Tu Translation Elongation Factor, Mitochondrial (Tufm) (Middle Region) Peptide
Tufm
Reactivity: Human
Host: Synthetic
BP, WB
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- Target See all TUFM (Tufm) products
- TUFM (Tufm) (Tu Translation Elongation Factor, Mitochondrial (Tufm))
- Protein Region
- Middle Region
- Origin
- Human
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Source
- Synthetic
- Application
- Blocking Peptide (BP), Western Blotting (WB)
- Characteristics
- This is a synthetic peptide designed for use in combination with anti-TUFM antibody (Catalog #: ARP58546_P050). 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.
- Purification
- Purified
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- Application Notes
- Each Investigator should determine their own optimal working dilution for specific applications.
- Restrictions
- For Research Use only
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- Format
- Lyophilized
- Reconstitution
- Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.
- Concentration
- 1 mg/mL
- Buffer
- Final peptide concentration is 1 mg/mL in PBS.
- Handling Advice
- Avoid repeated freeze-thaw cycles.
- Storage
- -20 °C
- Storage Comment
- For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
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- Target
- TUFM (Tufm) (Tu Translation Elongation Factor, Mitochondrial (Tufm))
- Synonyms
- TUFM Peptide, D250 Peptide, fi06f04 Peptide, wu:fi06f04 Peptide, zgc:110766 Peptide, COXPD4 Peptide, EF-TuMT Peptide, EFTU Peptide, P43 Peptide, 2300002G02Rik Peptide, C76308 Peptide, C76389 Peptide, Tu translation elongation factor, mitochondrial Peptide, TUFM Peptide, tufm Peptide, Tufm Peptide
- Background
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TUFM is a protein which participates in protein translation in mitochondria. Mutations in this gene have been associated with combined oxidative phosphorylation deficiency resulting in lactic acidosis and fatal encephalopathy. This gene encodes a protein which participates in protein translation in mitochondria. Mutations in this gene have been associated with combined oxidative phosphorylation deficiency resulting in lactic acidosis and fatal encephalopathy. A pseudogene has been identified on chromosome 17. Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Entrez Gene record to access additional publications.
Alias Symbols: COXPD4, EF-TuMT, EFTU, P43
Protein Interaction Partner: ATP6V1A,MYH9,SGK1
Protein Size: 455 - Molecular Weight
- 50 kDa
- Gene ID
- 7284
- NCBI Accession
- NM_003321, NP_003312
- UniProt
- P49411
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