BAZ1B anticorps (Middle Region)
Aperçu rapide pour BAZ1B anticorps (Middle Region) (ABIN2781194)
Antigène
Voir toutes BAZ1B AnticorpsReactivité
Hôte
Clonalité
Conjugué
Application
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Épitope
- Middle Region
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Fonction
- BAZ1B Antibody - middle region
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Séquence
- EQCLVALLHK HLPGHPYVRR KRKKFPDRLA EDEGDSEPEA VGQSRGRRQK
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Homologie
- Cow: 93%, Dog: 86%, Guinea Pig: 86%, Horse: 86%, Human: 100%, Mouse: 79%, Pig: 93%, Rat: 79%
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Attributs du produit
- This is a rabbit polyclonal antibody against BAZ1B. It was validated on Western Blot using a cell lysate as a positive control.
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Purification
- Affinity Purified
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Immunogène
- The immunogen is a synthetic peptide directed towards the middle region of human BAZ1B
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Indications d'application
- Optimal working dilution should be determined by the investigator.
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Commentaires
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We also sell a specific blocking peptide that can be used in combination with this antibody. You can find the blocking peptide under AAP39571-100UG
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Restrictions
- For Research Use only
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Format
- Liquid
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Concentration
- 0.5 mg/mL
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Buffer
- Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.
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Agent conservateur
- Sodium azide
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Précaution d'utilisation
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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Conseil sur la manipulation
- prevent freeze-thaw cycles
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Stock
- 4 °C,-20 °C
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Stockage commentaire
- For short term use, store at 2-8C up to 1 week. For long term storage, store at -20 °C in small aliquots to prevent freeze-thaw cycles.
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- BAZ1B (Bromodomain Adjacent To Zinc Finger Domain, 1B (BAZ1B))
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Autre désignation
- BAZ1B
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Sujet
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Background Information: 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.
Gene Name: Bromodomain adjacent to zinc finger domain, 1B
Alternative Symbols: WSTF, WBSCR9, WBSCR10
Protein Name: Tyrosine-protein kinase BAZ1B
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Poids moléculaire
- 171kDa
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ID gène
- 9031
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NCBI Accession
- NP_115784
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UniProt
- Q9UIG0
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Pathways
- Nuclear Hormone Receptor Binding, Chromatin Binding
Antigène
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