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  3. Alkaline Phosphatase, Calf intestinal

Alkaline Phosphatase, Calf intestinal  (Synonyms: Apase, Calf intestinal)

Cat. No.: HY-P2818E
Instruction de manipulation Technical Support

Alkaline Phosphatase (Apase), Calf intestinal is an alkaline phosphatase from Calf intestinal, and is one of the most active alkaline phosphatases. Alkaline Phosphatase, Calf intestinal is an orally active membrane-bound glycoprotein that catalyzes the hydrolysis of phosphate monoesters at alkaline pH. Alkaline Phosphatase, Calf intestinal reduces myeloperoxidase activity and bacterial translocation. Alkaline Phosphatase, Calf intestinal improves survival rate of mice infected with E. coli. Alkaline Phosphatase, Calf intestinal improves TNBS-induced colon inflammation.

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Alkaline Phosphatase, Calf intestinal

Alkaline Phosphatase, Calf intestinal Chemical Structure

CAS No. : 9001-78-9

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Description

Alkaline Phosphatase (Apase), Calf intestinal is an alkaline phosphatase from Calf intestinal, and is one of the most active alkaline phosphatases. Alkaline Phosphatase, Calf intestinal is an orally active membrane-bound glycoprotein that catalyzes the hydrolysis of phosphate monoesters at alkaline pH. Alkaline Phosphatase, Calf intestinal reduces myeloperoxidase activity and bacterial translocation. Alkaline Phosphatase, Calf intestinal improves survival rate of mice infected with E. coli. Alkaline Phosphatase, Calf intestinal improves TNBS-induced colon inflammation[1][2][3][4][5][6].

In Vitro

Instructions
1. Dissolve the enzyme in 30 U/μL 10 mM Tris-HCl (pH8.0), 1 mM MgCl2, 50 mM KCl, 0.1 mM ZnCl2. Fresh preparation is recommended.
2. Add the following reagents to a 1.5 mL centrifuge tube to dephosphorylate DNA:
1) 1-20 pmol DNA fragment
2) 1-2 μL Alkaline Phosphatase
3) 5 μL 500 mM Tris-HCl pH 9.0, 10 mM MgCl2
4) Add sterile ddH2O to 50 μL
Note: Single-stranded DNA or DNA with 5' protruding ends is recommended to be incubated at low temperature, while blunt-ended DNA or DNA with 3' protruding ends is recommended to be incubated at higher temperature.
3. Mix well and incubate at 37°C or 50°C for 30 min. Alternatively, incubate at 37°C for 15 min, then incubate at 50°C for 15 min.
4. Extract twice with phenol/chloroform/isoamyl alcohol (25:24:1).
Note: Before phenol extraction, it is recommended to incubate it at 56°C for 30 min in a solution containing 5 mM EDTA, 0.5% SDS, and 50 μg/mL Proteinase K to completely inactivate alkaline phosphatase. Incubate at 75°C for 10 min before phenol extraction for better inactivation. 5. Extract with chloroform/isoamyl alcohol (24:1).
6. Add 2.5 μL 3 M NaCl (final concentration 150 mM), 125 μL (2.5 times volume) pre-cooled ethanol, mix well, and place at -20°C for 30-60 min to precipitate DNA.
4 Centrifuge, completely remove ethanol, and dissolve DNA in an appropriate amount of deionized water (<20 μL).

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

In Vivo

Alkaline Phosphatase, Calf intestinal (1.5 units; i.v.) increases the survival rate of mice injected with a lethal dose of E. coli bacteria[1].
Alkaline Phosphatase, Calf intestinal (0.15 IU/g; i.v.; once; either 5 min before or 15 min after cecal ligation and puncture) reduces cytokine concentrations in plasma and peritoneal lavage fluid, decreases transaminase activity in plasma and myeloperoxidase activity in the lung in a murine cecal ligation and puncture model of polymicrobial sepsis[2].
Alkaline Phosphatase, Calf intestinal (5000 U; i.p.) significantly reduces postoperative peritoneal adhesion formation in mice[3].
Alkaline Phosphatase, Calf intestinal (700 U/kg day; p.o. or intrarectal administration) ameliorates TNBS-elicited colonic inflammation and reduces bacterial translocation in rats[4].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model: Female Wistar rats (175-225 g) + TNBS-induced colitis model[4]
Dosage: 700 U/kg day (oral group: delivered in 1% methylcellulose with 0.2 mM MgCl2; intrarectal group: delivered in 1% methylcellulose with 0.2 mM MgCl2)
Administration: Oral gavage (p.o.) or intrarectal administration
Result: Presented a reduction in colonic weight to length ratio and overall damage score (rectal administration group).
Normalized the expression of S100A8 mRNA, a marker of neutrophil infiltration (rectal administration group).
Showed a reduction of IL-1β and LCN2 colonic expression (rectal administration group).
Had a less marked effect on some endpoints compared to the rectal administration group (p.o. group).
Counteracted bacterial translocation effectively (p.o. group and rectal administration group).
CAS No.
Appearance

Liquid

Color

Colorless to light yellow

SMILES

[Alkaline Phosphatase, Calf intestinal]

Livraison

Room temperature in continental US; may vary elsewhere.

Stockage

Please store the product under the recommended conditions in the Certificate of Analysis.

Pureté et documentation

Références
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    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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Alkaline Phosphatase, Calf intestinal
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