Lamin B Receptor (LBR) (NM_002296) Human 3' UTR Clone
CAT#: SC216584
3' UTR clone of lamin B receptor (LBR) transcript variant 1 for miRNA target validation
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CNY 5,795.00
货期*
3周
规格
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经常一起买 (2)
Specifications
Product Data | |
Product Name | Lamin B Receptor (LBR) (NM_002296) Human 3' UTR Clone |
Vector | pMirTarget |
Synonyms | C14SR; DHCR14B; LMN2R; PHA; PHASK; TDRD18 |
ACCN | NM_002296 |
Insert Size | 1831 bp |
Sequence Data |
>SC216584 3’UTR clone of NM_002296
The sequence shown below is from the reference sequence of NM_002296. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC CCCTACCGTATATTTCCATACATCTACTAATGCTCTTCTGGCTTTTCTACAAAATACTCCTGCAATTCC AGCTGCCATTTGCAAAAACAAGGAAAAAAATCCGAAACTTTCTTTTGTTGCACTGACAGGGTCTGTACT TTTTTTTTTCTTTTTGAGTCAGGACTATGGAGCCGAGTAGTTGATCTTTTAATATAGCCGTGTTTACTT GTATTAACTTACAGTTAACATAGGAAAAATACAAGTAAGGATGTGAGAATTTGCATTTTAATGGGAAAT TTTCAACCCTTAATCTGAAAACAGAAGACAGTCTTAATATAAATGTACTGTGAAGAATGCTATTGATGT TTATGGTTTCTGATTACTTTTCAAATTTTGATGTTTTTTTGCCAGTTGGCTTTTCTTAAATGAAAACAC TGTTCCATTTAAAGTACATTTATGTTTTATTCAGTAAGAGAATAGAATTTTCATTTGTTTTTCTTTAAA TCCTTTACTAATTATATAATTTGAAAGCAAAAAGAAGGGCCTATATTAAATGCTGAAAGTGAAAAGTGA TGACATTATTAGCAGACACTGCTTAAAGGAGACCATTTGTAGCAGTTGGCTTAACCTCAACTTCTAAAA CTACATTGAAAATGTAAATACATAGCTTAGTTTTTTGTAATATATGGTGACTTCAGATTTTTTTGTACA GTATTTTGAATGTGAGATGATTGTCAGGACTAACTGTCTTTTTAACAAAACATTTTCAGTATTTTAAAT AAAATTTTGTAAAGTAATGTGAATTAAAAATTTTGGAACAATTAGAATTCATTCACTATTGTATAGAAG ATGCTGTTAAAACATAGGAAGGGTATTTTTCTTGATCCAAAGTTTGTGAATTTGGCTTTGCTACCTCAA TTGCAGGTGTTTGTTTGCCTTTATAAACTGTTGCAAATAGAAAAAAAATAGAATAAGTATATATTTTTG GAGTAACATCAATATTTAAACATTTTTACACAGATCGGTGTTTGAAAATTTGCCATTTCAGGCTAATAT TTTTATATATTTTTGACTTTTTAAAAGTTCATCAGTGTTTTTGCTACTGTTAAGCTTATGCAGTTTATA CTGTATTTTTTATGTATCCTTTATATTTACCAAACCTGACTCCCTGTAAAGGAGTGCTGTCTTAAAAAC AACTGAAGGGGTTAAAGTCGTTTCTTTTAGTTTAATAGATGTGCATAAGGTAGCTTTAGCAATTAAATT CTAGTGAAGTTGATATAGTCTCATTTTTAATTGTCCTGTAATGGAACAGTAGCAAATTCACTAAACTTT TGTGTTCAGAGTTAAATTGTTCTCAGTACTTTCAATGTAGGGGAATGTAATAAACATAGTGTGTATGTT TGGGTTTTAATTACACATTTTATATATGAGCCATTTAGATATGCAGTGTTAATTCTATACTGCATTTGA AGTGTATGTAACTTAGCTTATGTTAATGCAGTCATGAAGTTGGTTTGCTCCAGCATCCGGTAGTCTTTA AACATTCTTTTAGTGAAATTGTCATTGTTTTATCAGTGCTAATGTGTGCAAGCAGTTTTTTTATTTTGC TTTTCTCCTGGCATCAGAAAGTGGTGGCGTTTTCTGTACTGGATTGCACCAAGGAAGCTTTTGGGGAGG AAGGAAGGACATTAAATTCTTTCCCTGGTAATGAAAAGAGCCCTTTATCAATACAGTGCTGCAATTTCT GGATATCAGCTACACTTTGTTTTTAAGTTTGTTTTTGACATGTTTATTTGGCAAATTTTATAATGAAGT TTTAAGTTGAAAATAAAATGTAGCAACATTTTGATCA ACGCGTAAGCGGCCGCGGCATCTAGATTCGAAGAAAATGACCGACCAAGCGACGCCCAACCTGCCATCA CGAGATTTCGATTCCACCGCCGCCTTCTATGAAAGG |
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_002296.4 |
Synonyms | C14SR; DHCR14B; LMN2R; PHA; PHASK; TDRD18 |
Summary | The protein encoded by this gene belongs to the ERG4/ERG24 family. It localized in the nuclear envelope inner membrane and anchors the lamina and the heterochromatin to the membrane. It may mediate interaction between chromatin and lamin B. Mutations of this gene has been associated with autosomal recessive HEM/Greenberg skeletal dysplasia. Alternative splicing occurs at this locus and two transcript variants encoding the same protein have been identified. [provided by RefSeq, Jul 2008] |
Locus ID | 3930 |
MW | 72.1 |
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