WBSCR27 (BC030295) Human Untagged Clone
CAT#: SC123504
WBSCR27 (untagged)-Human Williams Beuren syndrome chromosome region 27 (cDNA clone MGC:40131 IMAGE:5396423), complete cds
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Specifications
Product Data | |
Type | Human Untagged Clone |
Tag | Tag Free |
Symbol | WBSCR27 |
Synonyms | MGC40131 |
Vector | pCMV6-XL5 |
E. coli Selection | Ampicillin (100 ug/mL) |
Mammalian Cell Selection | None |
Sequence Data |
>OriGene sequence for BC030295 edited
GAGCATGGCCCAGGAGGAGGGTGGGAGCCTGCCCGAGGTGCGGGCGCGGGTCAGGGCCGC GCATGGCATCCCCGACCTGGCCCAAAAGCTCCATTTCTATGACCGCTGGGCTCCGGACTA CGACCAGGATGTGGCCACCCTGCTGTACCGTGCGCCCCGCCTCGCAGTGGACTGCCTCAC ACAAGCCCTTCCAGGCCCGCCCCACAGTGCCCTGATCCTGGACGTGGCCTGTGGCACAGG CCTAGTGGCTGCCGAGCTGCGGGCTCCAGGCTTCCTCCAGCTGCATGGGGTGGATGGGAG CCCAGGGATGCTGGAACAGGCCCGGGCCCCCGGCCTCTATCAGCGCCTCAGCCTCTGCAC CCTGGGCCAGGAGCCTCTGCCCAGCCCGGAAGGGACCTTCGACGCGGTGCTGATAGTCGG TGCCCTCAGTGACGGCCAGGTGCCCTGCAATGCGATACCTGAGCTACATGTCACCAAGCC AGGTGGGCTGGTGTGTCTGACCACCAGGACCAACTGGTCCAACCTTCAATACAAGGAGGC TCTGGAGGCCACCCTGGACAGGCTGGAGCAGGCTGGGATGTGGGAAGGCCTGGTGGCCTG GCCTGTGGACCGCCTGTGGACCGCTGGGAGCTGGCTACCTCCGAGCTGGTGGTGGTATCC GGCATCTCTGCCAAGGATGGCTTCATCTCCGGCATTGTCTACCTGTACCGAAAGTGGAAG GCGACCCAGGTTGAGGAAGTGAGATCCAGCCCCCAGCCCCCAGCTGGCCCCTGACTCCAT GTGGCCTTAGCTGGGCCCATCTGCTGGGCCTCCTCTGCCTCCCCTGTAAAATGGGACCTC CGAACCAACCCTGCCCCTCAGAAATGCCCTGCCTATTAAATGAGCTCCCAGAAAAAAAAA AAAAAAAAAAAAAAAAAAAAAA >OriGene 5' read for BC030295 unedited
CCGTTCAGGATTTTGTNATACGACTTTACTATAGGGNCGGCCGCGNAATTCCCGGGGAAT CGTCGACCCACTCGTCCGCTGTTGCCCACACGCCCCAGGCGCGCTGGATTGGCGGAGCAT GGCCCAGGAGGAGGGTGGGAGCCTGCCCGAGGTGCGGGCGCGGGTCAGGGCCGCGCATGG CATCCCCGACCTGGCCCAAAAGCTCCATTTCTATGACCGCTGGGCTCCGGACTACGACCA GGATGTGGCCACCCTGCTGTACCGTGCGCCCCGCCTCGCAGTGGACTGCCTCACACAAGC CCTTCCAGGCCCGCCCCACAGTGCCCTGATCCTGGACGTGGCCTGTGGCACAGGCCTAGT GGCTGCCGAGCTGCGGGCTCCAGGCTTCCTCCAGCTGCATGGGGTGGATGGGAGCCCAGG GATGCTGGAACAGGCCCGGGCCCCCGGCCTCTATCAGCGCCTCAGCCTCTGCACCCTGGG CCAGGAGCCTCTGCCCAGCCCGGAAGGGACCTTCGACGCGGTGCTGATAGTCGGTGCCCT CAGTGACGGCCAGGTGCCCTGCAATGCGATACCTGAGCTACATGTCACCAAGCCAGGTGG GCTGGTGTGTCTGACCACCAGGACCAACTGGTCCAACCTTCAATACAAGGAGGCTCTGGA GGCCACCCTGGACAGGCTGGAGCANGCTGGGATGTGGGAAGGCCTGGTGGCCTGGCCTGT GGACCGCCTGTGGACCGCTGGGAGCTGGCTACCTCCGAGCTGGTGGTGGTATCCGGCATC TCTGCCCAAGATGGCTTCATCTCCGGCATTGTCTACCTGTACCGAAAGTGGAAAGCGACC CCAGTTGAGGAAGTGAGATCCAGCCCCCAGCCCCCAGCTGGCCCCTGACTCCATGTGGCC TTAGCTGGGCCCATCTGCTGGGCCTCCT |
Restriction Sites | Please inquire |
ACCN | BC030295 |
Insert Size | 969 |
OTI Disclaimer | Our molecular clone sequence data has been matched to the reference identifier above as a point of reference. Note that the complete sequence of our molecular clones may differ from the sequence published for this corresponding reference, e.g., by representing an alternative RNA splicing form or single nucleotide polymorphism (SNP). |
Reference Data | |
RefSeq | BC030295.2, AAH30295.1 |
RefSeq Size | 922 |
Locus ID | 155368 |
Gene Summary | This gene encodes a protein belonging to ubiE/COQ5 methyltransferase family. The gene is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.22-q11.23. [provided by RefSeq, Jul 2008] |
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