Pallidin Antikörper (AA 1-170)

Produktnummer ABIN1682201

Produktdetails anti-Pallidin Antikörper

Target: Pallidin (PLDN) (Pallidin Homolog (PLDN))

Bindungsspezifität: AA 1-170

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser Pallidin Antikörper ist unkonjugiert

Applikation: Western Blotting (WB)

Sequenz: MSVPGPSSPD GALTRPPYCL EAGEPTPGLS DTSPDEGLIE DLTIEDKAVE QLAEGLLSHY LPDLQRSKQA LQELTQNQVV LLDTLEQEIS KFKECHSMLD INALFAEAKH YHAKLVNIRK EMLMLHEKTS KLKKRALKLQ QKRQKEELER EQQREKEFER EKQLTARPAK

Kreuzreaktivität: Human, Maus, Ratte

Produktmerkmale: Polyclonal Antibodies

Aufreinigung: Affinity purification

Immunogen: Recombinant fusion protein containing a sequence corresponding to amino acids 1-170 of human BLOC1S6 (NP_036520.1).

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: WB,1:200 - 1:2000

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

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 Pallidin

Target: Pallidin (PLDN) (Pallidin Homolog (PLDN))

Andere Bezeichnung: BLOC1S6 (PLDN Produkte)

Synonyme: CG14133 antikoerper, Dmel\\CG14133 antikoerper, LOC100226487 antikoerper, pldn antikoerper, BLOS6 antikoerper, HPS9 antikoerper, PA antikoerper, PALLID antikoerper, PLDN antikoerper, Pldn antikoerper, BLOC-1 antikoerper, Stx13bp1 antikoerper, pa antikoerper, pallidin antikoerper, CG14133 gene product from transcript CG14133-RB antikoerper, biogenesis of lysosomal organelles complex 1 subunit 6 antikoerper, pallidin homolog (mouse) antikoerper, biogenesis of lysosomal organelles complex-1, subunit 6, pallidin antikoerper, Pallidin antikoerper, BLOC1S6 antikoerper, pldn antikoerper, Bloc1s6 antikoerper

Hintergrund: The protein encoded by this gene may play a role in intracellular vesicle trafficking. It interacts with Syntaxin 13 which mediates intracellular membrane fusion. Mutations in this gene cause symptoms associated with Hermansky-Pudlak syndrome-9. Alternative splicing results in multiple transcript variants. A pseudogene related to this gene is located on the X chromosome.,BLOC1S6,BLOS6,HPS9,PA,PALLID,PLDN,Signal Transduction,BLOC1S6

Molekulargewicht: 8 kDa/19 kDa

Gen-ID: 26258

UniProt: Q9UL45

Pathways: Synaptic Vesicle Exocytosis