SMARCAL1 (NM_001127207) Human 3' UTR Clone

Specifications

Product Data
Product Name	SMARCAL1 (NM_001127207) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	HARP; HHARP
ACCN	NM_001127207
Insert Size	106 bp
Sequence Data	Insert Sequence (showhide) >SC200428 3’UTR clone of NM_001127207 The sequence shown below is from the reference sequence of NM_001127207. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC AACTGGGACAGCTTTACGTCTCCCCTGTAAAAGGGGCAAAAAGAAAAAAATAAAAAGCATTTTAAAATC ATGGAATTGAAATAAAATAATGTATTTTGTTTTAAAA 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_001127207.2
Synonyms	HARP; HHARP
Summary	The protein encoded by this gene is a member of the SWI/SNF family of proteins. Members of this family have helicase and ATPase activities and are thought to regulate transcription of certain genes by altering the chromatin structure around those genes. The encoded protein shows sequence similarity to the E. coli RNA polymerase-binding protein HepA. Mutations in this gene are a cause of Schimke immunoosseous dysplasia (SIOD), an autosomal recessive disorder with the diagnostic features of spondyloepiphyseal dysplasia, renal dysfunction, and T-cell immunodeficiency. [provided by RefSeq, Jul 2008]
Locus ID	50485
MW	4.3

*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.