Bromodomain Adjacent To Zinc Finger Domain, 1B (BAZ1B) (Middle Region) Peptide
BAZ1B
Reactivité: Humain
Hôte: Synthetic
BP, WB
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- Antigène Tous les produits BAZ1B
- BAZ1B (Bromodomain Adjacent To Zinc Finger Domain, 1B (BAZ1B))
- Protein Region
- Middle Region
- Origine
- Humain
- Source
- Synthetic
- Application
- Blocking Peptide (BP), Western Blotting (WB)
- Attributs du produit
- This is a synthetic peptide designed for use in combination with anti-BAZ1B antibody (Catalog #: ARP39571_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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- Indications d'application
- 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.
- Conseil sur la manipulation
- Avoid repeated freeze-thaw cycles.
- Stock
- -20 °C
- Stockage commentaire
- For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
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- Antigène
- BAZ1B (Bromodomain Adjacent To Zinc Finger Domain, 1B (BAZ1B))
- Synonymes
- BAZ1B Peptide, wstf Peptide, wbscr9 Peptide, wbscr10 Peptide, LOC100220420 Peptide, WBSCR10 Peptide, WBSCR9 Peptide, WSTF Peptide, C87820 Peptide, Wbscr9 Peptide, fi60d02 Peptide, im:7137554 Peptide, wu:fi60d02 Peptide, bromodomain adjacent to zinc finger domain 1B Peptide, bromodomain adjacent to zinc finger domain, 1B Peptide, bromodomain adjacent to zinc finger domain 1B S homeolog Peptide, BAZ1B Peptide, baz1b Peptide, Baz1b Peptide, baz1b.S Peptide
- Sujet
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BAZ1B is a member of the bromodomain protein family. The bromodomain is a structural motif characteristic of proteins involved in chromatin-dependent regulation of transcription. This gene is deleted in Williams-Beuren syndrome, a developmental disorder caused by deletion of multiple genes at 7q11.23.This gene encodes a member of the bromodomain protein family. The bromodomain is a structural motif characteristic of proteins involved in chromatin-dependent regulation of transcription. This gene is deleted in Williams-Beuren syndrome, a developmental disorder caused by deletion of multiple genes at 7q11.23. 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: WBSCR10, WBSCR9, WSTF
Protein Interaction Partner: PCNA,MYO1C,PCNA,SMARCA1,SMARCA5,SMARCC2,SMARCE1,ACTL6A,ARID1A,BAZ1A,CDT1,CHAF1B,ESR1,SMARCA5,SMARCB1,SMARCC1,SMARCC2,SMARCD1,SMARCE1,SUPT16H,TOP2B,TRNAG1,VDR
Protein Size: 1483 - Poids moléculaire
- 171 kDa
- ID gène
- 9031
- NCBI Accession
- NM_032408, NP_115784
- UniProt
- Q9UIG0
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