CHD8 (NM_020920) Human 3' UTR Clone

Specifications

Product Data
Product Name	CHD8 (NM_020920) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	AUTS18; HELSNF1
ACCN	NM_020920
Insert Size	444 bp
Sequence Data	Insert Sequence (showhide) >SC205971 3’UTR clone of NM_020920 The sequence shown below is from the reference sequence of NM_020920. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC TCAGACTCCAGTGAAGATGCTGATGACTGAAGCCCCAGCATGGGCCCCATTGCTTGGGCGGCTGCTGTA TTTTCATTTACTCTGGCCCTTGGACTATGGAAACGTGGGAGGGGCAGGGGAGATGTGGGGAAGTCCAGG ACTCCAGGAGGTGAAAAGGAAAAAAAAAAAAAAATGTACCTGATTGCTCCCAATTATGAGAGGATTGGG TGGGCAGGGGAACTCCTAAAATAATACATGACCACTTCCTCATTTCTGGGGAAGGAAAGGAGACTAGAG CAGCTGGTGTGCTCACCCCTCCCTAGTCACCTCCATTAACCACAGACTATGTAGCGCTGGCCCTAGCCT CTGGCAGAGCCTGTTCCTGGCCGAACTGTGGATACAGCTGGAGGGTCAGGAACTGTTACCTTCTTTCCC CTTGGCATTAATAAATTTAAGTTAATCCTT 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_020920.4
Synonyms	AUTS18; HELSNF1
Summary	This gene encodes a member of the chromodomain-helicase-DNA binding protein family, which is characterized by a SNF2-like domain and two chromatin organization modifier domains. The encoded protein also contains brahma and kismet domains, which are common to the subfamily of chromodomain-helicase-DNA binding proteins to which this protein belongs. This gene has been shown to function in several processes that include transcriptional regulation, epigenetic remodeling, promotion of cell proliferation, and regulation of RNA synthesis. Allelic variants of this gene are associated with autism spectrum disorder. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2016]
Locus ID	57680
MW	16.3

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