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|Tested species reactivity||Tag|
|Host / Isotype||Not Applicable|
|Immunogen||Taq DNA Polymerase|
|Storage buffer||TBS, pH 8, with 2mM Na2PO4, 0.1mM EDTA, 50% glycerol, 1mM DTT|
|Tested Applications||Dilution *|
|Functional Assay (FN)||Assay dependent|
|Inhibition Assays (IA)||Assay dependent|
* Suggested working dilutions are given as a guide only. It is recommended that the user titrate the product for use in their own experiment using appropriate negative and positive controls.
One unit of Taq DNA polymerase incorporates 10 nmol of deoxyribonucleotide into DNA in 30 minutes at 74°C. One unit is defined as the amount of product required to inhibit one unit of Taq DNA polymerase.
PCR Functional Assay Specifications: PCR reactions containing 200 ng, 20 ng and 10 ng of input human genomic DNA yield 40 ng, 10 ng and 5 ng of an 800 bp target, respectively, when observed on an ethidium bromide stained gel.
In a radioactive nucleotide incorporation assay, Taq DNA polymerase activity has been successfully inhibited by 10965-010.
Platinum® Taq Antibody is a proprietary inhibitor which, when bound to Taq DNA polymerase, inactivates polymerase activity. This reagent provides an automatic “hot start” for Taq DNA polymerase in PCR. Hot starts are typically used in PCR to increase sensitivity, specificity, and yield while allowing assembly of reactions at ambient temperatures. The extra time, effort, and contamination risks associated with manual hot start procedures are addressed with the use of Platinum® Taq Antibody.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
Taq DNA polymerase