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Chromodomain Helicase DNA Binding Protein 7 (CHD7) ELISA Kits

CHD7 encodes a protein that contains several helicase family domains. Additionally we are shipping CHD7 Antibodies (42) and many more products for this protein.

list all ELISA KIts Gene Name GeneID UniProt
CHD7 55636 Q9P2D1
CHD7 320790 A2AJK6
CHD7 312974  
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Top CHD7 ELISA Kits at antibodies-online.com

Showing 3 out of 3 products:

Catalog No. Reactivity Sensitivity Range Quantity Supplier Delivery Price Details
Mouse
96 Tests Log in to see 16 to 21 Days
$999.43
Details
Rat
96 Tests Log in to see 16 to 21 Days
$999.43
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Human
96 Tests Log in to see 16 to 21 Days
$999.43
Details

More ELISA Kits for CHD7 Interaction Partners

Xenopus laevis Chromodomain Helicase DNA Binding Protein 7 (CHD7) interaction partners

  1. evolutionarily conserved role for CHD7 in orchestrating neural crest gene expression programs

Zebrafish Chromodomain Helicase DNA Binding Protein 7 (CHD7) interaction partners

  1. knockdown of the jumonji (show JARID2 ELISA Kits) domain-containing histone demethylase (show MBD2 ELISA Kits) fbxl10 (show KDM2B ELISA Kits)/kdm2bb, a repressor of ribosomal RNA genes, rescues cell proliferation and cartilage defects in chd7 morphant embryos and can lead to complete rescue of the CHARGE syndrome phenotype.

  2. Chd7 is required for the organization of the neural retina in zebrafish.

  3. Data show that Chd7 deficiency leads to asymmetric segmentation of the presomitic mesoderm (PSM), and results in the loss of asymmetric expression of spaw in the lateral plate mesoderm, which is consistent with more general laterality defects.

Human Chromodomain Helicase DNA Binding Protein 7 (CHD7) interaction partners

  1. Pathogenic CHD7 variants are associated with CHARGE syndrome.

  2. Two mutations of CHD7 were identified including a novel splice-site mutation (c.2443-2A>G) and a previously known frameshift mutation (c.2504_2508delATCTT).

  3. CHD7 mutations and CHARGE syndrome (Review)

  4. Here, we review recent work aimed at understanding the mechanism of CHD7 function in normal and pathological states, highlighting results from biochemical and in vivo studies.

  5. Like KMT2D (show MLL2 ELISA Kits), CHD7 interacts with members of the WAR complex, namely WDR5 (show WDR5 ELISA Kits), ASH2L and RbBP5 (show RBBP5 ELISA Kits). We therefore propose that CHD7 and KMT2D (show MLL2 ELISA Kits) function in the same chromatin modification machinery.

  6. CHARGE syndrome due to deletion of region upstream of CHD7 gene START codon.

  7. These data provide additional evidence that CHD7 mutations are a significant cause of semicircular canal atresia in children with full or partial CHARGE syndrome.

  8. CHD7 mutations are not a major cause of atrioventricular septal and conotruncal heart defects.

  9. Functionally compromised CHD7 missense alleles contribute to the pathogenesis of both the anosmic and normosmic forms of Isolated gonadotropin-releasing hormone deficiency.

  10. Two new intronic CHD7 mutations are associated with CHARGE syndrome phenotype.

Mouse (Murine) Chromodomain Helicase DNA Binding Protein 7 (CHD7) interaction partners

  1. Chd7 (show CHD3 ELISA Kits) mutant mice are models for determining the molecular etiology of ocular defects in CHARGE syndrome.

  2. This work reveals the importance of CHD7 (show CHD3 ELISA Kits) in the cardiogenic mesoderm for multiple processes during cardiovascular development.

  3. Findings directly link CHD7 (show CHD3 ELISA Kits) to pathways involved in NSC quiescence and identify the first chromatin-remodeling factor (show ASH1L ELISA Kits) with a role in NSC quiescence and maintenance.

  4. Conditional deletion of Chd7 (show CHD3 ELISA Kits) in ectodermal and endodermal derivatives or migrating neural crest cells results in varied and severe craniofacial defects.

  5. CHD7 (show CHD3 ELISA Kits) gene mutation is associated with CHARGE syndrome.

  6. Findings demonstrate critical, cooperative roles for Retinoic Acid (RA) and CHD7 (show CHD3 ELISA Kits) in subventricular zone neural stem cell function and inner ear development, suggesting that altered RA signaling may be an effective method for treating Chd7 (show CHD3 ELISA Kits) deficiency.

  7. Chd7 (show CHD3 ELISA Kits) may have critical selector gene functions during inner ear morphogenesis.

  8. CHD7 (show CHD3 ELISA Kits) may directly regulate Bmp4 (show BMP4 ELISA Kits) expression by binding with an enhancer element downstream of the Bmp4 (show BMP4 ELISA Kits) locus.

  9. Chd7 (show CHD3 ELISA Kits)(Gt)(/+) mouse model of CHARGE syndrome demonstrates combined conductive and sensorineural hearing loss, correlating with changes in both middle and inner ears.

  10. characterize gene regulation by Sox2 (show SOX2 ELISA Kits) in neural stem cells. We

CHD7 Antigen Profile

Antigen Summary

This gene encodes a protein that contains several helicase family domains. Mutations in this gene have been found in some patients with the CHARGE syndrome.

Gene names and symbols associated with CHD7

  • chromodomain helicase DNA binding protein 7 (chd7) antibody
  • chromodomain helicase DNA binding protein 7 (CHD7) antibody
  • chromodomain helicase DNA binding protein 7 (Chd7) antibody
  • A730019I05Rik antibody
  • CHD7 antibody
  • Cycn antibody
  • Cyn antibody
  • Dz antibody
  • Edy antibody
  • fd19h06 antibody
  • Flo antibody
  • GENA 47 antibody
  • Gena 52 antibody
  • GENA 60 antibody
  • HH5 antibody
  • IS3 antibody
  • KAL5 antibody
  • Lda antibody
  • metis antibody
  • Mt antibody
  • Obt antibody
  • si:ch211-197o6.2 antibody
  • Todo antibody
  • WBE1 antibody
  • Whi antibody
  • wu:cegs2051 antibody
  • wu:fb37f10 antibody
  • wu:fb39h04 antibody
  • wu:fd19h06 antibody

Protein level used designations for CHD7

chromodomain helicase DNA binding protein 7 , fb37f10 , fb39h04 , chromodomain-helicase-DNA-binding protein 7-like , ATP-dependent helicase CHD7 , chromodomain helicase DNA binding protein 7 isoform CRA_e , chromodomain-helicase-DNA-binding protein 7 , CHD-7 , chromodomain helicase DNA-binding protein 7

GENE ID SPECIES
443577 Xenopus laevis
464198 Pan troglodytes
486968 Canis lupus familiaris
533175 Bos taurus
569471 Danio rerio
100339550 Oryctolagus cuniculus
100379668 Xenopus (Silurana) tropicalis
100461260 Pongo abelii
100479808 Ailuropoda melanoleuca
100580875 Nomascus leucogenys
55636 Homo sapiens
320790 Mus musculus
312974 Rattus norvegicus
421140 Gallus gallus
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