FXR2 (NM_004860) Human 3' UTR Clone

Specifications

Product Data
Product Name	FXR2 (NM_004860) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	FMR1L2; FXR2P
ACCN	NM_004860
Insert Size	630 bp
Sequence Data	Insert Sequence (showhide) >SC208279 3’UTR clone of NM_004860 The sequence shown below is from the reference sequence of NM_004860. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC TTGGGTAGTATGGTGAATGGGGTTTCATAAAACCTCCAACCTGCACCCCTCCCTTCTCCATCTCGCTTG CTGCCCAACACCATGGCCCTCACAGGCCCAACTGACCTGCGCTGGAGCTGCTCTTATCTAGGGGGGAGG GGGGTGGCACAGCAGCTTGGGTACCCCCCAACCTCCAGGAGCTAGTGGAGGGGTGTGTAACAGGGTCAT ACCCCCTCCCTCTTGTCCACCCTACCCCCAGGGTAAGGGGAGCCTCTCTCCTTCCCCATCAGACTGGAT GTGCCTTTATCCTCTAATGCCCCAATCTCTCTCTGAACACCCCCATTCTCCACCTGTTGGTGGGGGGTG CTCCTCGACCCACCCAGATTTGACCGTTCAGGGGGCCTCCCCTGCTATCCCTCCTCCCATCCTGTACCC CCCATTTCTGGGGCCTCATCACTGTGGAAGACGGGGATAGTAAGAGATAAGTGGGTGGGAGGCACGGGG AAGGTTTTGGAGTAGAACCAGGGGTGTGTATGAAGGGGGGTGACAAGGTCCCCCTGGGGAGGGGACCAA CCTTGTCTGGTGGATGAGAAGGCGTATTTATTTTTCACTGTACAGTATTTAAAAAGAGAATAAAAAAAT CCAAATGGC 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_004860.4
Synonyms	FMR1L2; FXR2P
Summary	The protein encoded by this gene is a RNA binding protein containing two KH domains and one RCG box, which is similar to FMRP and FXR1. It associates with polyribosomes, predominantly with 60S large ribosomal subunits. This encoded protein may self-associate or interact with FMRP and FXR1. It may have a role in the development of fragile X cognitive disability syndrome. [provided by RefSeq, Jul 2008]
Locus ID	9513
MW	22.6

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