DNAJC19 Antikörper

Produktnummer ABIN7261189

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), Immunohistochemistry (IHC), Immunofluorescence (IF)

Produktmerkmale: Polyclonal Antibody

Aufreinigung: Affinity purification

Immunogen: Recombinant fusion protein of human DNAJC19 (NP_660304.1).

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

Konzentration: 1 mg/mL

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 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: 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:

Observed_MW: 12 kDa

Calculated_MW: 10 kDa/12 kDa

Gen-ID: 131118

UniProt: Q96DA6

Pathways: SARS-CoV-2 Protein Interaktom