Neurofilament (NEFM) (NM_001105541) Human 3' UTR Clone

Specifications

Product Data
Product Name	Neurofilament (NEFM) (NM_001105541) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	NEF3; NF-M; NFM
ACCN	NM_001105541
Insert Size	517 bp
Sequence Data	Insert Sequence (showhide) >SC206570 3’UTR clone of NM_001105541 The sequence shown below is from the reference sequence of NM_001105541. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC ATAGTAAAGGAAGTCACCCAGAGTGACTAAGATTTGAGTCCATTGCAAAAGGTTAAGCCATATGACAAT TTCAAAATGCATGTGATTGGCAGCTTCAAAACAGAACGGGTTCTCCCATGGGGGCTCCAGACATTGTAT TTTACTTTGTGCAATATGAGGGGACTGCATGCAAGCTCAGGGTGCTCCCTCCTCAGTCTTTGGGGGATT CAAATGCATGATATTGTATGTACCTGGGAAATTTGCCGATTTCCTAAGCTGTTGGAAGGGGGTCACTTA AGGGGGGATGTCTTGAGATGTATTATGCAAAGTACCAACTGAGCCAAAAACAATAAACGAAACACAGAA CTCAGCCTTAAGAAAGCTATATATGAATAATTATGTTTACCTCACTGGTGCATTTAAAATGGACTTTTG TTCATGGGAGAACCTCGTTGACATGCACAGTTTGCAATCTTATGTTGATCGATGTTAAACGTCACAGCA GTACTTGCTCAATAAAGGTCATATTGGAAACATA 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_001105541.2
Synonyms	NEF3; NF-M; NFM
Summary	Neurofilaments are type IV intermediate filament heteropolymers composed of light, medium, and heavy chains. Neurofilaments comprise the axoskeleton and functionally maintain neuronal caliber. They may also play a role in intracellular transport to axons and dendrites. This gene encodes the medium neurofilament protein. This protein is commonly used as a biomarker of neuronal damage. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Oct 2008]
Locus ID	4741
MW	19.8

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