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WFS1 Polyklonaler Antikörper
WFS1 Polyklonal Antikörper für IHC, IF/ICC, IF-P, IF-Fro, Indirect ELISA
Wirt / Isotyp
Kaninchen / IgG
Getestete Reaktivität
human, Maus, Ratte
Anwendung
IHC, IF/ICC, IF-P, IF-Fro, Indirect ELISA
Konjugation
Unkonjugiert
Kat-Nr. : 26995-1-PBS
Synonyme
Geprüfte Anwendungen
Produktinformation
26995-1-PBS bindet in IHC, IF/ICC, IF-P, IF-Fro, Indirect ELISA WFS1 und zeigt Reaktivität mit human, Maus, Ratten
Getestete Reaktivität | human, Maus, Ratte |
Wirt / Isotyp | Kaninchen / IgG |
Klonalität | Polyklonal |
Typ | Antikörper |
Immunogen | WFS1 fusion protein Ag25724 |
Vollständiger Name | Wolfram syndrome 1 (wolframin) |
Berechnetes Molekulargewicht | 890 aa, 100 kDa |
Beobachtetes Molekulargewicht | |
GenBank-Zugangsnummer | BC030130 |
Gene symbol | WFS1 |
Gene ID (NCBI) | 7466 |
Konjugation | Unkonjugiert |
Form | Liquid |
Reinigungsmethode | Antigen-Affinitätsreinigung |
Lagerungspuffer | PBS only |
Lagerungsbedingungen | Store at -80°C. 20ul Größen enthalten 0,1% BSA. |
Hintergrundinformationen
Wolfram syndrome protein (WFS1), also called wolframin, is a transmembrane protein, which is located primarily in the endoplasmic reticulum and its expression is induced in response to ER stress, partially through transcriptional activation. ER localization suggests that WFS1 protein has physiological functions in membrane trafficking, secretion, processing and/or regulation of ER calcium homeostasis. It is ubiquitously expressed with highest levels in brain, pancreas, heart, and insulinoma beta-cell lines. Mutations of the WFS1 gene are responsible for two hereditary diseases, autosomal recessive Wolfram syndrome and autosomal dominant low frequency sensorineural hearing loss. Wolframin assembles into higher molecular weight complexes of approximately 400 kDa in the membrane(PMID: 12913071)