DNAJC19 antibody
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Description
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.
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Product specifications
| Category | Primary Antibodies |
| Immunogen Target | DnaJ (Hsp40) homolog, subfamily C, member 19 (DNAJC19) |
| Host | Rabbit |
| Reactivity | Human, Mouse, Rat |
| Recommended Dilution | WB: 1:500 - 1:2000; IHC: 1:50 - 1:200; IF: 1:50 - 1:200 |
| Clonality | polyclonal |
| Conjugation | Unconjugated |
| Isotype | IgG |
| Observed MW | 12 kDa |
| Purity | ≥95% as determined by SDS-PAGE |
| Purification | Immunogen affinity purified |
| Size 1 | 100µg |
| Form | liquid |
| Tested Applications | ELISA, WB, IHC, IF |
| Storage | PBS with 0.02% sodium azide and 50% glycerol pH 7.3, -20℃ for 12 months (Avoid repeated freeze / thaw cycles.) |
| UniProt ID | Q96DA6 |
| Gene ID | 131118 |
| Alias | Mitochondrial import inner membrane translocase subunit TIM14,DnaJ homolog subfamily C member 19,DNAJC19,TIM14,TIMM14 |
| Background | Antibody anti-DNAJC19 |
| Status | RUO |
| Note | Mol. Weight 12 kDa |
Descripción
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