TA cloning for sars cov 2 nucleocapsid protein. - (Feb/19/2021 )

hi everyone. ı want to do recombinant nucleocapsid protein for sars cov 2. ı will use TA clonig (pet sumo cloning kit) . which primer do you recomend for gen . or how ı can find right primer. please help me. its very important for me. 

And your purpose is to produce protein from the nucleocapsid expression vector? If so, you most likely want primers that bind at the very start and very end of the nucleoprotein sequence respectively.

thank you my friend. you say ı did it . it s ok. but ı find a article have a primer . ı went to pubmed. than ı use blast for primer. pubmed  didnt find (article primer ) in NCBI Reference Sequence for sars cov 2. ı think also ı search my primer in google . google didnt find my primer. 

can you tray my primer. 

nucleocapsid gene.

ATGTCTGATAATGGACCCCAAAATCAGCGAAATGCACCCCGCATTACGTTTGGTGGACCCTCAGATTCAACTGGCAGTAACCAGAATGGAGAACGCAGTGGGGCGCGATCAAAACAACGTCGGCCCCAAGGTTTACCCAATAATACTGCGTCTTGGTTCACCGCTCTCACTCAACATGGCAAGGAAGACCTTAAATTCCCTCGAGGACAAGGCGTTCCAATTAACACCAATAGCAGTCCAGATGACCAAATTGGCTACTACCGAAGAGCTACCAGACGAATTCGTGGTGGTGACGGTAAAATGAAAGATCTCAGTCCAAGATGGTATTTCTACTACCTAGGAACTGGGCCAGAAGCTGGACTTCCCTATGGTGCTAACAAAGACGGCATCATATGGGTTGCAACTGAGGGAGCCTTGAATACACCAAAAGATCACATTGGCACCCGCAATCCTGCTAACAATGCTGCAATCGTGCTACAACTTCCTCAAGGAACAACATTGCCAAAAGGCTTCTACGCAGAAGGGAGCAGAGGCGGCAGTCAAGCCTCTTCTCGTTCCTCATCACGTAGTCGCAACAGTTCAAGAAATTCAACTCCAGGCAGCAGTAGGGGAACTTCTCCTGCTAGAATGGCTGGCAATGGCGGTGATGCTGCTCTTGCTTTGCTGCTGCTTGACAGATTGAACCAGCTTGAGAGCAAAATGTCTGGTAAAGGCCAACAACAACAAGGCCAAACTGTCACTAAGAAATCTGCTGCTGAGGCTTCTAAGAAGCCTCGGCAAAAACGTACTGCCACTAAAGCATACAATGTAACACAAGCTTTCGGCAGACGTGGTCCAGAACAAACCCAAGGAAATTTTGGGGACCAGGAACTAATCAGACAAGGAACTGATTACAAACATTGGCCGCAAATTGCACAATTTGCCCCCAGCGCTTCAGCGTTCTTCGGAATGTCGCGCATTGGCATGGAAGTCACACCTTCGGGAACGTGGTTGACCTACACAGGTGCCATCAAATTGGATGACAAAGATCCAAATTTCAAAGATCAAGTCATTTTGCTGAATAAGCATATTGACGCATACAAAACATTCCCACCAACAGAGCCTAAAAAGGACAAAAAGAAGAAGGCTGATGAAACTCAAGCCTTACCGCAGAGACAGAAGAAACAGCAAACTGTGACTCTTCTTCCTGCTGCAGATTTGGATGATTTCTCCAAACAATTGCAACAATCCATGAGCAGTGCTGACTCAACTCAGGCCTAA

my primer  forward: ATGTCTGATAATGGACCCCA

reverse: TTAGGCCTGAGTTGAGTCAG

do you think this Primer its true.

The look fine for this purpose, assuming you have cDNA from the virus that you can amplify. It would pay to do a Primer BLAST on the primers to ensure that they don't hit host genome significantly. Using the Primer BLAST section for Primer Pair Specificity Checking Parameters, you can either leave it as nr or specify the host genome to BLAST against.

thank you my friend. 

best regards