Neurofibromin (NF1) (NM_001128147) Human 3' UTR Clone

Specifications

Product Data
Product Name	Neurofibromin (NF1) (NM_001128147) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	NFNS; VRNF; WSS
ACCN	NM_001128147
Insert Size	804 bp
Sequence Data	Insert Sequence (showhide) >SC209754 3’UTR clone of NM_001128147 The sequence shown below is from the reference sequence of NM_001128147. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC TTTAAATTTTATTTTGTATTTTTGTCTTGAAATATTAACTCTGTAGTACTTAGTACATTGTAAAACTTA CACTTCCAAAGGTTTTATGGTTTTGTATTTTATTTGACTTCAAATTATTAGAATTTCTTGTTTTAACTG TAAGAAAAGTATCACAGCAATTTAGAAAATAAATTTTAAGAATAGTGCTAAATTTTGTCACCCTAACAT AAGTACTGTTGTTTGGTATATTACTTTTTTCAGATTTCAATGTGGTTACTACTGTATTTTTAATAGATT TTCATAGTTATAAGCCTAGAATGATAAAATTTTGTAACAATACTGTTTTTTCAGTTTTTTGAACTATGA TCTTTCATAAACTTTCTGTAATACCAATGCTTTCGATGAATGAATTAATAATGGACACCTGCTTAGAAG AAAAAAATGTATGCAGAATTTTGTGGTCTGCTTCCTAGATTATACAAATCATTACATTTTAATGAGCAT GAAGTCACCACACGGAGGAAAATGTAAATGTGTAAACCTCAAGTTTGCCATTATCTTATAAGAATGGGT GTGCTAAGTTACTTGGCAGCTGAATTAAACCTTACTCTAGAGTAGTGCTGTCCACTAGTAATATAATGA GAACCCCATATGTTAAAAACTTTTTTACTTACTACATTAAAGAGTAAAAAGAAGCAGGTAAAATTAATT GTAATTATGTTTTGTTTAACCCGGTGTATATTATCTATAATTTCAACATGTAATCAATATAAAAGTTAT TAATGACATTTCATTCTCTTTTTTTTAATAAAGTCTTCAAACTTT 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_001128147.3
Synonyms	NFNS; VRNF; WSS
Summary	This gene product appears to function as a negative regulator of the ras signal transduction pathway. Mutations in this gene have been linked to neurofibromatosis type 1, juvenile myelomonocytic leukemia and Watson syndrome. The mRNA for this gene is subject to RNA editing (CGA>UGA->Arg1306Term) resulting in premature translation termination. Alternatively spliced transcript variants encoding different isoforms have also been described for this gene. [provided by RefSeq, Jul 2008]
Locus ID	4763
MW	32.4

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