Product Name
Potassium Acetate (DDX11), Reagent
Full Product Name
Potassium Acetate
Product Gene Name
DDX11 reagent
[Similar Products]
Research Use Only
For Research Use Only. Not for use in diagnostic procedures.
Chromosome Location
Chromosome: 12; NC_000012.11 (31226779..31257733). Location: 12p11
3D Structure
ModBase 3D Structure for Q96FC9
Purity/Purification
ACS Grade
99.0%
Appearance: White crystalline powder
Solubility (5%): Colorless, clear, complete
Insoluble Matter: 0.005%
pH (5%): 6.5 to 9.0
Chloride: 0.003%
Phosphate: 0.001%
Sulfate: 0.002%
Calcium: 0.005%
Magnesium: 0.002
Molecular Formula
CH3CKO2
Preparation and Storage
Room Temperature
Other Notes
Small volumes of DDX11 reagent vial(s) may occasionally become entrapped in the seal of the product vial during shipment and storage. If necessary, briefly centrifuge the vial on a tabletop centrifuge to dislodge any liquid in the container`s cap. Certain products may require to ship with dry ice and additional dry ice fee may apply.
Product Categories/Family for DDX11 reagent
Biochemicals; Biochem-Inorganic Reagents
NCBI/Uniprot data below describe general gene information for DDX11. It may not necessarily be applicable to this product.
NCBI Accession #
Q96FC9.1
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UniProt Primary Accession #
Q96FC9
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UniProt Secondary Accession #
Q13333; Q86VQ4; Q86W62; Q92498; Q92770; Q92998; Q92999[Other Products]
UniProt Related Accession #
Q96FC9[Other Products]
Molecular Weight
98.14[Similar Products]
NCBI Official Full Name
Probable ATP-dependent RNA helicase DDX11
NCBI Official Synonym Full Names
DEAD/H (Asp-Glu-Ala-Asp/His) box helicase 11
NCBI Official Symbol
DDX11 [Similar Products]
NCBI Official Synonym Symbols
CHL1; KRG2; WABS; CHLR1
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NCBI Protein Information
probable ATP-dependent RNA helicase DDX11; KRG-2; hCHLR1; DEAD/H box protein 11; CHL1-related protein 1; CHL1-like helicase homolog; CHL1-related helicase gene-1; keratinocyte growth factor-regulated gene 2 protein; DEAD/H (Asp-Glu-Ala-Asp/His) box polypeptide 11 (CHL1-like helicase homolog, S. cerevisiae)
UniProt Protein Name
Probable ATP-dependent RNA helicase DDX11
UniProt Synonym Protein Names
CHL1-related protein 1; hCHLR1; DEAD/H box protein 11; Keratinocyte growth factor-regulated gene 2 protein
Protein Family
ATP-dependent DNA helicase
UniProt Gene Name
DDX11 [Similar Products]
UniProt Synonym Gene Names
CHL1; CHLR1; KRG2; hCHLR1; KRG-2 [Similar Products]
UniProt Entry Name
DDX11_HUMAN
NCBI Summary for DDX11
DEAD box proteins, characterized by the conserved motif Asp-Glu-Ala-Asp (DEAD), are putative RNA helicases. They are implicated in a number of cellular processes involving alteration of RNA secondary structure such as translation initiation, nuclear and mitochondrial splicing, and ribosome and spliceosome assembly. Based on their distribution patterns, some members of this family are believed to be involved in embryogenesis, spermatogenesis, and cellular growth and division. This gene encodes a DEAD box protein, which is an enzyme that possesses both ATPase and DNA helicase activities. This gene is a homolog of the yeast CHL1 gene, and may function to maintain chromosome transmission fidelity and genome stability. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Jul 2008]
UniProt Comments for DDX11
DDX11: DNA helicase involved in cellular proliferation. Possesses DNA-dependent ATPase and helicase activities. This helicase translocates on single-stranded DNA in the 5' to 3' direction in the presence of ATP and, to a lesser extent, dATP. Its unwinding activity requires a 5'-single-stranded region for helicase loading, since flush-ended duplex structures do not support unwinding. The helicase activity is capable of displacing duplex regions up to 100 bp, which can be extended to 500 bp by RPA or the cohesion establishment factor, the Ctf18-RFC (replication factor C) complex activities. Stimulates the flap endonuclease activity of FEN1. Required for normal sister chromatid cohesion. Required for recruitment of bovine papillomavirus type 1 regulatory protein E2 to mitotic chrmosomes and for viral genome maintenance. Required for maintaining the chromosome segregation and is essential for embryonic development and the prevention of aneuploidy. May function during either S, G2, or M phase of the cell cycle. Binds to both single- and double-stranded DNA. Defects in DDX11 are the cause of Warsaw breakage syndrome (WBRS). It is a syndrome characterized by severe microcephaly, pre- and postnatal growth retardation, facial dysmorphism and abnormal skin pigmentation. Additional features include high arched palate, coloboma of the right optic disk, deafness, ventricular septal defect, toes and fingers abnormalities. At cellular level, drug-induced chromosomal breakage, a feature of Fanconi anemia, and sister chromatid cohesion defects, a feature of Roberts syndrome, coexist. Belongs to the DEAD box helicase family. DEAH subfamily. DDX11/CHL1 sub-subfamily. 5 isoforms of the human protein are produced by alternative splicing.
Protein type: EC 3.6.4.13; Helicase; Nucleolus
Chromosomal Location of Human Ortholog: 12p11
Cellular Component: nucleoplasm; spindle pole; cytoplasm; nuclear chromatin; nucleolus; midbody; nucleus
Molecular Function: ATP-dependent DNA helicase activity; DNA-dependent ATPase activity; protein binding; RNA binding; metal ion binding; 4 iron, 4 sulfur cluster binding; double-stranded DNA binding; helicase activity; ATP binding; single-stranded DNA binding
Biological Process: cellular protein metabolic process; unfolded protein response, activation of signaling protein activity; viral reproduction; unfolded protein response; nucleobase, nucleoside, nucleotide and nucleic acid metabolic process; sister chromatid cohesion; DNA duplex unwinding
Disease: Warsaw Breakage Syndrome
Research Articles on DDX11
1. A [p.R263Q]) in DDX11 in three affected siblings with severe intellectual disability and many of the congenital abnormalities reported in the Warsaw breakage syndrome (WABS) original case.">Data indicate a homozygous mutation (c.788G>A [p.R263Q]) in DDX11 in three affected siblings with severe intellectual disability and many of the congenital abnormalities reported in the Warsaw breakage syndrome (WABS) original case.
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