Dosaggi Vasopressin

13 prodotti

Vasopressin è un gene codificato dal simbolo AVP. È noto anche come: Vasopressin-neurophysin 2-copeptin; AVP-NPII; AVP; ARVP; VP. Vasopressin ha una massa di 17.33kDa, una lunghezza di amminoacidi di 164, ed è implicato in Diabetes insipidus, neurohypophyseal.

Offriamo 13 Vasopressin ELISA kit per il rilevamento qualitativo o quantitativo di Vasopressin da campioni di Umano, Topo, Ratto, Bovino, Maiale, Pecora e Cane.

Informazioni su geni e proteine

Riepilogo UniProt
Neurophysin 2 specifically binds vasopressin.
Sommario di Entrez
This gene encodes a member of the vasopressin/oxytocin family and preproprotein that is proteolytically processed to generate multiple protein products. These products include the neuropeptide hormone arginine vasopressin, and two other peptides, neurophysin 2 and copeptin. Arginine vasopressin is a posterior pituitary hormone that is synthesized in the supraoptic nucleus and paraventricular nucleus of the hypothalamus. Along with its carrier protein, neurophysin 2, it is packaged into neurosecretory vesicles and transported axonally to the nerve endings in the neurohypophysis where it is either stored or secreted into the bloodstream. The precursor is thought to be activated while it is being transported along the axon to the posterior pituitary. Arginine vasopressin acts as a growth factor by enhancing pH regulation through acid-base transport systems. It has a direct antidiuretic action on the kidney, and also causes vasoconstriction of the peripheral vessels. This hormone can contract smooth muscle during parturition and lactation. It is also involved in cognition, tolerance, adaptation and complex sexual and maternal behaviour, as well as in the regulation of water excretion and cardiovascular functions. Mutations in this gene cause autosomal dominant neurohypophyseal diabetes insipidus (ADNDI). This gene is present in a gene cluster with the related gene oxytocin on chromosome 20.
Coinvolgimento nella malattia
Diabetes insipidus, neurohypophyseal: A disease characterized by persistent thirst, polydipsia and polyuria. Affected individuals are apparently normal at birth, but characteristically develop symptoms of vasopressin deficiency during childhood.
Somiglianze di sequenza
Belongs to the vasopressin/oxytocin family.
Posizione cellulare
Secreted.
Standard Curve - Human Vasopressin ELISA Kit (A3138) - Antibodies.com
Standard Curve - Rat Vasopressin ELISA Kit (A7483) - Antibodies.com
Standard Curve - Vasopressin ELISA Kit (A86970) - Antibodies.com
Standard Curve - Human Copeptin ELISA Kit (A77912) - Antibodies.com
Standard Curve - Human Antidiuretic Hormone ELISA Kit (A77639) - Antibodies.com
Standard Curve - Canine Antidiuretic Hormone ELISA Kit (A326336) - Antibodies.com
Standard Curve - Rat Copeptin ELISA Kit (A75110) - Antibodies.com
Standard Curve - Porcine Copeptin ELISA Kit (A87192) - Antibodies.com
Standard Curve - Mouse Vasopressin ELISA Kit (A5483) - Antibodies.com
Standard Curve - Rat Antidiuretic Hormone ELISA Kit (A79874) - Antibodies.com
Standard Curve - Bovine Antidiuretic Hormone ELISA Kit (A87434) - Antibodies.com
Standard Curve - Sheep Antidiuretic Hormone ELISA Kit (A87523) - Antibodies.com
Standard Curve - Mouse Antidiuretic Hormone ELISA Kit (A77640) - Antibodies.com

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