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商品編號


P7080L



品牌


Enzymatics



公司


Enzymatics,inc



公司分類(lèi)


Ultrapure Polymerases



Size

2,000 U

商品信息

T4 DNA Polymerase


Product Description

T4 DNA Polymerase catalyzes the extension of a primed DNA template in the 5′→ 3′ direction. This enzyme exhibits a powerful 3′→ 5′ exonuclease activity, while lacking any inherent 5′→ 3′ exonuclease or strand displacement functions.

Source of Protein
Purified from a strain of?
E. coli
?that expresses the recombinant T4 DNA Polymerase gene.

Supplied in

100 mM KPO
4
1.0 mM DTT
0.1 mM EDTA
50% glycerol
pH 6.5 @ 25°C

Supplied With
B0110 (10X Blue Buffer)

10X Blue Buffer (B0110)
500 mM NaCl
100 mM Tris-HCl
100 mM MgCl
2
10 mM DTT
pH 7.9 @ 25°C

Unit Definition
One unit is defined as the amount of enzyme that will incorporate 10 nmol of dNTP into acid-precipitable material in 30 minutes at 37°C.



Quality Control Analysis

Unit Characterization Assay
Unit activity was measured using a 2-fold serial dilution method. Dilutions of enzyme were made in 1X reaction buffer and added to 50 ?L reactions containing Calf Thymus DNA, 1X Blue Buffer,?
3
H-dTTP and 100 ?M dNTPs. Reactions were incubated 10 minutes at 37°C, plunged on ice, and analyzed using the method of Sambrook and Russell (
Molecular Cloning, v3, 2001, pp. A8.25-A8.26
)

Protein Concentration (OD
280
) Measurement
A 2.0 ?L sample of enzyme was analyzed at OD
280
?using a
Nanodrop
ND-1000 spectrophotometer standardized using a 2.0 mg/ml BSA sample (
Pierce
Cat #23209) and blanked with product storage solution. The observed average measurement of 3 replicate samples was converted to mg/mL using an extinction coefficient of 128,440 and molecular weight of 103,609 Daltons.

SDS-Page (Physical Purity Assessment)
2.0 ?L of enzyme solution was loaded on a denaturing 4-20% Tris-Glycine SDS-PAGE gel flanked by a broad-range MW
Marker
and 2.0 ?L of a 1:100 dilution of the sample. Following electrophoresis, the gel was stained and the samples compared to determine physical purity. The acceptance criteria for this test requires that the aggregate mass of contaminant bands in the concentrated sample do not exceed the mass of the protein of interest band in the dilute sample, confirming greater than 99% purity of the concentrated sample.



Contamination Tests

Single-Stranded Exonuclease Activity
A 50 ?L reaction containing 10,000 cpm of a r
ADI
olabeled single-stranded DNA substrate and 10 ?L of enzyme solution incubated for 4 hours at 37°C resulted in greater than 80% release of TCA-soluble counts.

Double-Stranded Exonuclease Activity
A 50 ?L reaction containing 5,000 cpm of a r
ADI
olabeled double-stranded DNA substrate and 10 ?L of enzyme solution incubated for 4 hours at 37°C resulted in greater than 50% release of TCA-soluble counts.

Double-Stranded Endonuclease Activity
A 50 ?L reaction containing 0.5 ?g of pBR322 DNA and 10 ?L of enzyme solution incubated for 4 hours at 37°C resulted in no visually discern
IBL
e conversion to nicked circular DNA as determined by agarose gel electrophoresis.

E.coli
16S rDNA Contamination Test
Replicate 5 ?L samples of enzyme solution were denatured and screened in a TaqMan qPCR assay for the presence of contaminating
E.coli
genomic DNA using oligonucleotide primers corresponding to the 16S rRNA locus. The acceptance criterion for the test is the threshold cycle count (C
t
) produced by the average of 3 replicate no template control samples. Based on the correlation between the no template control C
t
values, and standard curve data, the detection limit of this assay is <10 copies genome/sample.


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Product Information



T4 DNA Polymerase


Part Number
P7080L
Price
$363
Concentration
3,000 U/ml
Unit Size
2,000 U


SDS

Available on request








Product Specification*


Storage Temperature
-15 to -25°C


Test

Specification


Purity (SDS-PAGE)
>99%
Specific Activity
5,555 U/mg
SS Exonuclease
Functional
DS Exonuclease
Functional
DS Endonuclease
30 U = no conversion
E.coli
DNA Contamination
30 U < 10 copies





* For a detailed summary of assay conditions and data, refer to the Quality Controls Analysis section.

References


Tabor, S. and Struhl, K. (1989) In DNA-Dependent DNA Polymerases. F. M. Ausebel, R. Brent, R. E. Kingston, D. D. Moore, J. G. Seidman, J. A. Smith and K. Struhl (Eds.), Current Protocols in Molecular
BIOLOG
y, pp. 3.5.10-3.5.12. 2. Sambrook, J., Fritsch, E.F. and Maniatis, T. (1989) Molecular Cloning: A Laboratory Manual, (2nd Ed.), 5.44-5.47.

Dale, R., McClure, B. and Houchins, J. (1985) Plasmid, 13, 31-40.

Kunkel, T.A., Roberts, J.D. and Zakour, R.A. (1987) R. Wu and L. Grossman (Eds.), Methods Enzymol., 154, pp. 367-382. San Diego: Academic Press.

Panet, A., van de Sande, J.H., Loewen, P.C. and Khorana, H.G. (1973) Biochemistry, 12, 5045-5050.




Limitations of Use
This product was developed, manufactured, and sold for in vitro use only. The product is not suitable for admi
NIST
ration to humans or animals. SDS sheets relevant to this product are available upon request.