Type: | in situ hybridisation probe |
Identifier: | Dgcr8 probeA |
Entity Detected: | Dgcr8, DiGeorge syndrome critical region gene 8 ( MGI:2151114) |
Sequence: | sense strand is shown
>Dgcr8 probeA
TCGGCAGAGGGGTGGTGTAAGAATAAAAGAGTTGGGAAACAATTAGCATCTCAGAAAATCCTTCAGCTAC
TGCACCCACATGTCAAGAACTGGGGTTCCTTACTACGCATGTATGGTCGTGAGAGCAGCAAAATGGTCAA
GCAGGAGACCTCTGACAAGAGTGTGATAGAGCTACAGCAGTATGCCAAGAAGAACAGGCCCAACCTTCAC
ATCCTGAGCAAGCTACAAGAAGAGATGAAGAGGCTGGCTGCAGAGCGGGAGGAGACTCGGAAGAAACCCA
AGATGTCAATTGTAGCATCTGCCCAGCCTGGTGGTGAGCCCTTGTGCACAGTCGATGTATGAGGTAGGCA
GCATGGGCCAACAGTGCTACCCAGGAGAGACCATCAGCCACACATCATCACTCTGCAGCTCCAGGCCTCC
AACCTAAGTTCCTTCCCTGTGGCAGGGTCTGGGCTCTGGCTCTGGCACATGGGGACAGCTGTGACTACAC
AGTACACATGCAAAGAAGCAGTTCTGGACAAGCTGCTCTCAATGTGACTGGATATACTTAAGGATCAGTC
ATAAGT
|
Notes: | The Dgcr8 probe used in ths study by Shiohama et al., 2003 [PMID:12705904] is described as follows: "In situ hybridization was performed using digoxigenin labeled antisense riboprobes synthesized from the mouse cDNA clone Dgcr8. The cDNA clone was obtained from I.M.A.G.E. clones (Accession No. AA217940), linearized with restriction endonucleases, and riboprobe was synthesized by T3, T7 RNA polymerase (Ampliscribe T3/T7 High Yield Transcription Kits, Epicentre Technologies, Madison, WI)." |
Chemistry: | RNA |
Strand: | antisense |
Label: | digoxigenin |