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Grade Molecular Biology Thermosensitive Alkaline Phosphatase

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Guangzhou Dongsheng Biotech Co., Ltd
City:guangzhou
Province/State:guangdong
Country/Region:china
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Grade Molecular Biology Thermosensitive Alkaline Phosphatase

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Brand Name :GDSBio
Model Number :E1013
Certification :/
Place of Origin :China
MOQ :300 U
Price :USD 31.5-76.5/300 U
Payment Terms :L/C, D/A, D/P, T/T, Western Union, MoneyGram
Supply Ability :100 Bag/Bags Per Day
Delivery Time :8 work days
Packaging Details :small package or bulk distribute or OEM
Product Name :Thermosensitive Alkaline Phosphatase
Cat. No./Spec. :E1013-A/300 U; E1013-B/1,000 U; E1013-C/5,000 U
Appearance :colourless
Application :Dephosphorylation of DNA, RNA, and nucleotides
Classification :General Reagents
Grade :molecular biology
Logo Printing :With Logo Printing
Transport Package :Packing
Production Capacity :100 Bag/Bags Per Day
Storage Conditions :Store at -20°C
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Thermosensitive Alkaline Phosphatase

Cat. No./Spec.: E1013-A/300 U; E1013-B/1,000 U; E1013-C/5,000 U
Concentration: 1 U/µL

Product Description
Thermosensitive Alkaline Phosphatase is a novel alkaline phosphatase that exhibits activity in commonly used restriction
endonuclease buffers as well as PCR buffers. This enzyme catalyzes the release of 5' and 3' phosphate groups in DNA, RNA, and nucleotides. Additionally, it can remove phosphate groups from proteins. Thermosensitive Alkaline Phosphatase is capable of dephosphorylating all types of DNA termini within 10 minutes at 37°C. The enzyme is inactivated by heat at 75°C within 5 minutes. Consequently, there is no need to remove the alkaline phosphatase before ligation.

Storage Condition & Shelf Life
Store at -20°C. The product is valid for 2 years.

Source
Recombinant E. coli strain containing the alkaline phosphatase gene cloned from bacteria.

Unit Definition
One unit is defined as the amount of enzyme required to dephosphorylate the 5'-ends of 1 μg of linearized pUC57 DNA in DSAP Buffer at 37°C within 10 minutes.

Scope of Application
- Dephosphorylation of cloned vector DNA to prevent re-circularization during ligation.
- Simultaneous enzymatic cleavage and dephosphorylation of vector DNA.
- Purification of PCR products: nucleotide degradation of PCR products before sequencing.
- Depehosphorylation of the 5'-ends of nucleic acids before T4 polynucleotide kinase labeling.
- Other applications requiring dephosphorylation of DNA and RNA substrates.
- Dephosphorylation of proteins.

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