SOX18 (NM_018419) Human 3' UTR Clone

Specifications

Product Data
Product Name	SOX18 (NM_018419) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	HLTRS; HLTS
ACCN	NM_018419
Insert Size	614 bp
Sequence Data	Insert Sequence (showhide) >SC206116 3’UTR clone of NM_018419 The sequence shown below is from the reference sequence of NM_018419. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC GTCTATTACAGCGCGTGCATCTCCGGCTAGGCCGCCGGCGCCGCCCGGGTCCCTGCAGCGCTTCCTCCC GCAGCCCCCGCGACCGATCCGACCGCGTCGCTGCCGCTCTGCTCTCTCATACGCGTGTATGTTTGGTTC CATGTCACAGCCCCCTAGGAGCCAGTGATGCTCGGCCTTGCGCCCGTTCCACCTCCCAGGCCACCCTTC CTGGGCTTCTGGGCCACCTGCCCTCGGGGGGCCCCTGCGAGGGTGCCTGGAGTTCCCACGTGTCCCGGG GCTTTTCCAGGAAGCCCGAGCCCAGGACCTGTTGGCAGAGTTGCCAGGGTTACATTTTTGAAGCACCTG CTCCTTTTCTTGCAGTGTATTTTCTACAACCAGATTGTATTAATATTTTTTACTTTGCCCTTTTAAAAA ATATACCTAATACAATATATTTAATTTTTAATTAAACTCTTAAACTTTTCTTCCAAGAAGTTTCAGTGA TCAGAAGCGTCACTGTGGCAAAGACTTTTGCAATGTGAGGAATACAGATGTTTGCTTTCTATAAAGGAG GAGCCTGGAGCTGGGTCCCCGGACGGAGAGGCCACAATAAATCCTCGGGCCTTTCCTCTGCA AGCGGACCGACTTACGCGTAAGCGGCCGCGGCATCTAGATTCGAAGAAAATGACCGACCAAGCGACGCC CAACCTGCCATCACGAGATTTCGATTCCACCGCCGC
Restriction Sites	SgfI-RsrII
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_018419.3
Synonyms	HLTRS; HLTS
Summary	This gene encodes a member of the SOX (SRY-related HMG-box) family of transcription factors involved in the regulation of embryonic development and in the determination of the cell fate. The encoded protein may act as a transcriptional regulator after forming a protein complex with other proteins. This protein plays a role in hair, blood vessel, and lymphatic vessel development. Mutations in this gene have been associated with recessive and dominant forms of hypotrichosis-lymphedema-telangiectasia. [provided by RefSeq, Jul 2008]
Locus ID	54345
MW	22.2

*Delivery time may vary from web posted schedule. Occasional delays may occur due to unforeseen complexities in the preparation of your product. International customers may expect an additional 1-2 weeks in shipping.