TRIM37 (NM_001005207) Human 3' UTR Clone
CAT#: SC203664
3' UTR clone of tripartite motif-containing 37 (TRIM37) 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 | TRIM37 (NM_001005207) Human 3' UTR Clone |
Vector | pMirTarget |
Synonyms | MUL; POB1; TEF3 |
ACCN | NM_001005207 |
Insert Size | 299 bp |
Sequence Data |
>SC203664 3’UTR clone of NM_001005207
The sequence shown below is from the reference sequence of NM_001005207. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC TTCAATACAGATGAAAATAGTGGAAGATAATTTGATTTGAAACTGACACTGCACCTGATGGGTTAACAA GATCTAGGCTTCAGAAGGTGACAGATATGAGTGAGGACCATGTGTGGGGCAAAGCCTCAGAATGATGAA AAGGTTCCGGCACTATAGTTGGGGCCATGTTGACTCCTTTTCAACCATTTGTCACAGACGTGAGAAGAA GAAATGACTTCAAAATCAAGAGAAAACAAATACTGAAAGTCTCTACTTACATCCAAATTTTAAAAAATA AAATCTGTAGATTAACAATCTGA 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_001005207.5 |
Synonyms | MUL; POB1; TEF3 |
Summary | This gene encodes a member of the tripartite motif (TRIM) family, whose members are involved in diverse cellular functions such as developmental patterning and oncogenesis. The TRIM motif includes zinc-binding domains, a RING finger region, a B-box motif and a coiled-coil domain. The RING finger and B-box domains chelate zinc and might be involved in protein-protein and/or protein-nucleic acid interactions. Mutations in this gene are associated with mulibrey (muscle-liver-brain-eye) nanism, an autosomal recessive disorder that involves several tissues of mesodermal origin. TRIM37 localizes in peroxisomal membranes, and has been implicated in human peroxisomal biogenesis disorders. [provided by RefSeq, Jul 2020] |
Locus ID | 4591 |
MW | 11.4 |
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