DnaJ (Hsp40) Homolog, Subfamily C, Member 19 (DNAJC19) Peptide
DNAJC19
Reactivity: Mammalian
Host: Synthetic
BP, WB, IHC
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- Target See all DNAJC19 products
- DNAJC19 (DnaJ (Hsp40) Homolog, Subfamily C, Member 19 (DNAJC19))
- Peptide Type
- Synthetic
- Origin
- Mammalian
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Source
- Synthetic
- Application
- Blocking Peptide (BP), Western Blotting (WB), Immunohistochemistry (IHC)
- Sequence
- LGVSPTANKG KIRDAHRRIM LLNHPDKGGS PYIAAKINEA KDLLEGQAKK
- Characteristics
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A synthetic peptide for use as a blocking control in assays to test for specificity of DNAJC19 antibody,
Alternative Names: DNAJC19 control peptide, DNAJC19 antibody Blocking Peptide, Anti-DNAJC19 Blocking Peptide, DnaJ, Hsp40 homolog, subfamily C, member 19 Blocking Peptide, TIM14 Blocking Peptide, TIMM14 Blocking Peptide, DNAJC19, DNAJC-19, DNAJC 19, DNAJC-19 Blocking Peptide, DNAJC 19 Blocking Peptide
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- Application Notes
- Optimal conditions should be determined by the investigator
- Restrictions
- For Research Use only
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- Format
- Lyophilized
- Reconstitution
- Add 100 µL of distilled water for a final peptide concentration is 1 mg/mL.
- Buffer
- PBS
- Handling Advice
- Avoid repeated freeze/thaw cycles.
- Storage
- -20 °C
- Storage Comment
- Store at -20 °C long term.
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- Target
- DNAJC19 (DnaJ (Hsp40) Homolog, Subfamily C, Member 19 (DNAJC19))
- Synonyms
- PAM18 Peptide, TIM14 Peptide, TIMM14 Peptide, 1810055D05Rik Peptide, AA959924 Peptide, Tim14 Peptide, zgc:73251 Peptide, DNAJC19 Peptide, DKFZp469M2132 Peptide, Gm15118 Peptide, RGD1560220 Peptide, DnaJ heat shock protein family (Hsp40) member C19 Peptide, DnaJ (Hsp40) homolog, subfamily C, member 19 Peptide, DnaJ heat shock protein family (Hsp40) member C19 L homeolog Peptide, Pam18p Peptide, DnaJ heat shock protein family (Hsp40) member C19, pseudogene Peptide, DNAJC19 Peptide, Dnajc19 Peptide, dnajc19 Peptide, dnajc19.L Peptide, PAM18 Peptide, Dnajc19-ps Peptide
- 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). Several transcript variants, some protein-coding and some not, have been found for this gene.
- Molecular Weight
- 13 kDa
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