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APMB-RO

Roche

Alkaline Phosphatase

solution, from bovine (calf) intestine, 2 units/μg protein, optimum pH 7.5-9.5

Synonyme(s) :

ALP, CAP, CIAP, calf intestinal phosphatase, cip, orthophosphoric monoester phosphohydrolase

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About This Item

Numéro de classification (Commission des enzymes):
Code UNSPSC :
12352204

Source biologique

bovine (calf) intestine

Niveau de qualité

Forme

solution

Activité spécifique

2 units/μg protein

Conditionnement

pkg of 1,000 U (10713023001 [1 U/μl])
pkg of 1,000 U (11097075001 [20 U/μl])

Fabricant/nom de marque

Roche

Paramètres

37 °C optimum reaction temp.

pH optimal

7.5-9.5

Conditions d'expédition

wet ice

Température de stockage

2-8°C

Description générale

Alkaline phosphatase (ALP) is a glycoprotein that is expressed ubiquitously. This enzyme is bound to the cell membrane. Activation of ALP requires essential co-factors, such as zinc and magnesium. Alkaline phosphatase catalyzes the removal of phosphate groups from various compounds that are phosphorylated. Alkaline phosphatase from calf intestine hydrolyzes 5′-monophosphate groups from both DNA and RNA. It can also hydrolyze 5′-diphosphate and 5′-triphosphate groups from RNA. Hence, intestinal ALP is one of the commonly used enzymes in molecular cloning.

Application

Use this preparation of calf intestinal alkaline phosphatase to remove 5′-terminal phosphates from DNA or RNA and immunoprecipitated RNA samples.
Note: The 11097075001 preparation has a high concentration of enzyme (20 U/μl), which is convenient for large-scale experiments. The 10713023001 preparation is a lower concentration (1 U/μl), which is convenient for small-scale experiments.

Séquence

AP is a zinc-containing enzyme with 4 atoms zinc per molecule (Efstradiatis, 1977).

Définition de l'unité

One unit of alkaline phosphatase is the enzyme activity which hydrolyzes 1 mol of 4-nitrophenyl phosphate in 1 minute at +37 °C under assay conditions.
Note: According to Moessner et al. 5 units alkaline phosphatase (+37 °C; diethanolamine buffer) correspond to 1 unit alkaline phosphatase (+25 °C; glycine/NaOH buffer).

Unit Conversion: Approx. 3.6 U (MB grade AP)
[+37 °C, 4-NPP as substrate, diethanolamine as buffer, pH 9.8] = 1 U [+25 °C, 4.NPP as substrate, glycine as buffer, pH 10.5].

Volume Activity: 20 U/μl for the 11097075001 preparation. 1 U/μl for the 10713023001 preparation.

Forme physique

10713023001: Enzyme solution (1 U/μl) in storage buffer, pH 7.6 (20 °C)

11097075001: Enzyme solution (20 U/μl) in storage buffer, pH 7.6 (20 °C)

Notes préparatoires

Working solution: Storage buffer: 25 mM Tris-HCl, 1 mM MgCl2, 0.1 mM ZnCl2, glycerol 50% (v/v), pH 7.6 (4 °C).
Storage conditions (working solution): Dilutions (1 to 5 U/μl) of MB grade AP in the storage buffer are stable for 17 months at 2 to 8 °C.
Higher Dilutions (~0.01 U/μl) should be made fresh daily and kept at 2 to 8 °C.
Preventing self-ligation of vectors during cloning
If a linearized vector lacks a 5′ phosphate, it cannot ligate to itself or form concatamers that contain multiple copies of the vector. Thus, the product of the ligation reaction is predominantly recombinant DNA (vector + DNA insert), rather than religated plasmid.
Inactivation: Add 1/10 volume of EGTA to the reaction mix and incubate at +65°C for 10 minutes. To ensure complete inactivation of enzyme, extract the mix with phenol/chloroform/isoamyl alcohol to remove all protein.

Autres remarques

For general laboratory use.

Code de la classe de stockage

12 - Non Combustible Liquids

Classe de danger pour l'eau (WGK)

WGK 1

Point d'éclair (°F)

does not flash

Point d'éclair (°C)

does not flash


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Consulter la Bibliothèque de documents

Qiang Zhao et al.
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Saline-alkali (SA) stress induces excessive reactive oxygen species (ROS) accumulation in plant cells, resulting in oxidative damages of membranes, lipids, proteins, and nucleic acids. Melatonin has antioxidant protection effects in living organisms and thus has received a lot of attention.
Erratum: Mapping Argonaute and conventional RNA-binding protein interactions with RNA at single-nucleotide resolution using HITS-CLIP and CIMS analysis.
Michael J Moore et al.
Nature protocols, 11(3), 616-616 (2016-02-26)
Xiangyu Chen et al.
PLoS biology, 13(12), e1002329-e1002329 (2015-12-20)
Interhomolog crossovers promote proper chromosome segregation during meiosis and are formed by the regulated repair of programmed double-strand breaks. This regulation requires components of the synaptonemal complex (SC), a proteinaceous structure formed between homologous chromosomes. In yeast, SC formation requires
O Brenna et al.
The Biochemical journal, 151(2), 291-296 (1975-11-01)
A crude preparation of alkaline phosphatase (EC 3.1.3.1) from calf intestinal mucosa was purified by affinity chromatography on Sepharose-bound derivatives of arsanilic acid, which was found to be a competitive inhibitor of the enzyme. Three biospecific adsorbents were prepared for
Anne Kristin Aksaas et al.
Genes & cancer, 2(8), 841-851 (2012-03-07)
Serine/arginine-rich splicing factor 1 (SRSF1), previously designated SF2/ASF, belongs to a family of SR proteins that regulate constitutive and alternative splicing. SRSF1 expression is increased in tumors from several tissues and elicits changes in key target genes involved in tumor

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