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PCR |
Name: |
PAR2 |
Type: |
PCR |
System: |
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Genetic Element: |
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Ampl. Length: |
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Ampl. Position: |
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Sequence Size [bp]: |
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AnnTemp [°C]: |
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Taxonomy: |
Cattle (Beef (general)) |
Temp. Time Program: |
Cycling conditions :<br>One cycle of DNA denaturation for 2 min at 94 °C;<br>35 three-step cycles 94 °C for 30 sec<br>61 °C for 30 sec<br>and 72 °C for 1 min<br>Last extension for 3 min at 72 °C |
Device: |
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Reagents: |
PCR Mix:<br>Primer PAR2-DIR (5 μM) 2 μl<br>Primer PAR2-REV (5 μM) 2 μl<br>PCR buffer 10x 5 μl<br>MgCl2 (25 mM) 3 μl<br>dNTPs (2 mM) 5 μl<br>Taq DNA polymerase (5 U/μl) 0,4 μl<br>H2O<br>ADN 100 ng<br>Total volume 50 μl |
nPrimers: |
2 |
Organisation: |
CRA-W |
PCR Description: |
Original PCR protocol developed by CRA-W and INRA for the detection of the Sv, 2.1 and 2.2 alleles of the PAR2 gene |
Sequence: |
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LOD [copy]: |
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LOQ [copy]: |
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Efficiency [%]: |
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Remarks: |
Original PCR protocol developed by CRA-W and INRA for the detection of the Sv, 2.1 and 2.2 alleles of the PAR2 gene |
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