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BCOR Antibody (PACO07999)

SKU:
PACO07999
Product Type:
Antibody
Reactivity:
Human
Mouse
Rat
Host Species:
Rabbit
Isotype:
IgG
Applications:
ELISA
WB
Antibody Type:
Polyclonal Antibody
Conjugation:
Unconjugated
$551
Frequently bought together:

Description

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BCOR Antibody (PACO07999)

The BCOR Polyclonal Antibody (PACO07999) is a crucial tool for research involving BCOR, a transcriptional corepressor involved in various cellular processes, including gene silencing and differentiation. This antibody, produced in rabbits, is highly specific to human samples and has been validated for use in applications such as Western blot and immunohistochemistry.BCOR is known to play a significant role in development and disease, with mutations in the gene associated with various cancers and developmental disorders. By targeting BCOR with this antibody, researchers can study its expression and function in different cell types, providing valuable insights into its role in normal cellular processes and disease pathology.

With its high reactivity and specificity, the BCOR Polyclonal Antibody is an essential tool for researchers in the fields of cancer biology, developmental biology, and molecular genetics. By further understanding the mechanisms involving BCOR, new therapeutic strategies may be developed for diseases associated with BCOR dysregulation.

Antibody Name:BCOR Antibody (PACO07999)
Antibody SKU:PACO07999
Size:50ul
Host Species:Rabbit
Tested Applications:ELISA, WB
Recommended Dilutions:
Species Reactivity:Human, Mouse, Rat
Immunogen:Human BCOR
Form:Liquid
Storage Buffer:PBS with 0.1% Sodium Azide, 50% Glycerol, pH 7.3. -20°C, Avoid freeze / thaw cycles.
Purification Method:Antigen Affinity Purified
Clonality:Polyclonal
Isotype:IgG
Conjugate:Non-conjugated
Synonyms:BCL6 co-repressor;BCOR;ANOP2;FLJ20285;FLJ38041;KIAA1575;MAA2;MCOPS2;MGC131961;MGC71031 ;
UniProt Protein Function:BCOR: Transcriptional corepressor. May specifically inhibit gene expression when recruited to promoter regions by sequence specific DNA-binding proteins such as BCL6 and MLLT3. This repression may be mediated at least in part by histone deacetylase activities which can associate with this corepressor. Involved in the repression of TFAP2A; impairs binding of BCL6 and KDM2B to TFAP2A promoter regions. Via repression of TFAP2A acts as a negative regulator of osteo-dentiogenic capacity in adult stem cells; the function implies inhibition of methylation on histone H3 'Lys-4' (H3K4me3) and 'Lys-36' (H3K36me2). Defects in BCOR are the cause of microphthalmia syndromic type 2 (MCOPS2). Microphthalmia is a clinically heterogeneous disorder of eye formation, ranging from small size of a single eye to complete bilateral absence of ocular tissues (anophthalmia). In many cases, microphthalmia/anophthalmia occurs in association with syndromes that include non-ocular abnormalities. MCOPS2 is a very rare multiple congenital anomaly syndrome characterized by eye anomalies (congenital cataract, microphthalmia, or secondary glaucoma), facial abnormalities (long narrow face, high nasal bridge, pointed nose with cartilages separated at the tip, cleft palate, or submucous cleft palate), cardiac anomalies (atrial septal defect, ventricular septal defect, or floppy mitral valve) and dental abnormalities (canine radiculomegaly, delayed dentition, oligodontia, persistent primary teeth, or variable root length). Belongs to the BCOR family. 4 isoforms of the human protein are produced by alternative splicing.
UniProt Protein Details:

Protein type:Transcription, coactivator/corepressor

Chromosomal Location of Human Ortholog: Xp11.4

Cellular Component: mitochondrion; nucleus; PcG protein complex

Molecular Function:heat shock protein binding; histone deacetylase binding; protein binding; transcription corepressor activity; transcription factor binding; ubiquitin-protein ligase activity

Biological Process: heart development; negative regulation of bone mineralization; negative regulation of histone H3-K36 methylation; negative regulation of histone H3-K4 methylation; negative regulation of transcription from RNA polymerase II promoter; negative regulation of transcription, DNA-dependent; odontogenesis; palate development; specification of axis polarity

Disease: Microphthalmia, Syndromic 1; Microphthalmia, Syndromic 2

NCBI Summary:The protein encoded by this gene was identified as an interacting corepressor of BCL6, a POZ/zinc finger transcription repressor that is required for germinal center formation and may influence apoptosis. This protein selectively interacts with the POZ domain of BCL6, but not with eight other POZ proteins. Specific class I and II histone deacetylases (HDACs) have been shown to interact with this protein, which suggests a possible link between the two classes of HDACs. Several transcript variants encoding different isoforms have been found for this gene. A pseudogene of this gene is found on chromosome Y.[provided by RefSeq, Jun 2010]
UniProt Code:Q6W2J9
NCBI GenInfo Identifier:57012588
NCBI Gene ID:54880
NCBI Accession:Q6W2J9.1
UniProt Secondary Accession:Q6W2J9,Q29RF6, Q6P4B6, Q7Z2K7, Q8TEB4, Q96DB3, Q9H232 Q9H233, Q9HCJ7, Q9NXF2, D3DWB3, D3DWB4,
UniProt Related Accession:Q6W2J9
Molecular Weight:186,235 Da
NCBI Full Name:BCL-6 corepressor
NCBI Synonym Full Names:BCL6 corepressor
NCBI Official Symbol:BCOR  
NCBI Official Synonym Symbols:MAA2; ANOP2; MCOPS2  
NCBI Protein Information:BCL-6 corepressor
UniProt Protein Name:BCL-6 corepressor
Protein Family:BCL-6 corepressor
UniProt Gene Name:BCOR  
UniProt Entry Name:BCOR_HUMAN

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