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Rabbit Anti-CHD1L/FITC Conjugated antibody
background:
CHD1L is a 897 amino acid protein encoded by the human gene CHD1L. The CHD family of proteins are ATP-dependent chromatin remodeling enzymes, which combine chromodomains, with SWI2/SNF2 ATPase/helicase motifs and DNA-binding capability. Chromodomains are protein regions of about 40-50 amino acid residues found in proteins associated with chromatin remodeling and manipulation. The domain is highly conserved among both plants and animals and is found in a large variety of proteins from many genomes. CHD1L and CHD1 share most homology within two internal helicase domains.
Function:
DNA helicase which plays a role in chromatin-remodeling following DNA damage. Targeted to sites of DNA damage through interaction with poly(ADP-ribose) and functions to regulate chromatin during DNA repair. Able to catalyze nucleosome sliding in an ATP-dependent manner. Helicase activity is strongly stimulated upon poly(ADP-ribose)-binding.
Subunit:
Interacts with PARP1; interacts only when PARP1 is poly-ADP-ribosylated (PARylated).
Subcellular Location:
Nucleus. Localizes at sites of DNA damage. Probably recruited to DNA damage sites by PARylated PARP1.
Tissue Specificity:
Frequently overexpressed in hepatomacellular carcinomas.
Similarity:
Belongs to the SNF2/RAD54 helicase family.
Contains 1 helicase ATP-binding domain.
Contains 1 helicase SLCterminal domain.
Contains 1 Macro domain.
Database links:
Entrez Gene: 9557 Human
Entrez Gene: 13658 Mouse
Omim: 613039 Human
SwissProt: Q86WJ1 Human
SwissProt: Q9CXF7 Mouse
Unigene: 191164 Human
Unigene: 41447 Mouse
Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
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