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Serin protease with very broad range of action: cleaves peptide bonds at the carboxylic side of aliphatic, aromatic, and hydrophobic amino acids. Suitable for the isolation of DNA and RNA (1, 3). Serin protease with very broad range of action: cleaves peptide bonds at the carboxylic side of aliphatic, aromatic, and hydrophobic amino acids. Suitable for the isolation of DNA and RNA (1, 3).
Product Detail
Serine protease with very broad range of action: cleaves peptide bonds at the carboxylic side of aliphatic, aromatic, and hydrophobic amino acids.Suitable for the isolation of DNA and RNA (1, 3). Serine protease with very broad range of action: cleaves peptide bonds at the carboxylic side of aliphatic, aromatic, and hydrophobic amino acids.Suitable for the isolation of DNA and RNA (1, 3).
Product Detail
For the determination of peroxide (1). Used as an indicator enzyme in reactions where peroxide is produced (2). For labelling antibodies in ELISA (3, 4). RZ (= A 403/A 275) = 3.0. For the determination of peroxide (1). Used as an indicator enzyme in reactions where peroxide is produced (2). For labelling antibodies in ELISA (3, 4). RZ (= A 403/A 275) = 3.0.
Product Detail
Serin protease with very broad range of action: cleaves peptide bonds at the carboxylic side of aliphatic, aromatic, and hydrophobic amino acids. Suitable for the isolation of DNA and RNA (1, 3). Serin protease with very broad range of action: cleaves peptide bonds at the carboxylic side of aliphatic, aromatic, and hydrophobic amino acids. Suitable for the isolation of DNA and RNA (1, 3).
Product Detail
A multi-component enzyme system (1). Although the preparation has high cellulase activity (EC 3.2.1.4), it still contains hemicellulases, and it degrades mannans, xylans, galactomannans, pectins and other polysaccharides. Contains about three times as high xylanase activity as Cellulase Onozuka R-10 (cat. no. 16419). Widely used for the isolation of protoplasts, for its ability to degrade cell walls, often in combination with Macerozyme R-10 (cat. no. 28302) (2).Temperature optimum: 50 - 60 °CpH-optimum: pH 4 - 5 A multi-component enzyme system (1). Although the preparation has high cellulase activity (EC 3.2.1.4), it still contains hemicellulases, and it degrades mannans, xylans, galactomannans, pectins and other polysaccharides. Contains about three times as high xylanase activity as Cellulase Onozuka R-10 (cat. no. 16419). Widely used for the isolation of protoplasts, for its ability to degrade cell walls, often in combination with Macerozyme R-10 (cat. no. 28302) (2).Temperature optimum: 50 - 60 °CpH-optimum: pH 4 - 5
Product Detail
Macerozyme R-10 can be used in combination with cellulase "Onozuka R-10" (cat. no. 16419) (1, 2) or with cellulase "Onozuka RS" (cat. no. 16420) for the isolation of plant cells and especially for the isolation of metabolically active protoplasts. Macerozyme R-10 can be used in combination with cellulase "Onozuka R-10" (cat. no. 16419) (1, 2) or with cellulase "Onozuka RS" (cat. no. 16420) for the isolation of plant cells and especially for the isolation of metabolically active protoplasts.
