Modifying Enzymes
Sigma Aldrich Fine Chemicals Biosciences Peroxidase from horseradish Type VI, essentially salt-free, lyophilized powder, ≥250 units/mg solid (using pyrogallol) | 9003-99-0 | MFCD00071339 | 10ku
Peroxidase from horseradish Type VI, essentially salt-free, lyophilized powder, ≥250 units/mg solid (using pyrogallol) | Purity: | MW: | 9003-99-0 | MFCD00071339 | 10ku
Sigma Aldrich Fine Chemicals Biosciences Proteinase K from Tritirachium album ≥3.0 unit/mg solid, lyophilized powder | 39450-01-6 | MFCD00132129 250mg
Proteinase K from Tritirachium album ≥3.0 unit/mg solid, lyophilized powder | 39450-01-6 | MFCD00132129 | 250mg
Sigma Aldrich Fine Chemicals Biosciences Proteinase K from Tritirachium album lyophilized powder, BioUltra, >=30 units/mg protein, for molecular biology | 39450-01-6 | MFCD00132129 | 10MG
Proteinase K from Tritirachium album lyophilized powder, BioUltra, >=30 units/mg protein, for molecular biology | 39450-01-6 | MFCD00132129 | 10MG
Sigma Aldrich Fine Chemicals Biosciences Malic Dehydrogenase from porcine heart >=600 units/mg protein (biuret), ammonium sulfate suspension | MFCD00131567 | 5KU
Malic Dehydrogenase from porcine heart >=600 units/mg protein (biuret), ammonium sulfate suspension | MFCD00131567 | 5KU
Sigma Aldrich Fine Chemicals Biosciences Proteinase K from Tritirachium album Reagents designed and manufactured under current ISO 13485 certification. | 39450-01-6 | MFCD00132129 | 5ML
Proteinase K from Tritirachium album Reagents designed and manufactured under current ISO 13485 certification. | 39450-01-6 | MFCD00132129 | 5ML
Sigma Aldrich Fine Chemicals Biosciences beta-Glucuronidase from Helix pomatia Type H-1, partially purified powder, >=300,000 units/g solid | 9001-45-0 | MFCD00130629 | 100KU
beta-Glucuronidase from Helix pomatia Type H-1, partially purified powder, >=300,000 units/g solid | 9001-45-0 | MFCD00130629 | 100KU
Sigma Aldrich Fine Chemicals Biosciences Beta-Galactosidase from Escherichia Coli | 9031-11-2 | MFCD00130623 | 1ku
Beta-Galactosidase from Escherichia Coli | 9031-11-2 | MFCD00130623 | 1ku
QA Bio Inc QA-Bio, Inc. • PNGase F • native Elizabethkingia miricola • 200 µls
PNGase F - 200 µls -E. miricola • Removes N-linked Glycans • No Glycerol, EDTA, or NaCl - Enzyme remains fully active for 4+ days at 37˚C. • Used by Biopharmaceutical Labs Around the World in FDA/EMEA Assays since 2002.
Biotium Double Stranded DNA (dsDNA)(AE-2), 0.2mg/mL
This monoclonal antibody is part of a new panel of reagents, which recognizes subcellular organelles or compartments of human cells. These markers may be useful in identification of these organelles in cells, tissues, and biochemical preparations. This MAb recognizes the double stranded DNA in human cells. It can be used to stain the nuclei in cell or tissue preparations and can be used as a nuclear marker in human cells. This MAb produces a homogeneous staining pattern in the nucleus of normal and malignant cells.,Double Stranded deoxyribonucleic acid (ds DNA) is the genetic material of all cells and many viruses and is a polymer of nucleotides. The monomer consists of phosphorylated 2-deoxyribose N-glycosidically linked to one of four bases, adenine, cytosine, guanine or thymine. These are linked together by 3',5'-phosphodiester bridges. In the Watson-Crick double-helix model, two complementary strands are wound in a right-handed helix and held together by hydrogen bonds be
Sigma Aldrich Fine Chemicals Biosciences beta-Glucosidase from almonds lyophilized powder, >=2 units/mg solid | 9001-22-3 | MFCD00130628 | 2.5KU
beta-Glucosidase from almonds lyophilized powder, >=2 units/mg solid | 9001-22-3 | MFCD00130628 | 2.5KU
New England Biolabs, Inc. T5 Exonuclease – 5000 units
T5 Exonuclease degrades DNA in the 5 to 3 direction. T5 Exonuclease is able to initiate nucleotide removal from the 5 termini or at gaps and nicks of linear or circular dsDNA. However, the enzyme does not degrade supercoiled dsDNA. T5 Exonuclease also has ssDNA endonuclease activity.
New England Biolabs, Inc. RNase If – 5000 units
Ribonuclease If (RNase If) is an RNA endonuclease which will cleave at all RNA dinucleotide bonds leaving a 5'hydroxyl and 2',3' cyclic monophosphate. It has a preference for single-stranded RNA over double-stranded RNA. RNase If is a recombinant protein fusion of RNase I (from E. coli) and maltose-binding protein. It has identical activity to RNase I.
New England Biolabs, Inc. Endonuclease VIII – 1000 units
Endonuclease VIII from E. coli acts as both an N-glycosylase and an AP-lyase. The N-glycosylase activity releases damaged pyrimidines from double-stranded DNA, generating an apurinic (AP site). The AP-lyase activity cleaves 3' and 5' to the AP site leaving a 5' phosphate and a 3' phosphate. Damaged bases recognized and removed by Endonuclease VIII include urea, 5, 6- dihydroxythymine, thymine glycol, 5-hydroxy-5- methylhydantoin, uracil glycol, 6-hydroxy-5, 6-dihydrothymine and methyltartronylurea. While Endonuclease VIII is similar to Endonuclease III, Endonuclease VIII has and lyase activity while Endonuclease III has only lyase activity.