Myosin VI (MYO6) (C-Term) Peptide
MYO6
Reactivité: Humain
Hôte: Synthetic
BP, WB
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- Antigène Tous les produits Myosin VI (MYO6)
- Myosin VI (MYO6)
- Protein Region
- C-Term
- Origine
- Humain
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Source
- Synthetic
- Application
- Blocking Peptide (BP), Western Blotting (WB)
- Séquence
- SPQQNPAAQI PARQREIEMN RQQRFFRIPF IRPADQYKDP QSKKKGWWYA
- Attributs du produit
- This is a synthetic peptide designed for use in combination with anti- MYO6 Antibody. 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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- Indications d'application
- Optimal working dilution should be determined by the investigator.
- 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.
- Stock
- -20 °C
- Stockage commentaire
- For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
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- Antigène
- Myosin VI (MYO6)
- Synonymes
- 95F Peptide, 95F MHC Peptide, CG5695 Peptide, Dm 95F Peptide, Dm95F Peptide, Dmel\\CG5695 Peptide, Dro95F Peptide, JAG Peptide, Jaguar Peptide, Jar Peptide, M6 Peptide, MHC95F Peptide, MYOVI Peptide, Mhc95F Peptide, MyoVI Peptide, Myosin VI Peptide, jag Peptide, ms(3)06746 Peptide, myosins VI Peptide, DFNA22 Peptide, DFNB37 Peptide, BC029719 Peptide, Tlc Peptide, sv Peptide, RGD1560646 Peptide, CMY6 Peptide, jaguar Peptide, myosin VI Peptide, jar Peptide, LOC373230 Peptide, MYO6 Peptide, myo6 Peptide, Myo6 Peptide
- Sujet
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This gene encodes a reverse-direction motor protein that moves toward the minus end of actin filaments and plays a role in intracellular vesicle and organelle transport. The protein consists of a motor domain containing an ATP- and an actin-binding site and a globular tail which interacts with other proteins. This protein maintains the structural integrity of inner ear hair cells and mutations in this gene cause non-syndromic autosomal dominant and recessive hearing loss. Alternative splicing results in multiple transcript variants encoding distinct isoforms.
Alias Symbols: DFNA22, DFNB37
Protein Size: 1294 - ID gène
- 4646
- NCBI Accession
- NM_001300899, NP_001287828
- UniProt
- Q9UM54
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