Modifying Enzymes
Worthington Biochemical Corporation HYALURONIDASE PURIFIED 30KU
Chromatographically purified. A dialyzed, lyophilized powder. 37326-33-3
Worthington Biochemical Corporation DEOXYRIBONUCLEASE I 100MG
Partially purified. A lyophilized powder. 9003-98-9
Worthington Biochemical Corporation PHOSPHATASE ALKALINE 250MG
Partially purified. A dried powder. Used in the NF/USP dexamethasone phosphate assay. 9001-78-9
Worthington Biochemical Corporation COLLAGENASE TYPE 2 FI 1000MG
Collagenase, Type 2 (Code: CLS-2), which is filtered through a 0.22 micron membrane and lyophilized in vials. 2593-92-3
Cayman Chemical Precelys 24 User MaIntena 1ea
This kit provides Precellys 24 users with all of the necessary parts to properly maintain their instrument. EAch kit contains: 1 x Precellys 24 White Blocking Plate (2 mL) (Item No. 10422) 2 x Precellys 24 Vacuum Joint (toric joint) (Item No. 10011148) 1 x Precellys 24 Containment Seal (Item No. 10011149)] 1 x Precellys 24 Anti-Rotation Tubing Kit - (Item No. 10011162) [Bertin Catalog S000688-PR240-A.0; Previously SP03119-810-NC011.0]
SIGMA ALDRICH FINE CHEMICALS BIOSCIENCES ANTI-TOPOISOMERASE I-DNA COVAL
NC3728455 ANTI-TOPOISOMERASE I-DNA COVAL
Medchemexpress LLC Lipase, Pseudomonas fluorescens (immobilized) | 9001-62-1 | MFCD00131509 | 500mg
Lipase Pseudomonas fluorescens (Immobilized) comes from Pseudomonas fluorescens and shows good applicability in ester synthesis of food industry the biofuel synthesis the synthesis of enantiomeric pure chiral drugs and so on[1]
ABclonal Technology Exonuclease I (E. coli)
Exonuclease I catalyzes the removal of nucleotides from single-stranded DNA in the 3 to 5 direction, and does not degrade DNA strands with the 3-OH end blocked by phosphoryl or acetyl groups. Exonuclease I has strict substrate specificity and is incapable of degrading double-stranded DNA and RNA.
ABclonal Technology Endonuclease III (Nth)
Endonuclease III (Nth) protein acts as both N-glycosylase and a AP-lyase.The N-glycosylase activity releases damaged pyrimidines from double-stranded DNA, generating a basic (AP site). The AP-lyase activity of the enzyme cleaves 3? to the AP site leaving a 5? phosphate and a 3? ring opened sugar.