BCAP31 Antikörper (AA 127-246)

Produktnummer ABIN6137477

Der Kaninchen Polyklonal Anti-BCAP31-Antikörper wurde für WB, IF und IP validiert. Er ist geeignet, BCAP31 in Proben von Human zu detektieren.

Kurzübersicht für BCAP31 Antikörper (AA 127-246) (ABIN6137477)

Target: BCAP31 (B-Cell Receptor-Associated Protein 31 (BCAP31))

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser BCAP31 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB), Immunofluorescence (IF), Immunoprecipitation (IP)

Produktdetails anti-BCAP31 Antikörper

Bindungsspezifität: AA 127-246

Sequenz: ATLLASNEAF KKQAESASEA AKKYMEENDQ LKKGAAVDGG KLDVGNAEVK LEEENRSLKA DLQKLKDELA STKQKLEKAE NQVLAMRKQS EGLTKEYDRL LEEHAKLQAA VDGPMDKKEE

Kreuzreaktivität: Human, Maus, Ratte

Produktmerkmale: Polyclonal Antibodies

Aufreinigung: Affinity purification

Immunogen: Recombinant fusion protein containing a sequence corresponding to amino acids 127-246 of human BAP31 (NP_001243376.1).

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: WB,1:500 - 1:2000,IF,1:50 - 1:100,IP,1:50 - 1:100

Kommentare:

HIGH QUALITY

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Buffer: PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.

Konservierungsmittel: Sodium azide

Vorsichtsmaßnahmen: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Lagerung: -20 °C

Informationen zur Lagerung: Store at -20°C. Avoid freeze / thaw cycles.

Details zu BCAP31

Target: BCAP31 (B-Cell Receptor-Associated Protein 31 (BCAP31))

Andere Bezeichnung: BCAP31

Hintergrund: This gene encodes a member of the B-cell receptor associated protein 31 superfamily. The encoded protein is a multi-pass transmembrane protein of the endoplasmic reticulum that is involved in the anterograde transport of membrane proteins from the endoplasmic reticulum to the Golgi and in caspase 8-mediated apoptosis. Microdeletions in this gene are associated with contiguous ABCD1/DXS1375E deletion syndrome (CADDS), a neonatal disorder. Alternative splicing of this gene results in multiple transcript variants. Two related pseudogenes have been identified on chromosome 16.,BCAP31,6C6-AG,BAP31,CDM,DDCH,DXS1357E,Signal Transduction,PI3K-Akt Signaling Pathway,Cell Biology & Developmental Biology,Apoptosis,BCAP31

Molekulargewicht: 27 kDa/34 kDa

Gen-ID: 10134

UniProt: P51572

Pathways: Positive Regulation of Endopeptidase Activity