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Restriction enzymes, modifying enzymes, buffering solutions, inhibitors, and substrates for use in clinical, research, and general laboratory procedures.
Macerozyme R-10Macerating enzyme from Rhizopus sp. suitable for the isolation of plant cells and can be used in combination with cellulase.Specification:Used in plant protoplast preparation to digest cell wall prior to oranelle isolation.A multi-component enzyme mixture containing approximately: * Cellulase: 0.1 U/mg * Hemicellulase: 0.25 U/mg * Pectinase: 0.5 U/mgSource: Rhizopus sp.Solubility: Soluble in water
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Macerozyme R-10Macerating enzyme from Rhizopus sp. suitable for the isolation of plant cells and can be used in combination with cellulase.Specification:Used in plant protoplast preparation to digest cell wall prior to oranelle isolation.A multi-component enzyme mixture containing approximately: * Cellulase: 0.1 U/mg * Hemicellulase: 0.25 U/mg * Pectinase: 0.5 U/mgSource: Rhizopus sp.Solubility: Soluble in water
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Lysozyme Enzyme used in purification protocols of genomic and plasmid DNA to lyse bacterial cells.Ultra Pure GradeSource: Hen Egg White (also called Hen Egg Lysozyme or HEL.)Activity(25 C): >20,000U/mgAlbumin: None detectedSalmonella: None detected
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RNase H (Ribonuclease H ) is an endoribonuclease that specifically hydrolyzes the phosphodiester bonds of RNA which is hybridized to DNA. This enzyme does not digest single or double-stranded DNA.
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Klenow Fragment (3' to 5' exo-) is an N-terminal truncation of DNA Polymerase I which retains polymerase activity, but has lost the 5' to 3' exonuclease activity and has mutations (D355A, E357A) which abolish the 3' to 5' exonuclease activity.
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The Endoglycosidase Reaction Buffer Pack contains four buffers: 10X Glycobuffer 2, 10X Glycobuffer 3, 10X Glycoprotein Denaturing Buffer and 10% NP-40, most commonly used in endoglycosidase reactions.
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Exonuclease T (Exo T), also known as RNase T, is a single-stranded RNA or DNA specific nuclease that requires a free 3' terminus and removes nucleotides in the 3' to 5' direction. Exonuclease T can be used to generate blunt ends from RNA or DNA molecules that have 3 extensions.
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E. coli DNA Ligase catalyzes the formation of a phosphodiester bond between the 5'-phosphate and the 3'-hydroxyl of two adjacent DNA strands in duplex DNA with cohesive ends. It is not appreciably active on blunt-ended substrates. E. coli DNA Ligase uses NAD as a cofactor and can be heat-inactivated.
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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.
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Elastase, Human Neutrophil: 100 UG; Salt-Free lyophilized solid.; MW 29,500; EC = 0.985; Activity: 20-22 units per mg protein; Purity: > =95% by SDS-PAGE. This native protein is prepared and purified from whole blood in the Athens Research & Tech lab.
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