| Catalog # | Availability | Size | Quantity | Unit Price | Save For Later Wish List | |
|---|---|---|---|---|---|---|
| RCP2321-10 | 7 days | 10 µg | $120.00 |
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| RCP2321-50 | 7 days | 50 µg | $290.00 | |||
| RCP2321-1 | 7 days | 1 mg | $3,840.00 |
Product Overview | |
| Name | TANK Human (1-119) |
|---|---|
| Description | |
| TRAF Family Member-Associated NFKB Activator Human Recombinant (1-119 a.a.) | |
| Accession (Primary) | Q92844 |
| Synonyms | |
| Taq Plus DNA Polymerase, Taq Plus DNA, TaqPDNA. | |
| Source | |
| Recombinant E.coli contains Thermus aquaticus polymerase gene. | |
| Formulation | |
| 5U/ µl. | |
| Stability | |
| Stable for 5 days at 10°C, for longer period of time store at -20°C. | |
| Unit Definition | |
| One unit of the enzyme catalyzes the incorporation of 10nmole of deoxyribonucleotides into a polynucleotide fraction in 30 min at 74°C. | |
| Note | |
| All reagents, including Taq Plus, should be mixed immediately before use. | |
| Storage Buffer | |
| 20mM Tris-HCl (pH 8.0), 1mM DTT, 0.1mM EDTA, 100mM KCl, Stabilizers, and 50%glycerol. | |
| Reaction Conditions | |
| DNA synthesis is performed in 100?l of mixture containing 20-200 µm dNTPs, 0.3-1 µm Promers, 0.1-0.250 mg of template DNA, 10 ?l of 10 x reaction buffer and 2.5-5 units of Taq Plus. Mix the reaction gently, centrifuge briefly and then overlay with light mineral oil. Initially, denature the reaction by incubating at 95? for 5 minutes and then cool to 40-68? for 5 minutes to allow the primers to anneal to the template DNA. | |
| 10X Reaction Buffer | |
| 200 mM TrisHCI (pH 8.8) 100 mM KCI 100 mM (NH4)2SO4 20 mM Mg SO4 1% Triton X-100 1 mg/ml bovine serum albumin (BSA). | |
| Optimization of DNA Synthesis | |
| It is important to ad the reaction components in the following order1. H2O. 2. 10 x reaction buffer. 3. dNTPs. 4. DNA template and primers. 5. Taq Plus. | |
| Precautions | |
| TANK Human (1-119) is for research use only and not for use in diagnostic or therapeutic procedures. | |
Target Information: ( Q92844 ) | |
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