Abhydrolase Domain Containing 5 (ABHD5) Peptide
ABHD5
Reactivity: Human
Host: Synthetic
BP, WB
Catalog No. ABIN972756
Quick Overview for Abhydrolase Domain Containing 5 (ABHD5) Peptide (ABIN972756)
Target
ABHD5
(Abhydrolase Domain Containing 5 (ABHD5))
Origin
Human
Source
Synthetic
Application
Blocking Peptide (BP), Western Blotting (WB)
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Characteristics
- This is a synthetic peptide designed for use in combination with anti-ABHD5 antibody (Catalog #: ARP42455_T100). It may block above mentioned antibody from binding to its target protein in western blot and/or immunohistochecmistry under proper experimental settings. There is no guarantee for its use in other applications.
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Purification
- Purified
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Application Notes
- Each Investigator should determine their own optimal working dilution for specific applications.
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Restrictions
- For Research Use only
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Format
- Lyophilized
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Reconstitution
- Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.
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Concentration
- 1 mg/mL
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Buffer
- Final peptide concentration is 1 mg/mL in PBS.
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Handling Advice
- Avoid repeated freeze-thaw cycles.
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Storage
- -20 °C
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Storage Comment
- For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
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- ABHD5 (Abhydrolase Domain Containing 5 (ABHD5))
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Background
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ABHD5 belongs to a large family of proteins defined by an alpha/beta hydrolase fold, and contains three sequence motifs that correspond to a catalytic triad found in the esterase/lipase/thioesterase subfamily. It differs from other members of this subfamily in that its putative catalytic triad contains an asparagine instead of the serine residue. Mutations in ABHD5 gene have been associated with Chanarin-Dorfman syndrome, a triglyceride storage disease with impaired long-chain fatty acid oxidation.The protein encoded by this gene belongs to a large family of proteins defined by an alpha/beta hydrolase fold, and contains three sequence motifs that correspond to a catalytic triad found in the esterase/lipase/thioesterase subfamily. It differs from other members of this subfamily in that its putative catalytic triad contains an asparagine instead of the serine residue. Mutations in this gene have been associated with Chanarin-Dorfman syndrome, a triglyceride storage disease with impaired long-chain fatty acid oxidation.
Alias Symbols: CDS, CGI58, IECN2, MGC8731, NCIE2
Protein Interaction Partner: PLIN1,PLIN2
Protein Size: 349 -
Molecular Weight
- 39 kDa
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Gene ID
- 51099
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NCBI Accession
- NM_016006, NP_057090
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UniProt
- Q8WTS1
Target
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