CFAP418 (NM_177965) Human 3' UTR Clone

Specifications

Product Data
Product Name	CFAP418 (NM_177965) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	BBS21; C8orf37; CORD16; FAP418; MOT25; RP64; smalltalk
ACCN	NM_177965
Insert Size	2000 bp
Sequence Data	Insert Sequence (showhide) >SC215600 3’UTR clone of NM_177965 The sequence shown below is from the reference sequence of NM_177965. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC CAGCTTCGCTGGGTTTGTGGTAAACATTAAGAATGCAGACTGCACATTCGGACAGATGCATCCATGAGA GTGGTCTCCATGAATCATCATCATGTTTAGACAATAGTCCCTAGCAATACCATTCCCTGTGGGAAAAGG CAGTGAATTTTATTGATACAACTACATACATTTTTGAAGACCAAATGGACTAAGGAAGATCATGTATTA TAACACTTTGGAATTATTCCTGATACATGGATGTTTCACTTAGTAACAGGCATCTACATTCTTTACTAA TCTGTCTTCTGTTTAATAGAGGTTTGATTATGGAGTTCCATACAAATATCTAGTTTTTCATTAGCAACT GCAATATTGATTGCTAATACGTTTAGCAAATCATTCCCCAACTTGTAGCAGTTAAAGTGGATAAAGCCG GCCAGGGCAAAGAGATCATTTAGGGGTGTCTACAACACTTCTTCCAGTCAGATCTTTTGTTGCCAAAGA TCATAATTTGGACATGGCAGAAACCAGGTGATCAGTGGCTGACTGAAGGGTGTTCAGAAGTAGTTACAG GTATTTTGCAAAAACACTGCCTCATAGCTGATCTTACCTCATCAACTCAAAGCAATGTTATGCACAATA TTAAATACATGTTACCAGTTTTAGCTTATTTTTCCCTCTTTTGTTCATTTAACTATCAAAAGTTATTTT CTATTTTGATTACCCAATAATATATAAAAAGAGTTTGATGCACCCAAAATCACAAAAATCCTAATACAT ACAGGTTATTGTTGGATTTTCCAAGTACTTTCTATCCTTTAATGCCTAAAACTCCATCAAGGGAAGTAA ACAGCAAGTAATATAATTTTTCAGGCAGCCTGTGGACTTCTCTGGTAGGATCAGGTTGACATATCGTTT ATTAGGTGAGTAAGTGAAAAGACAAGTAAAGCATAACTGAACCAACAGGTAACCTGTTGGGCTCCTTCC TGACATCACTGAGATCTGAGGAGCCCTACAATAGCAGCACATTCAGGAAATCAGGTCCCTCAAAATTTC TAGCTCCCAACCCCATTGAGAGATTTTGGGAGCTTTCCAATCTGCCACAAACTCCCTGCTACATATGTA CTATATAGTTCAAATGTGTGATACAGAGCACCCTGAAAGGGAATAATTGAAACAAAGTTATAATCTTCT TAGTCTTATGCTAAATTTATTCCAGCCACCCTACTGAAGGGAGGAAGATCTGATCATTAGAATCCTTTT CCTAGCCATGACACATTTACATACTTGTAAAATTTATTGTAGTAAGTCTAGCATTGCAACAGAATAGAT CTTATAATGGCCAATCCTCACACTTTTGTATTAAGGATATTATGACAGACTAAGCATGGTAGCTCACGC CTGTAATCCCAGCACTTTGGGAGGCTGAGGCAGGCAGATCAGCTGAGGTCAGGAGTTCAAGACCAGCCT GGCCAACATGATAAAACACCATCTCTACTAAAAATACAAAAATTAGCTGGGCGCGGTGGTGCATGCCTG TAATCCCAACTACTCGGGAGGCCGAGGCAGGAAAATTTATTGAACCTGGGAGGCAGAGGTTGTAGTGAG CCAAGGTCGCGCCACTGCGCTCCAGCCTGGACAACACAGTGAGACTCTGTCTCAAAAAAAAAAAAAAGA CATTATGACAGATTTTATCTTTTAATAAAAATGTATTATATCCCTAAAGTTATATCTATATGTAATTGA GTCAGAAACCTAGGGGGATGTCGATTGAAGTCGACTGCTGGAAAAAAATAGCAGAGCAACAAGATCCAC ACATTTAGAACCTCATAGAATTTGACACATTATTCATAATGGTGCAATTCTTTCTTTTTTATTCCAGTA AGCAAATTTACTAAATCACTAATTTGAAAAAAAAAATTTTTTTTTTGAGATGGAGTGTCACTCTGTTGC CGGGCTGGAGTGCAGTGGCACGATCTCTGCTCACTGCAACCTCCGCCTCGCAGCTTCAAGTGATTGTC 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_177965.4
Synonyms	BBS21; C8orf37; CORD16; FAP418; MOT25; RP64; smalltalk
Summary	This gene encodes a ubiquitously expressed protein of unknown function. It has high levels of mRNA expression in the brain, heart, and retina and the protein co-localizes with polyglutamylated tubulin at the base of the primary cilium in human retinal pigment epithelial cells. Mutations in this gene have been associated with autosomal recessive cone-rod dystrophy (arCRD) and retinitis pigmentosa (arRP). [provided by RefSeq, Mar 2012]
Locus ID	157657
MW	76.1

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