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Takara sapphireamp fast pcr master mix

Manufactured by Takara Bio

TaKaRa SapphireAmp Fast PCR Master Mix is a ready-to-use solution for performing fast and efficient PCR amplification. It contains all the necessary components, including a high-fidelity DNA polymerase, dNTPs, and reaction buffer, optimized for rapid thermal cycling.

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2 protocols using takara sapphireamp fast pcr master mix

1

Genotyping Snx5 Knockout Mice

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C57BL/6J mice were obtained from The Jackson Laboratory and all mouse strains used in this study were backcrossed to female C57BL/6J breeders for more than ten generations. Snx5−/− mice were generated by the UC DAVIS Knockout Mouse Project (KOMP) Repository (https://www.komp.org/) and have been previously described23 (link). Genomic DNA from mice was prepared from mouse tail using DirectPCR Lysis Reagent (Viagen Biotech) and Proteinase K (Roche). Mouse genotypes were determined by PCR using TaKaRa SapphireAmp Fast PCR Master Mix (Clontech) and the following primer pairs: Snx5 WT-1, 5’-GCTTTGCCTCTGATTTGGATCTCC-3’; Snx5 WT-2, 5’-CTAAGACAATAAAACCCACCGGGCG-3’; Snx5 KO-1, 5’-GACATGAGCACACTGTTAGTGCAGG-3’; Snx5 KO-2, 5’-GAGATGGCGCAACGCAATTAATG-3’. The PCR conditions are as follows: 1 min at 94°C, 35 cycles of amplification stage (5 sec at 98°C, 5 sec at 55°C and 5 sec at 72°C) and 5 min at 72°C. Snx5+/+ genomic DNA yields a 405-bp band; Snx5−/− genomic DNA yields a 386-bp band; Snx5+/− genomic DNA yields both a 405-bp band and a 386-bp band.
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2

Genotyping Snx5 Knockout Mice

Check if the same lab product or an alternative is used in the 5 most similar protocols
C57BL/6J mice were obtained from The Jackson Laboratory and all mouse strains used in this study were backcrossed to female C57BL/6J breeders for more than ten generations. Snx5−/− mice were generated by the UC DAVIS Knockout Mouse Project (KOMP) Repository (https://www.komp.org/) and have been previously described23 (link). Genomic DNA from mice was prepared from mouse tail using DirectPCR Lysis Reagent (Viagen Biotech) and Proteinase K (Roche). Mouse genotypes were determined by PCR using TaKaRa SapphireAmp Fast PCR Master Mix (Clontech) and the following primer pairs: Snx5 WT-1, 5’-GCTTTGCCTCTGATTTGGATCTCC-3’; Snx5 WT-2, 5’-CTAAGACAATAAAACCCACCGGGCG-3’; Snx5 KO-1, 5’-GACATGAGCACACTGTTAGTGCAGG-3’; Snx5 KO-2, 5’-GAGATGGCGCAACGCAATTAATG-3’. The PCR conditions are as follows: 1 min at 94°C, 35 cycles of amplification stage (5 sec at 98°C, 5 sec at 55°C and 5 sec at 72°C) and 5 min at 72°C. Snx5+/+ genomic DNA yields a 405-bp band; Snx5−/− genomic DNA yields a 386-bp band; Snx5+/− genomic DNA yields both a 405-bp band and a 386-bp band.
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