BAZ1B antibody (Middle Region)
Quick Overview for BAZ1B antibody (Middle Region) (ABIN2781194)
Target
See all BAZ1B AntibodiesReactivity
Host
Clonality
Conjugate
Application
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Binding Specificity
- Middle Region
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Sequence
- EQCLVALLHK HLPGHPYVRR KRKKFPDRLA EDEGDSEPEA VGQSRGRRQK
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Predicted Reactivity
- Cow: 93%, Dog: 86%, Guinea Pig: 86%, Horse: 86%, Human: 100%, Mouse: 79%, Pig: 93%, Rat: 79%
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Characteristics
- 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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Immunogen
- The immunogen is a synthetic peptide directed towards the middle region of human BAZ1B
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Application Notes
- Optimal working dilutions should be determined experimentally by the investigator.
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Comment
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Antigen size: 1483 AA
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Restrictions
- For Research Use only
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Format
- Liquid
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Concentration
- Lot specific
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Buffer
- Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.
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Preservative
- Sodium azide
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Precaution of Use
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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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 short term use, store at 2-8°C 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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Alternative Name
- BAZ1B
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Background
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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: VDR, TOP2B, SMARCC2, SMARCC1, HIST1H3A, UBC, EED, RNF2, NR4A2, LMNA, HDAC11, WHSC1, MBD3, SRRM2, SMARCA5, SMARCD2, SMARCA4, SIRT7, SUMO2, HDGF, SUMO1, tat, PCNA, SIN3A, NCOR1, HIST1H4A, HIST2H2BE, HIST2H2AC, TCF3, HDAC2, DEK, RHD, MYO1C, MYBBP1A, SF3B1, E
Protein Size: 1483 -
Molecular Weight
- 171 kDa
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Gene ID
- 9031
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NCBI Accession
- NM_032408, NP_115784
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UniProt
- Q9UIG0
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Pathways
- Nuclear Hormone Receptor Binding, Chromatin Binding
Target
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