Product Name: DHX16 Antibody
Species Reactivity: Human
Tested Applications: ELISA, WB
Applications: DHX16 antibody can be used for detection of DHX16 by ELISA at 1:62500. DHX16 antibody can be used for detection of DHX16 by western blot at 0.125 μg/mL, and HRP conjugated secondary antibody should be diluted 1:50,000 – 100,000.
User Note: Optimal dilutions for each application to be determined by the researcher.
Predicted Molecular Weight: 115 kDa
Immunogen: Antibody produced in rabbits immunized with a synthetic peptide corresponding a region of human DHX16.
Host Species: Rabbit
Purification: Antibody is purified by peptide affinity chromatography method.
Physical State: Lyophilized
CAS NO.: 162011-90-7
Product: Rofecoxib
Buffer: Antibody is lyophilized in PBS buffer with 2% sucrose. Add 50 μL of distilled water. Final antibody concentration is 1 mg/mL.
Concentration: 1 mg/ml
Storage Conditions: For short periods of storage (days) store at 4˚C. For longer periods of storage, store DHX16 antibody at -20˚C. As with any antibody avoid repeat freeze-thaw cycles.
Clonality: Polyclonal
Conjugate: Unconjugated
Alternate Names: DHX16, DBP2, PRP8, Prp2, DDX16, PRPF2, PRO2014
Accession NO.: NP_003578
Protein Ino: 255982614
Official Symbol: DHX16
Geneid: 8449
Background: 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 a functional homolog of fission yeast Prp8 protein involved in cell cycle progression. This gene is mapped to the MHC region on chromosome 6p21.3, a region where many malignant, genetic and autoimmune disease genes are linked.
PubMed ID:http://aac.asm.org/content/38/7/1628.abstract
