ATP2C1 Antikörper (C-Term)

Produktnummer ABIN1537638

Produktdetails anti-ATP2C1 Antikörper

Target: ATP2C1 (ATPase, Ca++ Transporting, Type 2C, Member 1 (ATP2C1))

Bindungsspezifität: AA 882-909, C-Term

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser ATP2C1 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB)

Aufreinigung: This antibody is purified through a protein A column, followed by peptide affinity purification.

Immunogen: This ATP2C1 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 882-909 amino acids from the C-terminal region of human ATP2C1.

Klon: RB36281

Isotyp: Ig Fraction

Anwendungsinformationen

Applikationshinweise: WB: 1:1000

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Buffer: Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.

Konservierungsmittel: Sodium azide

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

Lagerung: 4 °C,-20 °C

Informationen zur Lagerung: ATP2C1 Antibody (C-term) can be refrigerated at 2-8 °C for up to 6 months. For long term storage, keep at -20 °C.

Haltbarkeit: 6 months

Details zu ATP2C1

Target: ATP2C1 (ATPase, Ca++ Transporting, Type 2C, Member 1 (ATP2C1))

Andere Bezeichnung: ATP2C1 (ATP2C1 Produkte)

Synonyme: ATP2C1 antikoerper, ATP2C1A antikoerper, BCPM antikoerper, HHD antikoerper, PMR1 antikoerper, SPCA1 antikoerper, hSPCA1 antikoerper, Spca1 antikoerper, si:dkey-11p23.6 antikoerper, SPCA antikoerper, 1700121J11Rik antikoerper, AW061228 antikoerper, D930003G21Rik antikoerper, pmr1 antikoerper, ATPase secretory pathway Ca2+ transporting 1 antikoerper, ATPase, Ca++ transporting, type 2C, member 1 antikoerper, ATPase, Ca++-sequestering antikoerper, ATP2C1 antikoerper, atp2c1 antikoerper, Atp2c1 antikoerper

Hintergrund: The protein encoded by this gene belongs to the family of P-type cation transport ATPases. This magnesium-dependent enzyme catalyzes the hydrolysis of ATP coupled with the transport of the calcium. Defects in this gene cause Hailey-Hailey disease, an autosomal dominant disorder. Alternatively spliced transcript variants encoding different isoforms have been identified.

Molekulargewicht: 100577

Gen-ID: 27032

NCBI Accession: NP_001001485, NP_001001486, NP_001001487, NP_001186108, NP_001186109, NP_001186110, NP_001186111, NP_001186112, NP_001186113, NP_001186114, NP_055197

UniProt: P98194

Pathways: Transition Metal Ion Homeostasis, Ribonucleoside Biosynthetic Process