LMNB1 (NM_005573) Human 3' UTR Clone
CAT#: SC209554
3' UTR clone of lamin B1 (LMNB1) for miRNA target validation
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CNY 5464.00
货期*
现货
规格
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Specifications
| Product Data | |
| Product Name | LMNB1 (NM_005573) Human 3' UTR Clone |
| Vector | pMirTarget |
| Synonyms | ADLD; LMN; LMN2; LMNB; MCPH26 |
| ACCN | NM_005573 |
| Insert Size | 775 bp |
| Sequence Data |
>SC209554 3' UTR clone of NM_005573
The sequence shown below is from the reference sequence of NM_005573. The complete sequence of this clone may contain minor differences, such as SNPs. Red=Cloning site Blue=Stop Codon CAATTGGCAGAGCTCAGAATTCAAGCGATCGC GCATCCAATAGAAGCTGTGCAATTATGTAAAATTTTCAACTGTCTTCCTCAAAATAAAGAAGTATGGTAA TCCTTACCTGTATACAGTGCAGAGCCTTCTCAGAAGCACAGAATATTTTTATATTTCCTTTATGTGAATT TTTAAGCTGCAAATCTGATGGCCTTAATTTCCTTTTTGACACTGAAAGTTTTGTAAAAGAAATCATGTCC ATACACTTTGTTGCAAGATGTGAATTATTGACACTGAACTTAATAACTGTGTACTGTTCGGAAGGGGTTC CTCAAATTTTTTGACTTTTTTTGTATGTGTGTTTTTTCTTTTTTTTTAAGTTCTTATGAGGAGGGGAGGG TAAATAAACCACTGTGCGTCTTGGTGTAATTTGAAGATTGCCCCATCTAGACTAGCAATCTCTTCATTAT TCTCTGCTATATATAAAACGGTGCTGTGAGGGAGGGGAAAAGCATTTTTCAATATATTGAACTTTTGTAC TGAATTTTTTTGTAATAAGCAATCAAGGTTATAATTTTTTTTAAAATAGAAATTTTGTAAGAAGGCAATA TTAACCTAATCACCATGTAAGCACTCTGGATGATGGATTCCACAAAACTTGGTTTTATGGTTACTTCTTC TCTTAGATTCTTAATTCATGAGGAGGGTGGGGGAGGGAGGTGGAGGGAGGGAAGGGTTTCTCTATTAAAA TGCATTCGTTGTGTTTTTTAAGATAGTGTAACTTGCTTAAATTTCTTATGTGACATTAACAAATAAAAAA GCTCT ACGCGTAAGCGGCCGCGGCATCTAGATTCGAAGAAAATGACCG |
| Restriction Sites | SgfI-MluI |
| OTI Disclaimer | Our molecular clone sequence data has been matched to the sequence identifier above as a point of reference. Note that the complete sequence of this clone is largely the same as the reference sequence but may contain minor differences , e.g., single nucleotide polymorphisms (SNPs). |
| Reference Data | |
| RefSeq | NM_005573.2 |
| Synonyms | ADLD; LMN; LMN2; LMNB; MCPH26 |
| Summary | This gene encodes one of the two B-type lamin proteins and is a component of the nuclear lamina. A duplication of this gene is associated with autosomal dominant adult-onset leukodystrophy (ADLD). Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2015] |
| Locus ID | 4001 |
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