BAG4 cDNA

ATGTCGGCCC TGAGGCGCTC GGGCTACGGC CCCAGTGACG GTCCGTCCTA CGGCCGCTAC TACGGGCCTG GGGGTGGAGA TGTGCCGGTA CACCCACCTC CACCCTTATA TCCTCTTCGC CCTGAACCTC CCCAGCCTCC CATTTCCTGG CGGGTGCGCG GGGGCGGCCC GGCGGAGACC ACCTGGCTGG GAGAAGGCGG AGGAGGCGAT GGCTACTATC CCTCGGGAGG CGCCTGGCCA GAGCCTGGTC GAGCCGGAGG AAGCCACCAG GAGCAGCCAC CATATCCTAG CTACAATTCT AACTATTGGA ATTCTACTGC GAGATCTAGG GCTCCTTACC CAAGTACATA TCCTGTAAGA CCAGAATTGC AAGGCCAGAG TTTGAATTCT TATACAAATG GAGCGTATGG TCCAACATAC CCCCCAGGCC CTGGGGCAAA TACTGCCTCA TACTCAGGGG CTTATTATGC ACCTGGTTAT ACTCAGACCA GTTACTCCAC AGAAGTTCCA AGTACTTACC GTTCATCTGG CAACAGCCCA ACTCCAGTCT CTCGTTGGAT CTATCCCCAG CAGGACTGTC AGACTGAAGC ACCCCCTCTT AGGGGGCAGG TTCCAGGATA TCCGCCTTCA CAGAACCCTG GAATGACCCT GCCCCATTAT CCTTATGGAG ATGGTAATCG TAGTGTTCCA CAATCAGGAC CGACTGTACG ACCACAAGAA GATGCGTGGG CTTCTCCTGG TGCTTATGGA ATGGGTGGCC GTTATCCCTG GCCTTCATCA GCGCCCTCAG CACCACCCGG CAATCTCTAC ATGACTGAAA GTACTTCACC ATGGCCTAGC AGTGGCTCTC CCCAGTCACC CCCTTCACCC CCAGTCCAGC AGCCCAAGGA TTCTTCATAC CCCTATAGCC AATCAGATCA AAGCATGAAC CGGCACAACT TTCCTTGCAG TGTCCATCAG TACGAATCCT CGGGGACAGT GAACAATGAT GATTCAGATC TTTTGGATTC CCAAGTCCAG TATAGTGCTG AGCCTCAGCT GTATGGTAAT GCCACCAGTG ACCATCCCAA CAATCAAGAT CAAAGTAGCA GTCTTCCTGA AGAATGTGTA CCTTCAGATG AAAGTACTCC TCCGAGTATT AAAAAAATCA TACATGTGCT GGAGAAGGTC CAGTATCTTG AACAAGAAGT AGAAGAATTT GTAGGAAAAA AGACAGACAA AGCATACTGG CTTCTGGAAG AAATGCTAAC CAAGGAACTT TTGGAACTGG ATTCAGTTGA AACTGGGGGC CAGGACTCTG TACGGCAGGC CAGAAAAGAG GCTGTTTGTA AGATTCAGGC CATACTGGAA AAATTAGAAA AAAAAGGATT ATGA

BAG4, BAG-4, SODD, BAG4, ATGD0089-10 µg, ATGD0089-20 µg, ATGD0089-50 µg, ATGD0089-100 µg, ATGD0089-250 µg, ATGD0089-500 µg, ATGD0089-1 mg, ATGD0089-10, ATGD0089-20, ATGD0089-50, ATGD0089-100, ATGD0089-250, ATGD0089-500, ATGD0089-1

1. Centrifuge at 7000rpm for 1 minute.; ;2. Carefully open the vial and add 100 µL of sterile water to dissolve the DNA.; ; Each tube contains approximately 10 µg of lyophilized plasmid.

This shuttle vector contains the complete ORF. It is inseted BamH I to Xho I. The gene insert contains multiple cloning sites which can be used to easily cut and transfer the gene and recombination site into your expression vector.