Catalog No.
RHK61801
Species reactivity
Human respiratory syncytial virus A (strain rsb6256)
Host species
Mouse
Isotype
IgG2a
Clonality
Monoclonal
Target
CHD-7, Chromodomain-helicase-DNA-binding protein 7, ATP-dependent helicase CHD7, KIAA1416, CHD7
Concentration
1 mg/ml
Endotoxin level
Please contact with the lab for this information.
Purity
>95% as determined by SDS-PAGE.
Purification
Protein A/G purified from cell culture supernatant.
Accession
Q9P2D1
Applications
ELISA, IF, IP
Form
Liquid
Storage buffer
0.01M PBS, pH 7.4.
Stability and Storage
Use a manual defrost freezer and avoid repeated freeze-thaw cycles. Store at 4°C short term (1-2 weeks). Store at -20°C 12 months. Store at -80°C long term.
Clone ID
P004
A novel cardiomyopathy phenotype linked to a CHD7 missense variant., PMID:40461563
Epigenetic roles of chromatin remodeling complexes in bone biology and the pathogenesis of bone‑related disease (Review)., PMID:40444490
Chromatin modification abnormalities by CHD7 and KMT2C loss promote medulloblastoma progression., PMID:40393452
Multi-Omics Integration Analysis Revealed That miR-375-3p Is a Two-Sided Factor Regulating the Development and TUMORIGENESIS of Alzheimer's Disease., PMID:40332288
CHD7 binds distinct regions in the Sox11 locus to regulate neuronal differentiation., PMID:40236205
CHD7 binds to insulators during neuronal differentiation., PMID:40196636
Hyaluronidase 2 deficiency due to novel compound heterozygous variants in HYAL2: a case report of siblings with HYAL2 deficiency showing different clinical severity and literature review., PMID:40164710
Mutation of CHD7 impairs the output of neuroepithelium transition that is reversed by the inhibition of EZH2., PMID:40164694
[Clinical features of CHARGE syndrome in children]., PMID:40050103
Genetic and Clinical Predictors of Hearing Loss Among Patients with CHARGE Syndrome., PMID:40015694
Beyond CHD7 gene: unveiling genetic diversity in clinically suspected CHARGE syndrome., PMID:40000719
KMT2C Polymorphism in Familial Hypospadias., PMID:39812948
Systematic Ultrasound Evaluation of Olfactory Sulci in Fetuses with Congenital Heart Defects: A Clue for CHARGE Syndrome Diagnosis., PMID:39809240
Frontal lobe intra-axial schwannoma harboring a CHD7::VGLL3 fusion and heterozygous TSC2 p.F1510del mutation in a young child., PMID:39792305
VGLL fusions define a new class of intraparenchymal central nervous system schwannoma., PMID:39713960
Autosomally dominantly inherited isolated gonadotropin deficiency via maternal assisted reproduction due to SOX10 mutation., PMID:39680495
Let-7c-5p Targeting CHD7 Hinders Cervical Cancer Migration and Invasion by Regulating Cell Adhesion., PMID:39680330
Whole-genome sequencing analysis of Japanese autism spectrum disorder trios., PMID:39610113
Kallmann Syndrome: Functional Analysis of a CHD7 Missense Variant Shows Aberrant RNA Splicing., PMID:39596130
[CHARGE syndrome in a neonate]., PMID:39587755
Cooperative role of LSD1 and CHD7 in regulating differentiation of mouse embryonic stem cells., PMID:39557885
Deciphering HMGB1: Across a spectrum of DNA and nucleosome dynamics., PMID:39551968
Chromatin remodeller Chd7 is developmentally regulated in the neural crest by tissue-specific transcription factors., PMID:39418292
In Vivo CRISPR Screening Reveals CHD7 as a Positive Regulator of Short-lived Effector Cells., PMID:39373572
[Clinical phenotype and molecular genetic analysis of seven children with CHARGE syndrome]., PMID:39217482
Molecular characteristics and oncogenic role of CHD family genes: a pan-cancer analysis based on bioinformatic and biological analysis., PMID:39143142
Kismet/CHD7/CHD8 and Amyloid Precursor Protein-like Regulate Synaptic Levels of Rab11 at the Drosophila Neuromuscular Junction., PMID:39125997
[Clinical features and genetic analysis of a case with CHARGE syndrome due to variant of CHD7 gene]., PMID:39097280
Variety of genetic defects in GnRH and hypothalamic-pituitary signaling and development in normosmic patients with IHH., PMID:39010903
Kismet/CHD7/CHD8 affects gut microbiota, mechanics, and the gut-brain axis in Drosophila melanogaster., PMID:38902926
Human Genetics of Truncus Arteriosus., PMID:38884753
Human Genetics of Semilunar Valve and Aortic Arch Anomalies., PMID:38884747
Human Genetics of Tetralogy of Fallot and Double-Outlet Right Ventricle., PMID:38884738
Human Genetics of Ventricular Septal Defect., PMID:38884729
Human Genetics of Atrial Septal Defect., PMID:38884726
Epigenetics., PMID:38884720
Mutation spectrum of hearing loss patients in Northwest China: Identification of 20 novel variants., PMID:38860500
Genetic analysis of congenital unilateral renal agenesis in children based on next-generation sequencing., PMID:38849481
Deciphering potential causative factors for undiagnosed Waardenburg syndrome through multi-data integration., PMID:38844942
CHD7 Disorder-Not CHARGE Syndrome-Presenting as Isolated Cochleovestibular Dysfunction., PMID:38790272
IGF2BP2-modified circular RNA circCHD7 promotes endometrial cancer progression via stabilizing PDGFRB and activating JAK/STAT signaling pathway., PMID:38778089
Genetic diagnosis of endocrine disorders in Cyprus through the Cyprus Institute of Neurology and Genetics: an ENDO-ERN Reference Center., PMID:38637882
Fetal Phenotype of CHARGE Syndrome with a Molecular Confirmation: A Series of 13 Cases., PMID:38631314
Integrating trans-omics, cellular experiments and clinical validation to identify ILF2 as a diagnostic serum biomarker and therapeutic target in gastric cancer., PMID:38622522
Ocular manifestations of CHARGE syndrome in a pediatric cohort with genotype/phenotype analysis., PMID:38597178
Diagnosis challenges in CHARGE syndrome: A novel variant and clinical description., PMID:38545186
The CHD family chromatin remodeling enzyme, Kismet, promotes both clathrin-mediated and activity-dependent bulk endocytosis., PMID:38512854
CHD7 regulates craniofacial cartilage development via controlling HTR2B expression., PMID:38477756
The CHD Protein Kismet Restricts the Synaptic Localization of Cell Adhesion Molecules at the Drosophila Neuromuscular Junction., PMID:38474321
CHD7 and SOX2 act in a common gene regulatory network during mammalian semicircular canal and cochlear development., PMID:38408234
For research use only. Not for human or drug use.
