Applied Biosystems™

Sequenase Version 2.0 DNA Polymerase

Catalog number:  70775Y200UN

 Related applications:

DNA Sequencing

| Sanger Sequencing

Error loading your content!

  Catalog number
Select a plan
Unit size
Price ({{currency}}) Availability Qty
{{product.sku}} {{product.sku}} also known as {{product.formattedSku}} 
{{product.availability.message}}
Pro add-ons

Your on-site stock

›› {{supplyCenter.scName}}({{scProduct.stockOnHand}} In stock)
›› {{supplyCenter.scName}}(Out of stock)
›› {{supplyCenter.scName}}
This item is not currently available on-site. Depending on your Supply Center settings you may be able to add the item to cart above else use the Order Non-Stocked Items' tab on the Supply Center home page.
Back to top

Description

Description:
Sequenase™ Version 2.0 DNA Polymerase is a genetically engineered form of T7 DNA polymerase. Unlike the wild-type enzyme it has virtually no 3'→5' exonuclease activity. Sequenase Version 2.0 is highly processive, incorporates nucleotide analogs (dlTP, thio-dNTPs, dideoxy-NTPs, etc.), is not impeded by secondary structures, and can carry out strand displacement synthesis. It is an excellent enzyme for dideoxy-sequencing, and is useful in other applications, especially where the absence of associated exonuclease activity is desirable. Sequenase Version 2.0 has two subunits, one is the E. coli protein thioredoxin (MW 12,000) and the other is a genetically engineered version of bacteriophage T7 gene 5 protein (MW 76,000). The genetic changes in this subunit (a deletion of 28 amino acids accomplished by in vitro mutagenesis) eliminate all measurable exonuclease activity without changing the DNA polymerase activity.

Properties:
Molecular Weight: Consists of two subunits, modified T7 gene 5 protein (76 kDa) and E. coli
Thioredoxin (12 kDa)
Optimum pH: 7.5
Optimum Temperature: 37°C
Requirements for Divalent Cation: Mg2+, Mn2+

Purity:
Greater than 95% pure as determined by SDS-PAGE.Tested for contaminating double- and single-stranded endonucleases and exonucleases.

Storage Buffer:
20mM potassium phosphate (pH 7.4), 1mM DTT, 0.1mM EDTA, 50% glycerol.

Assay Conditions:
The reaction mixture (100 µL) contains 40mM Tris-HCl (pH 7.5), 10mM MgCl2, 5mM DTT, 0.3mM dNTPs, and 5 µg M13mp18 pre-annealed to 5 pmol M13 universal primer. The enzyme is added to the pre-warmed (37 °C) reaction mixture; incubation is at 37 °C for 1 min.

Unit Definition:
One unit of enzyme catalyzes the incorporation of 1 nmol of nucleotide into acid insoluble form in 30 sec at 37 °C.

Concentration:
13 units/µL

Functional Test:
DNA sequencing with the Sequenase Version 2.0 DNA Sequencing Kit (PN 70770).

Functionally Tested 5X Sequenase Reaction Buffer (1 ml included, PN 70702):
200mM Tris-HCl (pH 7.5), 100mM MgCl2, 250mM NaCl

Sequenase Dilution Buffer (1 ml included, PN 70765):
10mM Tris-HCl (pH 7.5), 5mM DTT, 0.1mM EDTA.

References:
Tabor, S. and Richardson, C. C. (1989) J. Biol. Chem. 264, 6447-6458.
Wang, D., Coscoy, L., Zylberberg, M., Avila, P. C., Boushey, H. A., Ganem, D. and DeRisi, J. L. (2002) Proc Natl. Acad. Sci. USA, 99, 15687-15692.
Paris, M. (1992) Comments 18, (No. 3), United States Biochemical Corporation, Cleveland, Ohio.
Tabor, S. and Richardson, C. C. (1987) Proc.Natl. Acad Sci. USA 84, 4767-4771.
Tabor, S. and Richardson, C. C. (1989) Proc.Natl. Acad. Sci. USA 86, 4076-4080.
For Research Use Only. Not for use in diagnostic procedures.

Specifications

Polymerase: Genetically-Engineered form of T7 DNA Polymerase
Product Size: 200 units

Documents

Manuals & protocols