LEPRE1 (P3H1) (NM_001146289) Human 3' UTR Clone
CAT#: SC206858
3' UTR clone of leucine proline-enriched proteoglycan (leprecan) 1 (LEPRE1) transcript variant 2 for miRNA target validation
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CNY 4,845.00
货期*
3周
规格
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经常一起买 (2)
Specifications
Product Data | |
Product Name | LEPRE1 (P3H1) (NM_001146289) Human 3' UTR Clone |
Vector | pMirTarget |
Synonyms | GROS1; LEPRE1; OI8 |
ACCN | NM_001146289 |
Insert Size | 489 bp |
Sequence Data |
>SC206858 3’UTR clone of NM_001146289
The sequence shown below is from the reference sequence of NM_001146289. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC GCTCGAGCGGGACAGGGTGCAGGCAGATGACCTGGTGAAGATGCTCTTCAGCCCAGAAGAGATGGACCT CTCCCAGGAGCAGCCCCTGGATGCCCAGCAGGGCCCCCCCGAACCTGCACAAGAGTCTCTCTCAGGCAG TGAATCGAAGCCCAAGGATGAGCTATGACAGCGTCCAGGTCAGACGGATGGGTGACTAGACCCATGGAG AGGAACTCTTCTGCACTCTGAGCTGGCCAGCCCCTCGGGGCTGCAGAGCAGTGAGCCTACATCTGCCAC TCAGCCGAGGGGACCCTGCTCACAGCCTTCTACATGGTGCTACTGCTCTTGGAGTGGACATGACCAGAC ACCGCACCCCCTGGATCTGGCTGAGGGCTCAGGACACAGGCCCAGCCACCCCCAGGGGCCTCCACAGGC CGCTGCATGACAGCGATACAGTACTTAAGTGTCTGTGTAGACAACCAAAGAATAAATGATTCATGGTTT TTTTTA 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_001146289.2 |
Synonyms | GROS1; LEPRE1; OI8 |
Summary | This gene encodes an enzyme that is a member of the collagen prolyl hydroxylase family. These enzymes are localized to the endoplasmic reticulum and their activity is required for proper collagen synthesis and assembly. Mutations in this gene are associated with osteogenesis imperfecta type VIII. Three alternatively spliced transcript variants encoding different isoforms have been described. Other variants may exist, but their biological validity has not been determined. [provided by RefSeq, Aug 2011] |
Locus ID | 64175 |
MW | 17.2 |
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