CHREBP (MLXIPL) (BC012925) Human Untagged Clone
CAT#: SC126048
MLXIPL (untagged)-Human Williams Beuren syndrome chromosome region 14, mRNA (cDNA clone MGC:9556 IMAGE:3866131), complete cds
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Specifications
Product Data | |
Type | Human Untagged Clone |
Tag | Tag Free |
Symbol | MLXIPL |
Synonyms | bHLHd14; carbohy; carbohydrate response element binding protein; CHREBP; MIO; Mlx interactor; MONDOB; OTTHUMP00000160457; OTTHUMP00000160458; WBSCR14; Williams Beuren syndrome chromosome region 14; WS-bHLH; WS basic-helix-loop-helix leucine zipper protein |
Vector | pCMV6-XL5 |
E. coli Selection | Ampicillin (100 ug/mL) |
Mammalian Cell Selection | None |
Sequence Data |
>OriGene sequence for BC012925 edited
GGCGGTTGCGGCGGCGACAGCCATGGCCGGCGCGCTGGCAGGTCTGGCCGCGGGCTTGCA GGTCCCGCGGGTCGCGCCCAGCCCAGACTCGGACTCGGACACAGACTCGGAGGACCCGAG TCTCCGGCGCAGCGCGGGCGGCTTGCTCCGCTCGCAGGTCATCCACAGCGGTCACTTCAT GGTGTCGTCGCCGCACAGCGACTCGCTGCCCCGGCGGCGCGACCAGGAGGGGTCCGTGGG GCCCTCCGACTTCGGGCCGCGCAGTATCGACCCCACACTCACACGCCTCTTCGAGTGCTT GAGCCTGGCCTACAGTGGCAAGCTGGTGTCTCCCAAGTGGAAGAATTTCAAAGGCCTCAA GCTGCTCTGCAGAGACAAGATCCGCCTGAACAACGCCATCTGGAGGGCCTGGTATATCCA GTATGTGAAGCGGAGGAAGAGCCCCGTGTGTGGCTTCGTGACCCCCCTGCAGGGGCCTGA GGCTGATGCGCACCGGAAGCCGGAGGCCGTGGTCCTGGAGGGGAACTACTGGAAGCGGCG CATCGAGCTGCCGCCTGAGGATGCCTACGTCGGCAATGCTGACATGATCCAGCCGGACCT GACGCCACTGCAGCCAAGCCTGGATGACTTCATGGACATCTCAGATTTCTTTACCAACTC CCGCCTCCCACAGCCGCCCATGCCTTCAAACTTCCCAGAGCCCCCCAGCTTCAGCCCCGT GGTTGACTCCCTCTTCAGCAGTGGGACCCTGGGCCCAGAGGTGCCCCCGGCTTCCTCGGC CATGACCCACCTCTCTGGACACAGCCGTCTGCAGGCTCGGAACAGCTGCCCTGGCCCCTT GGACTCCAGCGCCTTCCTGAGTTCTGATTTCCTCCTTCCTGAAGACCCCAAGCCCCGGCT CCCACCCCCTCCTGTACCCCCACCTCTGCTGCATTACCCTCCCCCTGCCAAGGTGCCAGG CCTGGAGCCCTGCCCCCCACCTCCCTTCCCTCCCATGGCACCACCCACTGCTTTGCTGCA GGAAGAGCCTCTCTTCTCTCCCAGGTTTCCCTTCCCCACCGTCCCTCCTGCCCCAGGAGT GTCTCCGCTGCCTGCTCCTGCAGCCTTCCCACCCACCCCACAGTCTGTCCCCAGCCCAGC CCCCACCCCCTTCCCCATAGAGCTTCTACCCTTGGGGTATTCGGAGCCTGCCTTTGGGCC TTGCTTCTCCATGCCCAGAGGCAAGCCCCCCGCCCCATCCCCTAGGGGACAGAAAGCCAG CCCCCCTACCTTAGCCCCTGCCACTGCCAGTCCCCCCACCACTGCGGGGAGCAACAACCC CTGCCTCACACAGCTGCTCACAGCAGCTAAGCCGGAGCAAGCCCTGGAGCCACCACTTGT ATCCAGCACCCTCCTCCGGTCCCCAGGGTCCCCGGAGACAGTCCCTGAATTCCCCTGCAC ATTCCTTCCCCCGACCCCGGCCCCTACACCGCCCCGGCCACCTCCAGGCCCGGCCACATT GGCCCCTTCCAGGCCCCTGCTTGTCCCCAAAGCGGAGCGGCTCTCACCCCCAGCGCCCAG CGGCAGTGAACGGCGGCTGTCAGGGGACCTCAGCTCCATGCCAGGCCCTGGGACTCTGAG CGTCCGTGTCTCTCCCCCGCAACCCATCCTCAGCCGGGGCCGTCCAGACAGCAACAAGAC CGAGAACCGGCGTATCACACACATCTCCGCGGAGCAGAAGCGGCGCTTCAACATCAAGCT GGGGTTTGACACCCTTCATGGGCTCGTGAGCACACTCAGTGCCCAGCCCAGCCTCAAGGT GAGCAAAGCTACCACGCTGCAGAAGACAGCTGAGTACATCCTTATGCTACAGCAGGAGCG TGCGGGCTTGCAGGAGGAGGCCCAGCAGCTGCGGGATGAGATTGAGGAGCTCAATGCCGC CATTAACCTGTGCCAGCAGCAGCTGCCCGCCACAGGGGTACCCATCACACACCAGCGTTT TGACCAGATGCGAGACATGTTTGATGACTACGTCCGAACCCGTACGCTGCACAACTGGAA GTTCTGGGTGTTCAGCATCCTCATCCGGCCTCTGTTTGAGTCCTTCAACGGGATGGTGTC CACGGCAAGTGTGCACACCCTCCGCCAGACCTCACTGGCCTGGCTGGACCAGTACTGCTC TCTGCCCGCTCTCCGGCCAAGTACGTGAGCCATCTCCCTGCCTGCTAGAGGGACCCAGCC