Modifying Enzymes
Cayman Chemical Hexnoyl-Coenzyme AsodIum s 5mg
A medium-chain fatty acyl CoA; the preferred acyl donor substrate for GOAT; a precursor in the biosynthesis of olivetolic acid
Sigma Aldrich Fine Chemicals Biosciences Cellulase from Trichoderma reesei ATCCÂ 26921 lyophilized powder, >=1 unit/mg solid | 9012-54-8 | MFCD00081510 | 10KU
Cellulase from Trichoderma reesei ATCCÂ 26921 lyophilized powder, >=1 unit/mg solid | 9012-54-8 | MFCD00081510 | 10KU
C LECTA GMBH DENARASE 25 kU, R&D Enzymes & Nucleases
For process development of biologicals such as viral vectors and vaccines The enzyme cleaves all forms of DNA and RNA and enables a simpler more efficient downstream process - Purity 99% - Activity 250 U/ul - Formulation buffered aqueous glycerol solution- Storage -20C - Produced in conformity with ISO 9001 standard- Manufacturing free of animal-derived raw materials and antibiotics- Depending on your application 10-100 U/ml is needed - Net price excluding VAT and shipment costs
c-LEcta will ship the Products, as the case may be and at its sole discretion, either directly from Leipzig, Germany, or from c-LEcta’s third party service provider in the US. In the latter case, c-LEcta has already incurred all costs and fees related to the import of the Products into the US. Such costs and fees will be passed on by c-LEcta to the customer without any deductions or surcharges, if the Products are shipped from c-LEcta’s third party service provider in the US to the customer
Cayman Chemical Oleoyl-L-carnItInchlorIde 10mg
A long-chain acylcarnitine and GlyT2 inhibitor (IC50 = 340 nM); selective for GlyT2 over GlyT1 (IC50 = >10,000 nM); plasma levels are increased in patients with chronic kidney disease or end-stage renal disease receiving incident hemodialysis and these are associated with cardiovascular mortality
New England Biolabs, Inc. AMV Reverse Transcriptase – 1000 units
Avian Myeloblastosis Virus (AMV) Reverse Transcriptase is an RNA-directed DNA polymerase. This enzyme can synthesize a complementary DNA strand initiating from a primer using RNA (cDNA synthesis) or single-stranded DNA as a template.
Worthington Biochemical Corporation DEOXYRIBONUCLEASE I, RECOMBINA
Recombinant Bovine pancreatic Deoxyribonuclease 1 produced in Pichia pastoris. Chromatographically purified. Free of animal derived components, RNases, and proteases. A lyophilized powder containing glycine as a stabilizer.
Sigma Aldrich Fine Chemicals Biosciences Crotonoyl coenzyme A trili5MG
REAGENT Crotonoyl coenzyme A trili5MG
Sigma Aldrich Fine Chemicals Biosciences N Glycosidase f recombinan
Peptide-N-glycosidase f Peptide-N4-(acetyl-beta-glucosaminyl)-asparagine amidase
Sigma Aldrich Fine Chemicals Biosciences Proteinase K from Tritirachium album lyophilized powder, >=30 units/mg protein | 39450-01-6 | MFCD00132129 | 500MG
Proteinase K from Tritirachium album lyophilized powder, >=30 units/mg protein | 39450-01-6 | MFCD00132129 | 500MG
Discovery Life Sciences HUM CYP2C8+REDUCTASE+B5 0.5NMO
Human CYP2C8 + P450 Reductase + Cytochrome b5 SUPERSOMES, 0.5 nmole cytochrome P450 in 0.5 ml. Store at -80degreeC Catalytic assay: paclitaxel-6(alpha)-hydroxylase activity, representative catalytic activity: 2,200 pmole/(mg x min)
Discovery Life Sciences HUMAN CYP1A2+REDUCTASE 0.5NMOL
Human CYP1A2 + P450 Reductase SUPERSOMES 0.5 nmole cytochrome P450 in 0.5mL This activity is catalyzed by CYP1A2 which is expressed from human CYP1A2 cDNA using a baculovirus expression system
Alkali Scientific ASI™ Proteinase K Powder, UltraPure Grade, 1000mg, Store at -20°C
Proteinase K Powder, UltraPure Grade, store at -20°C, 1000mg
New England Biolabs, Inc. T4 RNA Ligase 1 (ssRNA Ligase) – 5000 units
T4 RNA Ligase 1 catalyzes the ligation of a 5' phosphoryl-terminated nucleic acid donor to a 3' hydroxyl-terminated nucleic acid acceptor through the formation of a 3' - 5' phosphodiester bond with hydrolysis of ATP to AMP and PPi. Substrates include single-stranded RNA and DNA as well as dinucleoside pyrophosphates.
ABclonal Technology T7 Endonuclease I
T7 Endonuclease I (T7 Endo I, T7EI)，can recognize and cleave non-perfectly mismatched DNA, cruciform DNA structures, holliday structures or junctions and Heteroduplex DNA. The cleavage site is at the first, second or third phosphodiester bond that is 5? end to the mismatch.