CHD7 Antibodies

AND CHD7 ELISA kits, CHD7 Proteins

Many biological assays use antibodies to detect CHD7, such as Western Blot (WB), ELISA, Flow Cytometry, Immunocytochemistry (IHC). These antibodies can be polyclonal or monoclonal, and react with CHD7 in Human, Mouse, Rat, and many other animal samples. Boster Bio use mainly mouse and rabbit to develop CHD7 antibodies...

We validate the specificity of these antibodies to CHD7 by testing them on tissues known to express CHD7 positively and negatively. Browse below to find the CHD7 antibody that suites your experiment. We have 2 of these antibodies and many publications and validation images.

If you cannot find antibodies that fit your needs, contact us for making custom antibodies. We have a full suite of custom antibody services covering from research to diagnostic and therapeutic applications.

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CHD7 Infographic by Boster Bio

All CHD7 Products

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Specificity

Applications

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Anti-Zebrafish CHD7 Antibody

1 Q&As

Zebrafish

$470
Cat # DZ01533
200 μl/vial

Anti-CHD7 Antibody

Human, Mouse

ELISA, IF, IHC-P, WB

$449
Cat # A01533
0.1 mg

CHD7 Overview

Facts about Chromodomain-helicase-DNA-binding protein 7.

Chromodomain-helicase-DNA-binding protein 7 (CHD7)

Probable transcription regulator. Maybe involved in the in 45S precursor rRNA production.

Gene Information

Human
Gene Name:	CHD7
Uniprot:	Q9P2D1
Entrez:	55636

Family

Belongs to:

SNF2/RAD54 helicase family

Alternative Names

ATP-dependent helicase CHD7; CHD7; CHD-7; chromodomain helicase DNA binding protein 7 isoform CRA_e; chromodomain helicase DNA binding protein 7; chromodomain-helicase-DNA-binding protein 7; EC 3.6.1; EC 3.6.4.12; FLJ20357; FLJ20361; IS3; KIAA1416KAL5

Molecular Weight

Mass (kDA):
335.927 kDA

Genomic Context


Human

Location:	8q12.2
Sequence:	8; NC_000008.11 (60678740..60868028)

Tissue Specificity

Widely expressed in fetal and adult tissues.

Subcellular Localizations

[Isoform 1]: Nucleus.; [Isoform 3]: Nucleus, nucleolus.

Diseases

Charge Syndrome
Congenital Ocular Coloboma (disorder)
Congenital Heart Defects
Atresia
Choanal Atresia
Congenital Abnormality
Complete Hearing Loss
Hypogonadotropic Hypogonadism
Hypogonadism
Hypoplasia
Kallmann Syndrome
Anosmia

Developmental Delay (disorder)
Haploinsufficiency
Growth Disorders
Developmental Disabilities
Digeorge Syndrome
Pituitary Diseases
Cytogenetic Abnormality

Interacting Proteins

PBRM1
SMARCC2

Pathways

Chromatin Remodeling
Pathogenesis
Atp-dependent Chromatin Remodeling
Neurogenesis
Cell Proliferation
Secretion
Ear Morphogenesis
Innervation
Inner Ear Morphogenesis
Stem Cell Proliferation
Segmentation
Methylation
Rna Interference

Cell Migration
Developmental Process
Pigmentation
Regulation Of Gene Expression
Root Morphogenesis
Tissue Development
Cell Motility

PTMs

Methylation

Reduction

Research Areas

Transcription Factors and Regulators

For details, visit:
bosterbio.com/bosterbio-gene-info-cards/CHD7

References

PMID: 20453063 by Batsukh T., et al. CHD8 interacts with CHD7, a protein which is mutated in CHARGE syndrome.

PMID: 22646239 by Kita Y., et al. Identification of CHD7S as a novel splicing variant of CHD7 with functions similar and antagonistic to those of the full-length CHD7L.