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AMIGO3 Antibody detects endogenous levels of AMIGO3.

Codice: DF15995 Confezionamento: 200ul
Dettagli

AMIGO3 Antibody detects endogenous levels of AMIGO3.

Codice: DF15995 Confezionamento: 100ul
Dettagli

Amino-terminal enhancer of split Antibody detects endogenous levels of total Amino-terminal enhancer of split.

Codice: DF13613 Confezionamento: 200ul
Dettagli

Amino-terminal enhancer of split Antibody detects endogenous levels of total Amino-terminal enhancer of split.

Codice: DF13613 Confezionamento: 100ul
Dettagli

AMOT Antibody detects endogenous levels of total AMOT.

Codice: DF9208 Confezionamento: 200ul
Dettagli

AMOT Antibody detects endogenous levels of total AMOT.

Codice: DF9208 Confezionamento: 100ul
Dettagli

AMOTL1 Antibody detects endogenous levels of total AMOTL1.

Codice: DF12556 Confezionamento: 200ul
Dettagli

AMOTL1 Antibody detects endogenous levels of total AMOTL1.

Codice: DF12556 Confezionamento: 100ul
Dettagli

AMPD1 Antibody detects endogenous levels of AMPD1.

Codice: DF15771 Confezionamento: 100ul
Dettagli

AMPD1 Antibody detects endogenous levels of AMPD1.

Codice: DF15771 Confezionamento: 200ul
Dettagli

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.

Codice: E-AB-12967_60μL Confezionamento: 60μL
Dettagli

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.

Codice: E-AB-12967_200μL Confezionamento: 200μL
Dettagli