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    Results for Enzymes ( 22571 )

      • Ref: H00768211-P01
        Sizes: 10 ug, 25 ug
        From: DKK3,165.00

        Human RELL1 full-length ORF (AAH39540.1, 1 a.a. - 271 a.a.) recombinant protein with GST tag at N-terminal.

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      • Ref: KA6943
        Sizes: 1 Kit
        From: DKK3,998.00

        Peroxidase (HRP) Conjugation Kit is designed for antibody conjugation with HRP.

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      • Ref: KA6944
        Sizes: 1 Kit
        From: DKK9,578.00

        Peroxidase (HRP) Conjugation Kit is designed for antibody conjugation with HRP.

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      • Ref: KA6945
        Sizes: 1 Kit
        From: DKK28,800.00

        Peroxidase (HRP) Conjugation Kit is designed for antibody conjugation with HRP.

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      • From: DKK5,850.00

        Alkaline phosphatase (ALP) Conjugation Kit is designed for antibody conjugation with ALP.

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      • From: DKK7,523.00

        Alkaline phosphatase (ALP) Conjugation Kit is designed for antibody conjugation with ALP.

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      • From: DKK9,128.00

        Alkaline phosphatase (ALP) Conjugation Kit is designed for antibody conjugation with ALP.

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      • From: DKK413.00

        PNLIP is an enzyme which belongs to the lipase family. Secreted from the pancreas, PNLIP is the primary lipase that hydrolyzes dietary fat molecules in the human digestive system, converting triglyceride substrates found in ingested oils to monoglycerides and free fatty acids. Bile salts secreted from the liver and stored in gallbladder are released into the duodenum where they coat and emulsify large fat droplets into smaller droplets, thus increasing the overall surface area of the fat, which allows the lipase to break apart the fat more effectively. The resulting monomers (2 free fatty acids and one 2-monoacylglycerol) are then moved by way of peristalsis along the small intestine to be absorbed into the lymphatic system by a specialized vessel called a lacteal.

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      • From: DKK413.00

        Degrades extracellular matrix. Proposed to play a role in breast cancer invasion and metastasis. Exhibits trypsin-like activity as defined by cleavage of synthetic substrates with Arg or Lys as the P1 site.Defects in ST14 are a cause of ichthyosis autosomal recessive with hypotrichosis (ARIH). ARIH is a skin disorder characterized by congenital ichthyosis associated with the presence of less than the normal amount of hair.

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