DNAJC19 Protein (Myc-DYKDDDDK Tag)
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- Target See all DNAJC19 Proteins
- DNAJC19 (DnaJ (Hsp40) Homolog, Subfamily C, Member 19 (DNAJC19))
- Protein Type
- Recombinant
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Origin
- Human
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Source
- HEK-293 Cells
- Purification tag / Conjugate
- This DNAJC19 protein is labelled with Myc-DYKDDDDK Tag.
- Application
- Antibody Production (AbP), Standard (STD)
- Characteristics
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- Recombinant human DNAJC19 / TIM14 protein expressed in HEK293 cells.
- Produced with end-sequenced ORF clone
- Purity
- > 80 % as determined by SDS-PAGE and Coomassie blue staining
- Top Product
- Discover our top product DNAJC19 Protein
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- Application Notes
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Recombinant human proteins can be used for:
Native antigens for optimized antibody production
Positive controls in ELISA and other antibody assays - Comment
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The tag is located at the C-terminal.
- Restrictions
- For Research Use only
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- Concentration
- 50 μg/mL
- Buffer
- 25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10 % glycerol.
- Storage
- -80 °C
- Storage Comment
- 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.
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- Target
- DNAJC19 (DnaJ (Hsp40) Homolog, Subfamily C, Member 19 (DNAJC19))
- Alternative Name
- Dnajc19,tim14 (DNAJC19 Products)
- Synonyms
- 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
- 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.
- Molecular Weight
- 12.3 kDa
- NCBI Accession
- NP_660304
- Pathways
- SARS-CoV-2 Protein Interactome
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