BRD9 Antibody (N-term)
Affinity Purified Rabbit Polyclonal Antibody (Pab)
- SPECIFICATION
- CITATIONS
- PROTOCOLS
- BACKGROUND
Application
| IHC-P, WB, E |
---|---|
Primary Accession | Q9H8M2 |
Other Accession | NP_001009877.2 |
Reactivity | Human, Mouse |
Host | Rabbit |
Clonality | Polyclonal |
Isotype | Rabbit IgG |
Calculated MW | 67000 Da |
Antigen Region | 3-29 aa |
Gene ID | 65980 |
---|---|
Other Names | Bromodomain-containing protein 9, Rhabdomyosarcoma antigen MU-RMS-408, BRD9 |
Target/Specificity | This BRD9 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 3-29 amino acids from the N-terminal region of human BRD9. |
Dilution | WB~~1:1000 IHC-P~~1:100 |
Format | Purified polyclonal antibody supplied in PBS with 0.09% (W/V) sodium azide. This antibody is purified through a protein A column, followed by peptide affinity purification. |
Storage | Maintain refrigerated at 2-8°C for up to 2 weeks. For long term storage store at -20°C in small aliquots to prevent freeze-thaw cycles. |
Precautions | BRD9 Antibody (N-term) is for research use only and not for use in diagnostic or therapeutic procedures. |
Name | BRD9 |
---|---|
Function | Plays a role in chromatin remodeling and regulation of transcription (PubMed:22464331, PubMed:26365797). Acts as a chromatin reader that recognizes and binds acylated histones: binds histones that are acetylated and/or butyrylated (PubMed:26365797). Component of SWI/SNF chromatin remodeling subcomplex GBAF that carries out key enzymatic activities, changing chromatin structure by altering DNA- histone contacts within a nucleosome in an ATP-dependent manner (PubMed:29374058). Orchestrates also the RAD51-RAD54 complex formation and thereby plays a role in homologous recombination (HR) (PubMed:32457312). |
Cellular Location | Nucleus. |
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Provided below are standard protocols that you may find useful for product applications.
Background
BRD9 is a bromodomain containing protein, which are known to bind to acetylated lysine residues.
References
Rose, J.E., et al. Mol. Med. 16 (7-8), 247-253 (2010) :
Scotto, L., et al. Mol. Cancer 7, 58 (2008) :
Clark, H.F., et al. Genome Res. 13(10):2265-2270(2003)
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