DNAJC19 Protein (Myc-DYKDDDDK Tag)

N° du produit ABIN2719602

Détail du produit

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

Type de proteíne: Recombinant

Origine: Humain

Source: HEK-293 Cells

Purification/Conjugué: Cette DNAJC19 protéine est marqué à la Myc-DYKDDDDK Tag.

Application: Antibody Production (AbP), Standard (STD)

Attributs du produit:

• Recombinant human DNAJC19 / TIM14 protein expressed in HEK293 cells.
• Produced with end-sequenced ORF clone

Pureté: > 80 % as determined by SDS-PAGE and Coomassie blue staining

Information d'application

Indications d'application: Recombinant human proteins can be used for:
Native antigens for optimized antibody production
Positive controls in ELISA and other antibody assays

Commentaires:

The tag is located at the C-terminal.

Restrictions: For Research Use only

Stockage

Concentration: 50 μg/mL

Buffer: 25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10 % glycerol.

Stock: -80 °C

Stockage commentaire: Store at -80°C. Thaw on ice, aliquot to individual single-use tubes, and then re-freeze immediately. Only 2-3 freeze thaw cycles are recommended.

Détail du antigène

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

Autre désignation: Dnajc19,tim14 (DNAJC19 Produits)

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

Sujet: 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: 12.3 kDa

NCBI Accession: NP_660304

Pathways: SARS-CoV-2 Protein Interactome