CHD5 Antibody

Code CSB-PA265689
Size US$297
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  • Immunohistochemical analysis of paraffin-embedded Human tonsil cancer tissue using at dilution 1/40.
  • Immunohistochemical analysis of paraffin-embedded Human liver cancer tissue using at dilution 1/40.
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Product Details

Full Product Name
Rabbit anti-Homo sapiens (Human) CHD5 Polyclonal antibody
Uniprot No.
Target Names
CHD5
Alternative Names
ATP-dependent helicase CHD5 antibody; CHD 5 antibody; CHD-5 antibody; CHD5 antibody; CHD5_HUMAN antibody; Chromodomain-helicase-DNA-binding protein 5 antibody; DKFZp434N231 antibody; KIAA0444 antibody; RP1-233K16.2 antibody
Raised in
Rabbit
Species Reactivity
Human,Mouse,Rat
Immunogen
Synthetic peptide corresponding to residues near the C terminal of Human Cadherin 5, type 2 (vascular endothelium)
Immunogen Species
Homo sapiens (Human)
Clonality
Polyclonal
Purification Method
Antigen Affinity Purified
Concentration
It differs from different batches. Please contact us to confirm it.
Form
Rabbit IgG in pH7.3 PBS, 0.05% NaN3, 50% Glycerol.
Tested Applications
ELISA,IHC
Recommended Dilution
Application Recommended Dilution
IHC 1:50-1:100
Troubleshooting and FAQs
Storage
Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
Lead Time
Basically, we can dispatch the products out in 1-3 working days after receiving your orders. Delivery time maybe differs from different purchasing way or location, please kindly consult your local distributors for specific delivery time.

