DNAJC19 Protein (Myc-DYKDDDDK Tag)

Produktnummer ABIN2719602

Produktdetails

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

Protein-Typ: Recombinant

Spezies: Human

Quelle: HEK-293 Cells

Aufreinigungstag / Konjugat: Dieses DNAJC19 Protein ist gelabelt mit Myc-DYKDDDDK Tag.

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

Produktmerkmale:

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

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

Anwendungsinformationen

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

Kommentare:

The tag is located at the C-terminal.

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Konzentration: 50 μg/mL

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

Lagerung: -80 °C

Informationen zur Lagerung: 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.

Antigendetails

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

Andere Bezeichnung: Dnajc19,tim14 (DNAJC19 Produkte)

Synonyme: 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

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: 12.3 kDa

NCBI Accession: NP_660304

Pathways: SARS-CoV-2 Protein Interaktom