IS215UCVEM09A
USD $1213 - $2222 /Piece
Min.Order:1 Piece
Temporal Ming sheng automation equipment co., LTD
Brand:GE
Type:IS215UCVEM09A
Origin:the United States
Warranty: 365 days
Colour: new/used
Shipping method: Courier delivery
Products are widely used in metallurgy, petroleum, glass, aluminum manufacturing, petrochemical industry, coal mine, papermaking, printing, textile printing and dyeing, mechanical, electronic manufacturing, automobile manufacturing, plastic machinery, electric power, water conservancy, water treatment/environmental protection, boiler heating, energy, power transmission and distribution and so on.
Spare parts spare parts, the main DCS control system of PLC system and the robot system spare parts,
Brand advantage: Allen Bradley, BentlyNevada, ABB, Emerson Ovation, Honeywell DCS, Rockwell ICS Triplex, FOXBORO, Schneider PLC, GE Fanuc, Motorola, HIMA, TRICONEX, Prosoft etc. Various kinds of imported industrial parts
Applications Post-PCR DNA Clean-up Efficient desalting of DNA with the removal of DNA polymerases, primers, and free dNTPs. DNA Clean-up From Enzymatic Reactions Efficient desalting of DNA with the removal of modifying enzymes, RNA polymerases, ligases, kinases, nucleases, phosphatases, endonucleases, etc. Post-Reverse Transcription (RT) & cDNA Clean-up Efficiently purifies DNA following RT, either as a DNA/RNA complex or as single stranded cDNA following chemical hydrolysis of the RNA template. Plasmid DNA Clean-up Efficiently purifies plasmid DNA from “home-made” preparations of cell free lysates or from commercial kits. Plasmid DNA purified and concentrated using the DCC® has proven an excellent substrate for high quality DNA sequencing. Isotope and Dye Removal Efficiently removes unincorporated fluorescent (i.e., AMCA, FITC, BIO, DIG, Cy3, Cy5, FAM, etc.) and radiolabeled dNTP derivatives from DNA following in vitro labeling reactions. Purification of M13 ssDNA The DCC® can be used for the rapid isolation of single stranded M13 phage DNA directly from phage-infected E. coli culture supernatant. ✓ For purification of short DNA or RNA oligonucleotides ≥ 16 nt, use the Oligo Clean & Concentrator (D4060, D4061). ✓ For ChIP (Chromatin Immunoprecipitation) sample cleanup, use the ChIP DNA Clean & Concentrator® (D5201, D5205) for high quality DNA from any step in a standard ChIP protocol. ✓ For post-cycle sequencing samples, use the ZR Sequencing DNA Clean-up Kit™ (D4050, D4051) for dye blob elimination. ✓ For samples containing PCR inhibitors, use the OneStep™ PCR Inhibitor Removal Kit (D6030, D6035).
Selected Citations Li, N. (2010). Whole genome DNA methylation analysis based on high throughput sequencing technology. Methods, 52 (3), 221-232. Lee, EJ. (2011). Targeted bisulfite sequencing by solution selection and massively parallel sequencing. Nucleic Acids Research, 39(19), e127, doi:10.1093/nar/gkr598 Papageorgiou, EA. (2009). Sites of differential DNA methylation between placenta and peripheral blood. Am J Pathol, 174 (5), 1609-1618. Ferguson, A.A. et al. (2009). Retrofitting ampicillin resistant vectors by recombination for use in generating C. elegans transgenic animals by bombardment. Plasmid, 62, 140-145.