Descrizione Azione

Subunit of the peripheral V1 complex of vacuolar ATPase essential for assembly or catalytic function. V-ATPase is responsible for acidifying a variety of intracellular compartments in eukaryotic cells. This isoform is essential for energy coupling involved in acidification of acrosome .Specific expression in testes.

Codice: E-AB-18425_20μL Confezionamento: 20μL
Dettagli

Subunit of the peripheral V1 complex of vacuolar ATPase essential for assembly or catalytic function. V-ATPase is responsible for acidifying a variety of intracellular compartments in eukaryotic cells. This isoform is essential for energy coupling involved in acidification of acrosome .Specific expression in testes.

Codice: E-AB-18425_60μL Confezionamento: 60μL
Dettagli

Subunit of the peripheral V1 complex of vacuolar ATPase essential for assembly or catalytic function. V-ATPase is responsible for acidifying a variety of intracellular compartments in eukaryotic cells. This isoform is essential for energy coupling involved in acidification of acrosome .Specific expression in testes.

Codice: E-AB-18425_200μL Confezionamento: 200μL
Dettagli

Subunit of the peripheral V1 complex of vacuolar ATPase essential for assembly or catalytic function. V-ATPase is responsible for acidifying a variety of intracellular compartments in eukaryotic cells. This isoform is essential for energy coupling involved in acidification of acrosome .Specific expression in testes.

Codice: E-AB-18425_120μL Confezionamento: 120μL
Dettagli

A synthesized peptide derived from human ATP6V1G1.

Codice: DF15477 Confezionamento: 100ul
Dettagli

A synthesized peptide derived from human ATP6V1G3, corresponding to a region within the internal amino acids.

Codice: DF10005 Confezionamento: 100ul
Dettagli

A synthesized peptide derived from human ATP7A, corresponding to a region within C-terminal amino acids.

Codice: DF8506 Confezionamento: 100ul
Dettagli

This gene encodes a transmembrane protein that functions in copper transport across membranes. This protein is localized to the trans Golgi network, where it is predicted to supply copper to copper-dependent enzymes in the secretory pathway. It relocalizes to the plasma membrane under conditions of elevated extracellular copper, and functions in the efflux of copper from cells. Mutations in this gene are associated with Menkes disease, X-linked distal spinal muscular atrophy, and occipital horn syndrome. Alternatively-spliced transcript variants have been observed.

Codice: E-AB-16268_60μL Confezionamento: 60μL
Dettagli

This gene encodes a transmembrane protein that functions in copper transport across membranes. This protein is localized to the trans Golgi network, where it is predicted to supply copper to copper-dependent enzymes in the secretory pathway. It relocalizes to the plasma membrane under conditions of elevated extracellular copper, and functions in the efflux of copper from cells. Mutations in this gene are associated with Menkes disease, X-linked distal spinal muscular atrophy, and occipital horn syndrome. Alternatively-spliced transcript variants have been observed.

Codice: E-AB-16268_20μL Confezionamento: 20μL
Dettagli

This gene encodes a transmembrane protein that functions in copper transport across membranes. This protein is localized to the trans Golgi network, where it is predicted to supply copper to copper-dependent enzymes in the secretory pathway. It relocalizes to the plasma membrane under conditions of elevated extracellular copper, and functions in the efflux of copper from cells. Mutations in this gene are associated with Menkes disease, X-linked distal spinal muscular atrophy, and occipital horn syndrome. Alternatively-spliced transcript variants have been observed.

Codice: E-AB-16268_200μL Confezionamento: 200μL
Dettagli

This gene encodes a transmembrane protein that functions in copper transport across membranes. This protein is localized to the trans Golgi network, where it is predicted to supply copper to copper-dependent enzymes in the secretory pathway. It relocalizes to the plasma membrane under conditions of elevated extracellular copper, and functions in the efflux of copper from cells. Mutations in this gene are associated with Menkes disease, X-linked distal spinal muscular atrophy, and occipital horn syndrome. Alternatively-spliced transcript variants have been observed.

Codice: E-AB-16268_120μL Confezionamento: 120μL
Dettagli

A synthesized peptide derived from human ATP7B, corresponding to a region within C-terminal amino acids.

Codice: AF0410 Confezionamento: 100ul
Dettagli