CHD4 Antikörper (N-Term)

Produktnummer ABIN7879585

Der Kaninchen Polyklonal anti-CHD4 Antikörper (ABIN7879585) detektiert spezifisch CHD4 in WB und FACS. Dieser Antikörper reagiert spezifisch mit Proben aus Human.

Kurzübersicht für CHD4 Antikörper (N-Term) (ABIN7879585)

Target: CHD4 (Chromodomain Helicase DNA Binding Protein 4 (CHD4))

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser CHD4 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB), Flow Cytometry (FACS)

Produktdetails anti-CHD4 Antikörper

Bindungsspezifität: N-Term

Verwendungszweck: CHD4 Antibody / Chromodomain-helicase-DNA-binding protein 4 / Mi2-beta

Aufreinigung: Immunogen affinity purified

Immunogen: A synthetic peptide corresponding to a sequence at the N-terminus of human CHD4 was used as the immunogen for the CHD4 antibody.

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: Optimal dilution of the CHD4 antibody should be determined by the researcher.

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Lyophilized

Rekonstitution: Adding 0.2 mL of distilled water will yield a concentration of 500 μg/mL

Buffer: Each vial contains 4 mg Trehalose, 0.9 mg NaCl, 0.2 mg Na2HPO4.

Lagerung: 4 °C,-20 °C

Informationen zur Lagerung: After reconstitution, the CHD4 antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.

Details zu CHD4

Target: CHD4 (Chromodomain Helicase DNA Binding Protein 4 (CHD4))

Andere Bezeichnung: CHD4

Hintergrund: CHD4 antibody detects Chromodomain-helicase-DNA-binding protein 4, also called Mi2-beta, a nuclear ATP-dependent chromatin remodeler encoded by the CHD4 gene on chromosome 12p13.31. CHD4 is a member of the CHD family (chromodomain helicase DNA-binding proteins) and serves as the catalytic core of the nucleosome remodeling and deacetylase (NuRD) complex. This complex couples ATP-dependent chromatin remodeling with histone deacetylation to regulate gene transcription, DNA repair, and replication. CHD4 is highly expressed in proliferating cells, hematopoietic lineages, and neurons, where it orchestrates transcriptional repression and chromatin organization.

As a key nuclear regulator, CHD4 modulates chromatin accessibility and transcriptional silencing by repositioning nucleosomes and recruiting histone-modifying enzymes. It interacts with co-repressors, including MTA1-3 and HDAC1/2, within the NuRD complex to establish repressive chromatin states. CHD4's helicase and chromodomain motifs enable recognition of methylated histones and remodeling of nucleosomal DNA, linking epigenetic signals to transcriptional control. It functions in diverse pathways such as cell cycle progression, stem cell maintenance, and DNA damage repair.

CHD4 antibody identifies a protein that interacts with PARP1 and BRCA1 at sites of DNA double-strand breaks, coordinating chromatin remodeling and homologous recombination. Through this association, CHD4 contributes to the DNA damage response (DDR), facilitating repair factor recruitment and checkpoint activation. Mutations or misregulation of CHD4 impair genomic stability and can lead to carcinogenesis or developmental disorders. CHD4 also associates with replication protein A (RPA) and proliferating cell nuclear antigen (PCNA), supporting chromatin reassembly during DNA synthesis.

Structurally, CHD4 contains two N-terminal plant homeodomain (PHD) zinc fingers, tandem chromodomains for methylated histone recognition, an ATPase/helicase domain for chromatin remodeling, and a C-terminal region mediating protein-protein interactions. This modular structure allows CHD4 to integrate epigenetic marks with mechanical chromatin rearrangement. It is part of the CHD family of SNF2-like ATPases that also includes CHD3 and CHD5, all involved in transcriptional regulation and chromatin remodeling.

Dysfunction of CHD4 is linked to various diseases. Somatic mutations have been identified in endometrial carcinoma, chronic lymphocytic leukemia, and glioblastoma. Germline CHD4 mutations cause Sifrim-Hitz-Weiss syndrome, characterized by developmental delay, craniofacial abnormalities, and cardiac defects. Pathway analysis places CHD4 in the chromatin remodeling, DNA repair, and cell cycle regulation pathways. It also co-localizes with HDAC1/2 and MTA proteins in nuclear repressor complexes, reinforcing its central role in chromatin dynamics.

Immunohistochemical staining using CHD4 antibody shows strong nuclear localization in proliferating and stem-like cells. The CHD4 antibody from NSJ Bioreagents is a high-quality reagent for studying chromatin remodeling, epigenetic silencing, and DNA repair mechanisms.

UniProt: Q14839