, ELISA 100 μL 11 to 14 Days
$419.83
Détails
Humain Lapin Inconjugué IHC, WB Western blot analysis of extracts of various cells, using AMPD1 antibody. Immunohistochemistry of paraffin-embedded human esophagus using AMPD1 antibody. 100 μL 11 to 13 Days
$366.77
Détails
Humain Lapin Inconjugué IF (p), IHC (p), WB Formalin-fixed and paraffin embedded rat cardiac muscle labeled with Rabbit Anti AMP deaminase 1 Polyclonal Antibody, Unconjugated (ABIN873205) at 1:200 followed by conjugation to the secondary antibody and DAB staining 100 μL 3 to 7 Days
$317.90
Détails

anti-Adenosine Monophosphate Deaminase 1 Anticorps mieux référencés

  1. Cow (Bovine) Polyclonal AMPD1 Primary Antibody pour ELISA - ABIN548066 : Hand, Roth, Roltsch, Park, Kostek, Ferrell, Brown: AMPD1 gene polymorphism and the vasodilatory response to ischemia. dans Life sciences 2006 (PubMed)

  2. Cow (Bovine) Polyclonal AMPD1 Primary Antibody pour IHC (p), WB - ABIN4280395 : Coley, Rayavarapu, Pandey, Sabina, Van der Meulen, Ampong, Wortmann, Rawat, Nagaraju: The molecular basis of skeletal muscle weakness in a mouse model of inflammatory myopathy. dans Arthritis and rheumatism 2012 (PubMed)

Plus d’anticorps contre Adenosine Monophosphate Deaminase 1 partenaires d’interaction

Rabbit Adenosine Monophosphate Deaminase 1 (AMPD1) interaction partners

  1. Characterization of the metallocenter of rabbit skeletal muscle AMP deaminase.

Human Adenosine Monophosphate Deaminase 1 (AMPD1) interaction partners

  1. T allele of AMPD1 gene C34T polymorphism may be correlated with LVEF, LVEDD and SBP, which plays a protective role in the cardiac functions and blood pressure in cardiovascular disease patients.

  2. The metabolic-chronotropic response is decreased in skeletal muscle MAD deficiency, suggesting a biological mechanism by which AMPD1 gene exerts cardiac effect

  3. Variations in AMPD1, CPT2, and PGYM genes are not associated with the onset, susceptibility, or severity of chronic fatigue syndrome.

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

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

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

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

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

  9. 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 subjects.

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

  11. Alpinists show significantly higher frequencies of T allele compared to controls.

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

  13. 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 K153R substitution showed little variability among the three cohorts.

  14. There was a lower frequency of the AMPD1 exon 2 T34 allele in elite Polish power-oriented athletes. The data suggested that the C allele may help athletes to attain elite status in power-oriented sports.

  15. The researchers found evidence that the T allele polymorphism of the AMPD1 gene is associated with negative factor in athletic performance

  16. AMPD1 gene mutations are associated with obesity and diabetes in Polish patients with cardiovascular diseases.

  17. some physico-chemical properties of AMP-deaminase isolated from cardiac muscle of a 10-year-old boy heterozygote for this mutation

  18. A G468T AMPD1 mutant allele contributes to the high incidence of myoadenylate deaminase deficiency in the Caucasian population.

  19. Significantly higher frequency of mutation among donors with healthy hearts used for transplantation. Lower frequency in dysfunctional donor hearts. Frequency of C34T mutation in chronic heart failure was not different. (Review)

  20. The AMPD1 C34T polymorphism influences transplant-free cardiovascular survival in the setting of ischemic left ventricular dysfunction.

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

  1. Two novel single nucleotide polymorphisms in the AMPD1 promoter region are associated with carcass traits.

  2. molecular cloning: the distribution of genotypes among Min pig, Yorkshire and Duroc are extremely significantly different

  3. The deduced amino acid sequence of AMPD1 contains an AMP 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 is an adenosine monophosphate deaminase that catalyzes the deamination of AMP to IMP. An elevated AMP level and almost complete lack of IMP was detected in the skeletal muscle of E18.5 Ampd1(tm1a/tm1a) mice.

  2. AMPD1 deficiency activates AMPK/Akt/mTORC1/p70 S6 kinase axis in skeletal muscle after high fat diet challenge, but not in normal chow diet. These changes may contribute to improve insulin resistance.

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

  4. 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) profil antigène

Profil protéine

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

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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