DNAJC19 anticorps

N° du produit ABIN7113588

Détail du produit anti-DNAJC19 anticorps

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

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp DNAJC19 est non-conjugé

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

Purification: Immunogen affinity purified

Pureté: ≥95 % as determined by SDS-PAGE

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

Isotype: IgG

Information d'application

Indications d'application: WB: 1:500 - 1:2000, IHC: 1:50 - 1:200, IF: 1:50 - 1:200

Restrictions: For Research Use only

Stockage

Format: Liquid

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

Agent conservateur: Sodium azide

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

Stock: -20 °C

Stockage commentaire: -20°C for 12 months (Avoid repeated freeze / thaw cycles.)

Date de péremption: 12 months

Détails sur DNAJC19

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

Autre désignation: DNAJC19 (DNAJC19 Produits)

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

Sujet: 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.

Poids moléculaire: 12 kDa

ID gène: 131118

UniProt: Q96DA6

Pathways: SARS-CoV-2 Protein Interactome