Descrizione Azione
Codice: PDER100107_100μg Confezionamento: 100μg
Dettagli
Codice: PDER100107_500μg Confezionamento: 500μg
Dettagli
Codice: PDER100107_20μg Confezionamento: 20μg
Dettagli
Codice: PDER100107_1mg Confezionamento: 1mg
Dettagli
Codice: PDER100106_100μg Confezionamento: 100μg
Dettagli
Codice: PDER100106_1mg Confezionamento: 1mg
Dettagli
Codice: PDER100106_20μg Confezionamento: 20μg
Dettagli
Codice: PDER100106_500μg Confezionamento: 500μg
Dettagli

Degrades extracellular matrix. Proposed to play a role in breast cancer invasion and metastasis. Exhibits trypsin-like activity as defined by cleavage of synthetic substrates with Arg or Lys as the P1 site.Defects in ST14 are a cause of ichthyosis autosomal recessive with hypotrichosis (ARIH). ARIH is a skin disorder characterized by congenital ichthyosis associated with the presence of less than the normal amount of hair.

Codice: PDER100225_500μg Confezionamento: 500μg
Dettagli

Degrades extracellular matrix. Proposed to play a role in breast cancer invasion and metastasis. Exhibits trypsin-like activity as defined by cleavage of synthetic substrates with Arg or Lys as the P1 site.Defects in ST14 are a cause of ichthyosis autosomal recessive with hypotrichosis (ARIH). ARIH is a skin disorder characterized by congenital ichthyosis associated with the presence of less than the normal amount of hair.

Codice: PDER100225_100μg Confezionamento: 100μg
Dettagli

Degrades extracellular matrix. Proposed to play a role in breast cancer invasion and metastasis. Exhibits trypsin-like activity as defined by cleavage of synthetic substrates with Arg or Lys as the P1 site.Defects in ST14 are a cause of ichthyosis autosomal recessive with hypotrichosis (ARIH). ARIH is a skin disorder characterized by congenital ichthyosis associated with the presence of less than the normal amount of hair.

Codice: PDER100225_1mg Confezionamento: 1mg
Dettagli

Degrades extracellular matrix. Proposed to play a role in breast cancer invasion and metastasis. Exhibits trypsin-like activity as defined by cleavage of synthetic substrates with Arg or Lys as the P1 site.Defects in ST14 are a cause of ichthyosis autosomal recessive with hypotrichosis (ARIH). ARIH is a skin disorder characterized by congenital ichthyosis associated with the presence of less than the normal amount of hair.

Codice: PDER100225_20μg Confezionamento: 20μg
Dettagli