Product Detail
A multi-component enzyme system (1). Although the preparation has high cellulase activity (EC 3.2.1.4), it still contains hemicellulases, and it degrades mannans, xylans, galactomannans, pectins and other polysaccharides. Contains about three times as high xylanase activity as Cellulase Onozuka R-10 (cat. no. 16419). Widely used for the isolation of protoplasts, for its ability to degrade cell walls, often in combination with Macerozyme R-10 (cat. no. 28302) (2).Temperature optimum: 50 - 60 °CpH-optimum: pH 4 - 5 A multi-component enzyme system (1). Although the preparation has high cellulase activity (EC 3.2.1.4), it still contains hemicellulases, and it degrades mannans, xylans, galactomannans, pectins and other polysaccharides. Contains about three times as high xylanase activity as Cellulase Onozuka R-10 (cat. no. 16419). Widely used for the isolation of protoplasts, for its ability to degrade cell walls, often in combination with Macerozyme R-10 (cat. no. 28302) (2).Temperature optimum: 50 - 60 °CpH-optimum: pH 4 - 5
Product Detail
Cellulase Onozuka R-10 is used for the degradation of plant cell walls, usually for the production and isolation of metabolically active protoplasts, often in combination with Macerozyme R-10 (cat. no. 28032) (2).The cellulase Onozuka R-10 is a multi-component enzyme system (1). Although the preparation has high cellulase activity, it contains hemicellulases and degrades mannans, xylans, galactomannans, pectins and other polysaccharides. Temperature optimum: 40 - 50 °CpH-optimum: pH 4 - 5 Cellulase Onozuka R-10 is used for the degradation of plant cell walls, usually for the production and isolation of metabolically active protoplasts, often in combination with Macerozyme R-10 (cat. no. 28032) (2).The cellulase Onozuka R-10 is a multi-component enzyme system (1). Although the preparation has high cellulase activity, it contains hemicellulases and degrades mannans, xylans, galactomannans, pectins and other polysaccharides. Temperature optimum: 40 - 50 °CpH-optimum: pH 4 - 5
Product Detail
Serine protease with very broad range of action: cleaves peptide bonds at the carboxylic side of aliphatic, aromatic, and hydrophobic amino acids.Suitable for the isolation of DNA and RNA (1, 3). Serine protease with very broad range of action: cleaves peptide bonds at the carboxylic side of aliphatic, aromatic, and hydrophobic amino acids.Suitable for the isolation of DNA and RNA (1, 3).
Product Detail
Alkaline phosphatase (ALP) preparation with highly specific activity, especially suitable for conjugation to antibodies and other proteins for ELISA, Western blotting, and histochemical detection (1). Compared to other enzyme conjugates, the substrate conversion reaction of alkaline phosphatase is linear, thus the sensitivity can be increased by a prolonged incubation time. ALP can also be an alternative for tissues with a high level of endogenous peroxidases, as the risk of substrate-related non-specific background staining is low.The enzyme may also be used to dephosphorylate proteins and nucleic acids. To prevent self-ligation the 5'-termini of DNA or RNA are dephosphorylated with alkaline phosphatase. After dephosphorylation the nucleic acids can as well be tagged with radiolabeled phosphate by T4 polynucleotide kinase.Alkaline phosphatase from calf intestine is a dimeric, membrane-derived glycoprotein. The enzyme is most stable in the pH range 7.5 - 9.5 and requires zinc, and magnesium or calcium divalent ions for activity.In 40 % glycerol, containing 6 mM Tris/HCl, 6 mM MgCl2, 0.12 mM ZnCl2, pH ca. 7.6. Alkaline phosphatase (ALP) preparation with highly specific activity, especially suitable for conjugation to antibodies and other proteins for ELISA, Western blotting, and histochemical detection (1). Compared to other enzyme conjugates, the substrate conversion reaction of alkaline phosphatase is linear, thus the sensitivity can be increased by a prolonged incubation time. ALP can also be an alternative for tissues with a high level of endogenous peroxidases, as the risk of substrate-related non-specific background staining is low.The enzyme may also be used to dephosphorylate proteins and nucleic acids. To prevent self-ligation the 5'-termini of DNA or RNA are dephosphorylated with alkaline phosphatase. After dephosphorylation the nucleic acids can as well be tagged with radiolabeled phosphate by T4 polynucleotide kinase.Alkaline phosphatase from calf intestine is a dimeric, membrane-derived glycoprotein. The enzyme is most stable in the pH range 7.5 - 9.5 and requires zinc, and magnesium or calcium divalent ions for activity.In 40 % glycerol, containing 6 mM Tris/HCl, 6 mM MgCl2, 0.12 mM ZnCl2, pH ca. 7.6.
Product Detail
Serin protease with very broad range of action: cleaves peptide bonds at the carboxylic side of aliphatic, aromatic, and hydrophobic amino acids. Suitable for the isolation of DNA and RNA (1, 3). Serin protease with very broad range of action: cleaves peptide bonds at the carboxylic side of aliphatic, aromatic, and hydrophobic amino acids. Suitable for the isolation of DNA and RNA (1, 3).
Product Detail
For the determination of peroxide (1). Used as an indicator enzyme in reactions where peroxide is produced (2). For labelling antibodies in ELISA (3, 4). RZ (= A 403/A 275) = 3.0. For the determination of peroxide (1). Used as an indicator enzyme in reactions where peroxide is produced (2). For labelling antibodies in ELISA (3, 4). RZ (= A 403/A 275) = 3.0.
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