PCR Supplies
Boca Scientific Inc Tth DNA Polymerase, 2500 units
Tth DNA Polymerase is a recombinant, thermostable enzyme with intrinsic reverse transcription (RT) activity. It can be used in both RT-PCR and regular PCR and can reverse transcript and amplify fragments up to 2-3 kb. Tth DNA Polymerase was isolated from eubacterium Thermus thermophilus strain HB8 and is expressed in E.coli. It has a highly processive 5-3 polymerase activity, but no 3-5 exonuclease activity. It also does not have RNase activity.
Medchemexpress LLC 1-Methylcytosine | 1122-47-0 | 125.13 | 25 MG
1-Methylcytosine is a methylated form of the DNA base cytosine. It is utilized as a nucleobase of hachimoji DNA, where it forms a pair with Isoguanine. It has been observed to exhibit weak antiproliferative activity against cervical cancer cells and can be utilized in cervical cancer research.
- Weakly inhibits proliferation of human cervical cancer HeLa cells with an IC50 value of 12 μM.
- Shows no antiproliferative activity against human tumor cell lines such as MiaPaCa-2, SW620, MCF-7, and H460 (IC50 >100 μM for all).
- Functions as a nucleoside antimetabolite/analog.
- Involved in cell cycle/DNA damage pathway.
Qiagen Beverly Inc DNA POLYMERASE I
DNA Polymerase; DNA Polymerase I; Conc. 10,000 U/ml; 5,000 U; incl. 10X buffer
As One International Inc Taq DNA Polymerase 5 U/ul , 500U
Taq DNA Polymerase is a thermostable recombinant DNA polymerase, which exhibits very high activity in primer extension and other molecular biology applications. The enzyme is isolated from Thermus aquaticus and has a molecular weight of approximately 94 kDa. Taq DNA Polymerase has both a 5' to 3' DNA polymerase and a 5' to 3' exonuclease activity. The enzyme lacks a 3' to 5' exonuclease activity (no proofreading ability). Taq DNA Polymerase leaves an A prime overhang, which makes the enzyme ideal for TA cloning. No reaction buffers included.
As One International Inc Taq DNA Polymerase 5 U/ul 10x Standard Buffer, Magnesium free and Triton free, 2,500U
Taq DNA Polymerase is a thermostable recombinant DNA polymerase, which exhibits very high activity in primer extension and other molecular biology applications. The enzyme is isolated from Thermus aquaticus and has a molecular weight of approximately 94 kDa. Taq DNA Polymerase has both a 5' to 3' DNA polymerase and a 5' to 3' exonuclease activity. The enzyme lacks a 3' to 5' exonuclease activity (no proofreading ability). Taq DNA Polymerase leaves an A prime overhang, which makes the enzyme ideal for TA cloning. Included with Taq is Triton/magnesium free 10x Standard Buffer.
As One International Inc Taq DNA Polymerase 5 U/ul 10x Standard Buffer, Triton free, 500U
Taq DNA Polymerase is a thermostable recombinant DNA polymerase, which exhibits very high activity in primer extension and other molecular biology applications. The enzyme is isolated from Thermus aquaticus and has a molecular weight of approximately 94 kDa. Taq DNA Polymerase has both a 5' to 3' DNA polymerase and a 5' to 3' exonuclease activity. The enzyme lacks a 3' to 5' exonuclease activity (no proofreading ability). Taq DNA Polymerase leaves an A prime overhang, which makes the enzyme ideal for TA cloning. Included with Taq is Triton free 10x Standard Buffer.
As One International Inc Taq DNA Polymerase 5 U/ul 10x Standard Buffer, Triton free, 10,000U
Taq DNA Polymerase is a thermostable recombinant DNA polymerase, which exhibits very high activity in primer extension and other molecular biology applications. The enzyme is isolated from Thermus aquaticus and has a molecular weight of approximately 94 kDa. Taq DNA Polymerase has both a 5' to 3' DNA polymerase and a 5' to 3' exonuclease activity. The enzyme lacks a 3' to 5' exonuclease activity (no proofreading ability). Taq DNA Polymerase leaves an A prime overhang, which makes the enzyme ideal for TA cloning. Included with Taq is Triton free 10x Standard Buffer.
As One International Inc Taq DNA Polymerase 5 U/ul 10x Standard Buffer, Magnesium free and Triton free, 500U
Taq DNA Polymerase is a thermostable recombinant DNA polymerase, which exhibits very high activity in primer extension and other molecular biology applications. The enzyme is isolated from Thermus aquaticus and has a molecular weight of approximately 94 kDa. Taq DNA Polymerase has both a 5' to 3' DNA polymerase and a 5' to 3' exonuclease activity. The enzyme lacks a 3' to 5' exonuclease activity (no proofreading ability). Taq DNA Polymerase leaves an A prime overhang, which makes the enzyme ideal for TA cloning. Included with Taq is Triton/magnesium free 10x Standard Buffer.
As One International Inc Red-Taq DNA Polymerase 5 U/ul 10x Ammonium Buffer and 10x Combination Buffer both detergent free, 10,000U
AS ONE Taq DNA Polymerase with red dye is a thermostable recombinant DNA polymerase, which exhibits very high activity in primer extension and other molecular biology applications. Taq contains a red dye which provides easy and quick identification of reactions to which enzyme was added and allows confirmation of complete mixing. The inert dye has no effect on downstream processes. Taq with Red Dye is added directly to the reaction mix and is used in the same manner as standard Taq DNA Polymerase. AS ONE Taq DNA Polymerase with red dye has both a 5' to 3' DNA polymerase and a 5' to 3' exonuclease activity. The enzyme lacks a 3' to 5' exonuclease activity. Taq DNA Polymerase leaves an A prime overhang, which makes the enzyme ideal for TA cloning. Red Taq Polymerase includes Tween/Triton free 10x Ammonium Buffer and 10x Combination Buffer.
As One International Inc Red-Taq DNA Polymerase 5 U/ul 10x Ammonium Buffer and 10x Combination Buffer both detergent free, 500U
AS ONE Taq DNA Polymerase with red dye is a thermostable recombinant DNA polymerase, which exhibits very high activity in primer extension and other molecular biology applications. Taq contains a red dye which provides easy and quick identification of reactions to which enzyme was added and allows confirmation of complete mixing. The inert dye has no effect on downstream processes. Taq with Red Dye is added directly to the reaction mix and is used in the same manner as standard Taq DNA Polymerase. AS ONE Taq DNA Polymerase with red dye has both a 5' to 3' DNA polymerase and a 5' to 3' exonuclease activity. The enzyme lacks a 3' to 5' exonuclease activity. Taq DNA Polymerase leaves an A prime overhang, which makes the enzyme ideal for TA cloning. Red Taq Polymerase includes Tween/Triton free 10x Ammonium Buffer and 10x Combination Buffer.