Alkaline Phosphatase [CIAP] Stabilized in aqueous solution

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Telephone	1-800-990-8053
Fax	1-800-609-2943
Email	sales@aatbio.com
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Physical properties

Molecular weight	~86 kDa
Solvent	Water

Storage, safety and handling

H-phrase	H303, H313, H333
Hazard symbol	XN
Intended use	Research Use Only (RUO)
R-phrase	R20, R21, R22
Storage	Freeze (< -15 °C); Minimize light exposure
UNSPSC	12171501

Alternative formats

Overview SDS Protocol

See also: Alkaline Phosphatase (ALP)

Molecular weight

~86 kDa

Calf Intestinal Alkaline Phosphatase (CIP or CIAP) nonspecifically catalyzes the dephosphorylation of 5´ and 3´ ends of DNA and RNA phosphomonoesters. CIAP also hydrolyses ribo-, as well as deoxyribonucleoside triphosphates (NTPs and dNTPs). CIAP is useful in many molecular biology applications such as the removal of phosphorylated ends of DNA and RNA for subsequent use in cloning or end-labeling of probes. In cloning, dephosphorylation prevents religation of linearized plasmid DNA. The enzyme acts on 5´ protruding, 5´ recessed and blunt ends. CIAP may also be used to degrade unincorporated dNTPs in PCR reactions to prepare templates for DNA sequencing or SNP analysis. CIAP conjugates have been widely used in immunological assays and tests in combination with a variety of color or fluorogenic AP substrates. AAT Bioquest offers the largest collection of fluorogenic AP substrates for developing AP-based ELISA assays and tests.

Images

Figure 1. Calf Intestinal Alkaline Phosphatase (CIP or CIAP) nonspecifically catalyzes the dephosphorylation of 5´ and 3´ ends of DNA and RNA phosphomonoesters. CIAP also hydrolyses ribo-, as well as deoxyribonucleoside triphosphates (NTPs and dNTPs). CIAP is useful in many molecular biology applications such as the removal of phosphorylated ends of DNA and RNA for subsequent use in cloning or end-labeling of probes. CIAP conjugates have been widely used in immunological assays and tests in combination with a variety of color or fluorogenic AP substrates. AAT Bioquest offers the largest collection of fluorogenic AP substrates for developing AP-based ELISA assays and tests.