DNAJC19 Antikörper

Produktnummer ABIN7113588

Produktdetails anti-DNAJC19 Antikörper

Target: DNAJC19 (DnaJ (Hsp40) Homolog, Subfamily C, Member 19 (DNAJC19))

Reaktivität: Human, Maus, Ratte

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser DNAJC19 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB), ELISA, Immunohistochemistry (IHC), Immunofluorescence (IF)

Aufreinigung: Immunogen affinity purified

Reinheit: ≥95 % as determined by SDS-PAGE

Immunogen: DnaJ (Hsp40) homolog, subfamily C, member 19

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: WB: 1:500 - 1:2000, IHC: 1:50 - 1:200, IF: 1:50 - 1:200

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Buffer: PBS with 0.02 % sodium azide and 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: -20°C for 12 months (Avoid repeated freeze / thaw cycles.)

Haltbarkeit: 12 months

Details zu DNAJC19

Target: DNAJC19 (DnaJ (Hsp40) Homolog, Subfamily C, Member 19 (DNAJC19))

Andere Bezeichnung: DNAJC19 (DNAJC19 Produkte)

Synonyme: PAM18 antikoerper, TIM14 antikoerper, TIMM14 antikoerper, 1810055D05Rik antikoerper, AA959924 antikoerper, Tim14 antikoerper, zgc:73251 antikoerper, DNAJC19 antikoerper, DKFZp469M2132 antikoerper, Gm15118 antikoerper, RGD1560220 antikoerper, DnaJ heat shock protein family (Hsp40) member C19 antikoerper, DnaJ (Hsp40) homolog, subfamily C, member 19 antikoerper, DnaJ heat shock protein family (Hsp40) member C19 L homeolog antikoerper, Pam18p antikoerper, DnaJ heat shock protein family (Hsp40) member C19, pseudogene antikoerper, DNAJC19 antikoerper, Dnajc19 antikoerper, dnajc19 antikoerper, dnajc19.L antikoerper, PAM18 antikoerper, Dnajc19-ps antikoerper

Hintergrund: Synonyms:TIM14, TIMM14 Background:The protein encoded by this gene is thought to be part of a complex involved in the ATP-dependent transport of transit peptide-containing proteins from the inner cell membrane to the mitochondrial matrix. Defects in this gene are a cause of 3-methylglutaconic aciduria type 5 (MGA5), also known as dilated cardiomyopathy with ataxia (DCMA). Alternative splicing of this gene results in multiple transcript variants. Related pseudogenes have been identified on chromosomes 1, 2, 6, 10, 14 and 19.

Molekulargewicht: 12 kDa

Gen-ID: 131118

UniProt: Q96DA6

Pathways: SARS-CoV-2 Protein Interaktom