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Merck

T4GENE32-RO

Roche

T4 Gene 32 Protein

from Escherichia coli(infected with phage T4amN134/amBL292/amE218), solution, optimum pH ~8.0

Synonym(s):

gene 32 protein, t4

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About This Item

UNSPSC Code:
12352202
NACRES:
NA.54

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Product Name

T4 Gene 32 Protein, from Escherichia coli(infected with phage T4amN134/amBL292/amE218), solution, optimum pH ~8.0

biological source

Escherichia coli (infected with phage T4amN134/amBL292/amE218)

form

solution

packaging

pkg of 100 μg (10972983001)
pkg of 500 μg (10972991001)

manufacturer/tradename

Roche

optimum pH

~8.0

storage temp.

−20°C

Quality Level

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This Item
SRP0416DNALIG-ROH7533
biological source

Escherichia coli (infected with phage T4amN134/amBL292/amE218)

biological source

Escherichia coli

biological source

Escherichia coli (NM 989)

biological source

rat

form

solution

form

aqueous solution

form

solution

form

buffered aqueous solution

storage temp.

−20°C

storage temp.

−70°C

storage temp.

−20°C

storage temp.

−70°C

Quality Level

100

Quality Level

-

Quality Level

100

Quality Level

200

packaging

pkg of 100 μg (10972983001), pkg of 500 μg (10972991001)

packaging

pkg of 100 μg

packaging

pkg of 100 U (10481220001 [1 U/μl]), pkg of 500 U (10716359001 [1 U/μl]), pkg of 500 U (10799009001 [5 U/μl])

packaging

-

manufacturer/tradename

Roche

manufacturer/tradename

-

manufacturer/tradename

Roche

manufacturer/tradename

-

Analysis Note

Absence of contaminants
T4 gene 32 protein is incubated with various nucleic acids that serve as potential nuclease substrates. Results are analyzed by gel electrophoresis. Based on these tests, none of the following are detectable in the preparation according to the current Quality Control procedures:
  • nonspecific exo- and endonucleases
  • single-strand DNases (nicking activities)
  • single-strand-specific exonucleases
  • RNases

Application

T4 Gene 32 Protein is a single-strand-specific DNA-binding protein. It may be used for:
  • Optimization of PCR (See "Product Description" below.)
  • Stimulation of in vitro DNA synthesis
  • Stabilization of single-stranded regions of DNA or RNA
  • Site-specific mutagenesis experiments (with T4 DNA polymerase and T4 DNA ligase)
  • Helping restriction enzyme digestions go to completion
  • q-PCR[1]

Biochem/physiol Actions

T4 gene 32 protein is a single-strand specific, helix-destabilizing protein encoded by gene 32 of the phage T4 genome. It is required for the replication of DNA and genetic recombination in Escherichia coli cells that are infected with T4 bacteriophage.[2]

General description

T4 Gene 32 Protein is reported to improve the yield of long PCR products when 0.5 to 1.0 nmol of the protein is included in the reaction. T4 Gene 32 Protein is also reported to increase the yield of PCR products amplified from samples that contain humic acid. The inhibitory effect of humic acid is reduced by a factor of 7 when T4 Gene 32 Protein is included in the PCR (at a concentration of 2.5 μg/100 μl).
The protein is isolated from the triple-mutant T4amN134/ amBL292/ amE 219 defective for the T4 genes 33, 35, and 58 to 61.

Other Notes

For life science research only. Not for use in diagnostic procedures.

Physical form

Protein solution, 1 - 10mg/ml, in storage buffer (20mM Tris-HCl, 100mM NaCl, 1mM EDTA, 0.5mM DTT, 50% glycerol [v/v], pH approximately 8.0)

Preparation Note

Working concentration: 1 to 10 mg/ml

Storage Class

12 - Non Combustible Liquids

wgk

WGK 1

flash_point_f

No data available

flash_point_c

No data available


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M Bittner et al.
The Journal of biological chemistry, 254(19), 9565-9572 (1979-10-10)
Detailed procedures are presented which allow reproducible preparation of T4 gene 32 protein, a helix-destabilizing protein essential for DNA replication and genetic recombination in T4 bacteriophage-infected Escherichia coli cells. Although 32 protein can be purified to better than 99% homogeneity
Pauline Jacob et al.
International journal of environmental research and public health, 12(3), 2967-2983 (2015-03-13)
A two-year monitoring program of Cryptosporidium parvum oocysts, Giardia duodenalis cysts, Escherichia coli, Clostridium perfringens spores and adenovirus was conducted in three large rivers in France used for recreational activities and as a resource for drinking water production. Fifty-liter river

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