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Target Background

Function
Chromatin-remodeling protein that binds DNA through histones and regulates gene transcription. May specifically recognize and bind trimethylated 'Lys-27' (H3K27me3) and non-methylated 'Lys-4' of histone H3. Plays a role in the development of the nervous system by activating the expression of genes promoting neuron terminal differentiation. In parallel, it may also positively regulate the trimethylation of histone H3 at 'Lys-27' thereby specifically repressing genes that promote the differentiation into non-neuronal cell lineages. Tumor suppressor, it regulates the expression of genes involved in cell proliferation and differentiation. Downstream activated genes may include CDKN2A that positively regulates the p53/TP53 pathway, which in turn, prevents cell proliferation. In spermatogenesis, it probably regulates histone hyperacetylation and the replacement of histones by transition proteins in chromatin, a crucial step in the condensation of spermatid chromatin and the production of functional spermatozoa.
Gene References into Functions
  1. CHD5 was identified as a direct target of miR-454. CHD5 was downregulated in GC tissues/cell lines and the expresssion of CHD5 inversely correlated with the level of miR-454 in GC tissues. Taken together, these observations indicate that HDAC3 is associated with GC cell growth via the miR-454-mediated targeting of CHD5. PMID: 29115379
  2. Data show that chromodomain helicase DNA binding protein 5 (CHD5) acted as a functional tumor suppressor and was frequently silenced by promoter CpG methylation in renal cell carcinoma (RCC). PMID: 26943038
  3. CHD5 may act as a tumor suppressor gene in NSCLC. PMID: 28400267
  4. Authors identified the CHD5 as a direct target of miR-454. CHD5 was downregulated in HCC tissues and cell lines and the expression level of CHD5 was inversely correlated with the expression of miR-454 in HCC tissues. PMID: 26287602
  5. Data show a mutual suppression regulation between chromodomain helicase DNA binding protein 5 (CHD5) and enhancer of zeste homolog 2 (EZH2, which may provide new insights into their potential therapeutic significance for hepatocellular carcinoma (HCC). PMID: 26517514
  6. CHD5 methylation of rectal cancer has a great effect in influencing its clinical and pathological features. PMID: 26753653
  7. Study shows that CHD5 is a Nucleosome remodeling and deacetylase complex-associated transcriptional repressor and identifies WEE1 as one of the CHD5-regulated genes that may link CHD5 to tumor suppression. PMID: 25247294
  8. Low CHD5 expression activates the DNA damage response and predicts poor outcome in patients undergoing adjuvant therapy for resected pancreatic cancer. PMID: 24276239
  9. CHD5 is a potential tumour suppressor gene epigenetically silenced in hepatocellular carcinoma. PMID: 24529164
  10. The tumor suppressor chromodomain helicase DNA-binding protein 5 (CHD5) remodels nucleosomes by unwrapping. PMID: 24923445
  11. repression of CHD5 gene expression in human leukemia is mediated in part by DNA methylation of its promoter. PMID: 24454811
  12. CHD5 activity is regulated by DNA methylation and repressive histone modifications. CHD5 likely acts as a tumor-suppressor gene in early colorectal carcinogenesis. PMID: 24243398
  13. CHD5 might act as a tumor suppressor in glioma PMID: 23707602
  14. These findings provide insights into the regulatory role of CHD5 during neurogenesis and suggest how inactivation of this candidate tumor suppressor might contribute to neuroblastoma. PMID: 23948251
  15. Decreased expression of chromodomain helicase DNA-binding protein 5 is associated with primary gallbladder carcinoma PMID: 22855185
  16. CHD% protein mediates the p53-dependent senescence program triggered by decreased JMJD2A levels. PMID: 23168260
  17. study concludes that down-regulation of CHD5, mediated at least in part by promoter methylation, contributes to the development and progression of human breast cancer PMID: 22569290
  18. In this Caucasian population, endometriosis seems to be associated with the tumor-suppressor gene CHD5. Our findings support recent data, suggesting that the 1p36 region plays an important role in endometrios. PMID: 22910690
  19. CHD5 is a potential tumor suppressor gene that is inactivated via an epigenetic mechanism in lung cancer. PMID: 22186629
  20. Studies identified three genes, CHD5, PAFAH1B1, and NME1, strongly associated with patient outcome. PMID: 22328561
  21. We conclude that (i) somatically acquired CHD5 mutations are rare in primary NBs, so inactivation probably occurs by deletion and epigenetic silencing. PMID: 22294723
  22. the association of between miR-211-regulated CHD5 expression and CHD5 function in colorectal tumorigenesis PMID: 22235338
  23. CHD5 is downregulated in a certain number of ovarian cancers and appears to be an adverse predictor candidate of ovarian cancer disease-free and total survival. PMID: 21860208
  24. data suggest that CHD5 is a tumor suppressor gene that is epigenetically downregulated in laryngeal squamous cell carcinoma. PMID: 21636313
  25. As only one of the 47 families studied has the CHD5 rs7513548 SNP variant, it appears to be a rare event and further screening of melanoma families is required to confirm whether or not CHD5 is involved in melanoma pathogenesis. PMID: 21250965
  26. Data show a strong association of CHD5 expression with favorable prognostic variables (age at diagnosis <12 months, low clinical stage, and favorable histology), overall survival and event-free survival. PMID: 20950435
  27. CHD5 is a tumor suppressor gene epigenetically down-regulated in gastric cancer PMID: 19840376
  28. CDH5 may play a role in the development of the nervous system, and it may also play a role in the pathogenesis of neural tumors. PMID: 12592387
  29. Study demonstrates that Chd5 functions as a tumor suppressor in vivo and implicates deletion of CHD5 in human cancer. PMID: 17289567
  30. A recent functional study identified chromodomain helicase DNA-binding protein 5 (CHD5) as a novel tumor suppressor mapping to 1p36. [REVIEW] PMID: 18413720
  31. CHD5 is the strongest candidate tumor suppressor gene that is deleted from 1p36.31 in neuroblastomas, and inactivation of the second allele may occur by an epigenetic mechanism. PMID: 18577749
  32. the DNA methylation profiles of CHD family members (CHD1-9) in different tumor types. PMID: 18698156
  33. study demonstrated the existence of somatic mutations and methylation of CHD5 in primary epithelial ovarian cancers; CHD5 may play a role as a tumor suppressor gene in ovarian cancer PMID: 18953434

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Involvement in disease
Defects in CHD5 may be a cause of the development of cancers from epithelial, neural and hematopoietic origin. CHD5 is one of the missing genes in the del(1p36), a deletion which is extremely common in this type of cancers. A decrease of its expression, results in increased susceptibility of cells to Ras-mediated transformation in vitro and in vivo (PubMed:17289567).
Subcellular Location
Nucleus.
Protein Families
SNF2/RAD54 helicase family
Tissue Specificity
Preferentially expressed in total brain, fetal brain, and cerebellum. It is also moderately expressed in the adrenal gland and detected in testis.
Database Links

HGNC: 16816

OMIM: 610771

KEGG: hsa:26038

STRING: 9606.ENSP00000262450

UniGene: Hs.522898

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