TCGGGGGTGGAGGGAGCATTCCACCCTGCTTAGATCCCACATCCAGCTTGCCATCAACAC AGCCTAGGGTTGTGGCCACCCCGCATCCCCCAGATGGTCCTCTGGCCACCAGACGCCTGT AGACAGAGGTTCTAGGAGGGGGTGACAGTCTTGCCAACTAATACCTCCCCCTATCCCTTT GGTTCCACATCCAAGGGTAGGGCCCTGACCCCAGGAAGTGTCTGTCTCTCTCTCTCTGTC TCCCACCCAGCTGTCCTGAACTCCCTACGCCAGCTGGGCACATCTACCAGTATCCTGACC GACCCGGGCCGCATCCCTGAGCAAGCCACACGGGCAGTCACAGAGGGCACCCTTGGCAAA CCTTTATAGTCCTGGCCAGACCCTGCTGCTCACTCAGCTGCCCTGGGGGCTGCTTTCCCT GGGCACGGGCTCCAGGGATCATCTCTGGGCACTCCCTTCCTGCCCCAGGCCCTGGCTCTG CCCTTCCCTGGGGGGTGGAGCAGGGTCCAGGTTTCACACTTGCCACCTCCTGGAGGTCAA GAAGAGCAGAGTCCCCGTCCCTGCTCTGCCACTGTGCTCCAGCACCGTGACCTTGGGTGA CTCGTCCGCTGTCTTTGGACCGCTGTGTTTCAATCTGCAAAATGGGGATGGGGAAGGTTC AATCAGCAGATGACCCCCAGGCCTTGGCAGCTGTGACATTGGGGGCCTAGGCTGGCAACT CCGGGGGCTCAACGGTGGAAAGAGGAGGATGCTGTTTCTCTGTCACCTCCACTTGCTCCC CGACAGGTGGGGCACAGACCTCTGTTCCTGAGCAGAGAAGCAGAAAAGGAGGTTCCCTCT CTCTGCTCCTTCACTGCTGACCCAGAGGGGCTGCAGGATGGTTTCCCCTGGGAGAGGCCA GGAGGGCCTGATCCCAGGAGACACCAGGGCCAGAGTGACCACAGCAGGGCAGGCATCATG TGTGTGTGTGTGTGTGGATGTGTGTGTGTGGGTTTTGTAAAGAATTCTTGACCAATAAAA GCAAAAACTGTCAAAAAAAAAAAAAAA >OriGene 5' read for BC012925 unedited
NGGGAGTTCTGATTTGTATACCATTATATAGGCGGCCGCGNATTCAAATCTGGTACCGGT CCGGAATTCCCGGGNAATCGTCGACCCACGCGTCCGGGCGGTTGCGGCGGCGACAGCCAT GGCCGGCGCGCTGGCAGGTCTGGCCGCGGGCTTGCAGGTCCCGCGGGTCGCGCCCAGCCC AGACTCGGACTCGGACACAGACTCGGAGGACCCGAGTCTCCGGCGCAGCGCGGGCGGCTT GCTCCGCTCGCAGGTCATCCACAGCGGTCACTTCATGGTGTCGTCGCCGCACAGCGACTC GCTGCCCCGGCGGCGCGACCAGGAGGGGTCCGTGGGGCCCTCCGACTTCGGGCCGCGCAG TATCGACCCCACACTCACACGCCTCTTCGAGTGCTTGAGCCTGGCCTACAGTGGCAAGCT GGTGTCTCCCAAGTGGAAGAATTTCAAAGGCCTCAAGCTGCTCTGCAGAGACAAGATCCG CCTGAACAACGCCATCTGGAGGGCCTGGTATATCCAGTATGTGAAGCGGAGGAAGAGCCC CGTGTGTGGCTTCGTGACCCCCCTGCAGGGGCCTGAGGCTGATGCGCACCGGAAGCCGGA GGCCGTGGTCCTGGAGGGGAACTACTGGAAGCGGCGCATCGAGCTGCCGCCTGAGGATGC CTACGTCGGCAATGCTGACATGATCCAGCCGGACCTGACGCCACTGCAGCCAAGCCTGGA TGACTTCATGGACATCTCAGATTTCTTTACCAACTCCCGCCTCCCAAGCCGCCCATGCCT TCAAACTTCCCAGAGCCCCCCAGCTTCAGCCCCGTGGTTGACTCCCTCTTCAGCAGTGGG ACCCTGGGCCCAN |
Restriction Sites | NotI-NotI |
ACCN | BC012925 |
Insert Size | 3300 |
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). |
OTI Annotation | This TrueClone is provided through our Custom Cloning Process that includes sub-cloning into OriGene's pCMV6 vector and full sequencing to provide a non-variant match to the expected reference without frameshifts, and is delivered as lyophilized plasmid DNA. |
Reference Data | |
RefSeq | BC012925.1, AAH12925.1 |
RefSeq Size | 3267 |
Locus ID | 51085 |
Gene Summary | This gene encodes a basic helix-loop-helix leucine zipper transcription factor of the Myc/Max/Mad superfamily. This protein forms a heterodimeric complex and binds and activates, in a glucose-dependent manner, carbohydrate response element (ChoRE) motifs in the promoters of triglyceride synthesis genes. The gene is deleted in Williams-Beuren syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at chromosome 7q11.23. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2015] |
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