MERTK (NM_006343) Human 3' UTR Clone

Specifications

Product Data
Product Name	MERTK (NM_006343) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	c-Eyk; c-mer; MER; RP38; Tyro12
ACCN	NM_006343
Insert Size	727 bp
Sequence Data	Insert Sequence (showhide) >SC206879 3’UTR clone of NM_006343 The sequence shown below is from the reference sequence of NM_006343. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC TCCTCAGAAGGCTCAGAAGTCCTGATGTGAGGAGAGGTGCGGGGAGACATTCCAAAAATCAAGCCAATT CTTCTGCTGTAGGAGAATCCAATTGTACCTGATGTTTTTGGTATTTGTCTTCCTTACCAAGTGAACTCC ATGGCCCCAAAGCACCAGATGAATGTTGTTAAGTAAGCTGTCATTAAAAATACATAATATATATTTATT TAAAGAGAAAAAATATGTGTATATCATGGAAAAAGACAAGGATATTTTAATAAAACATTACTTATTTCA TTTCACTTATCTTGCATATCTTAAAATTAAGCTTCAGCTGCTCCTTGATATTAACATTTGTACAGAGTT GAAGTTGTTTTTTCAAGTTCTTTTCTTTTTCATGACTATTAAATGTAAAAATATTTGTAAAATGAAATG CCATATTTGACTTGGCTTCTGGTCTTGATGTATTTGATAAGAATGATTCATTCAATGTTTAAAGTTGTA TAACTGATTAATTTTCTGATATGGCTTCCTAATAAAATATGAATAAGGAAGGATATGTTGAACTTACTT GAGACTTGAAAGACAGTGGTCGGCAGCGGCCTTGTGGCCTTTGCAAAGGAATTCCCTTAATGCCTGGTC CTTGGGGCAATTGCTCTGACCATTCTTGGCATTGCTTTATAGAGATATGGAAAAACCACACCAGGGTCT GTAGATAAGGAATAAAGAATATTGAAGGATTGAAAAA 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_006343.3
Synonyms	c-Eyk; c-mer; MER; RP38; Tyro12
Summary	This gene is a member of the MER/AXL/TYRO3 receptor kinase family and encodes a transmembrane protein with two fibronectin type-III domains, two Ig-like C2-type (immunoglobulin-like) domains, and one tyrosine kinase domain. Mutations in this gene have been associated with disruption of the retinal pigment epithelium (RPE) phagocytosis pathway and onset of autosomal recessive retinitis pigmentosa (RP). [provided by RefSeq, Jul 2008]
Locus ID	10461
MW	27.7

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