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Please note: We are reviewing Western blot images included in the antibody testing data in our catalog, including those provided by third parties. Unless expressly labeled or annotated as “raw-unedited”, Western blot images included in the antibody testing data in our catalog may have been edited, optimized or otherwise adjusted for presentation.
The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen and the purity is > 95% (by SDS-PAGE).
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. [provided by RefSeq, Jan 2012]
仅用于科研。不用于诊断过程。未经明确授权不得转售。
蛋白别名: DnaJ homolog subfamily C member 19; Mitochondrial import inner membrane translocase subunit TIM14
基因别名: 1810055D05Rik; AA959924; DNAJC19; RGD1560220; TIM14; TIMM14
UniProt ID: (Mouse) Q9CQV7
Entrez Gene ID: (Rat) 502525, (Mouse) 67713