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          • Primary Antibodies ›
          • BAZ1B Antibodies

          Abnova

          BAZ1B Monoclonal Antibody (5E9)

          View all (16) BAZ1B antibodies
          Datasheet
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          Datasheet
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          Cite BAZ1B Monoclonal Antibody (5E9)

          Product Details

          H00009031-M01A

          Applications
          Tested Dilution
          Publications

          ELISA (ELISA)

          10 µg/mL
          -
          Product Specifications

          Species Reactivity

          Human

          Host/Isotype

          Mouse / IgG2a, kappa

          Class

          Monoclonal

          Type

          Antibody

          Clone

          5E9

          Immunogen

          BAZ1B (NP_075381, 1384 a.a. approximately 1483 a.a) partial recombinant protein with GST tag. MW of the GST tag alone is 26 KDa.
          View immunogen

          Conjugate

          Unconjugated Unconjugated Unconjugated

          Form

          Liquid

          Concentration

          See Label

          Storage buffer

          ascites

          Contains

          no preservative

          Storage conditions

          -20°C, Avoid Freeze/Thaw Cycles

          Shipping conditions

          Ambient (domestic); Wet ice (international)

          Product Specific Information

          Sequence of this protein is as follows: MDFQTVQNKC SCGSYRSVQE FLTDMKQVFT NAEVYNCRGS HVLSCMVKTE QCLVALLHKH LPGHPYVRRK RKKFPDRLAE DEGDSEPEAV GQSRGRRQKK

          Target 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.

          For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.

          References (0)

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          Cite this product

          Bioinformatics

          Protein Aliases: Bromodomain adjacent to zinc finger domain protein 1B; bromodomain adjacent to zinc finger domain, 1B; hWALp2; transcription factor WSTF; Tyrosine-protein kinase BAZ1B; Williams syndrome transcription factor; Williams-Beuren syndrome chromosomal region 10 protein; Williams-Beuren syndrome chromosomal region 9 protein

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          Gene Aliases: BAZ1B; WBSC10; WBSCR10; WBSCR9; WSTF

          View more View less

          UniProt ID: (Human) Q9UIG0

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          Entrez Gene ID: (Human) 9031

          View more View less

          Function(s)
          chromatin binding protein tyrosine kinase activity non-membrane spanning protein tyrosine kinase activity protein binding ATP binding zinc ion binding histone kinase activity lysine-acetylated histone binding vitamin D receptor activator activity
          Process(es)
          heart morphogenesis double-strand break repair chromatin assembly or disassembly transcription, DNA-templated regulation of transcription, DNA-templated cellular response to DNA damage stimulus histone phosphorylation peptidyl-tyrosine phosphorylation positive regulation of gene expression, epigenetic chromatin-mediated maintenance of transcription positive regulation of receptor activity
          It has to be done as per old AB suggested Products section.
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          If an Invitrogen™ antibody doesn't perform as described on our website or datasheet,we'll replace the product at no cost to you, or provide you with a credit for a future purchase.*

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