PQBP1 (NM_001032384) Human 3' UTR Clone

Specifications

Product Data
Product Name	PQBP1 (NM_001032384) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	MRX2; MRX55; MRXS3; MRXS8; NPW38; RENS1; SHS
ACCN	NM_001032384
Insert Size	125 bp
Sequence Data	Insert Sequence (showhide) >SC200541 3’UTR clone of NM_001032384 The sequence shown below is from the reference sequence of NM_001032384. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC GAGGCCTCCCGAACCAAGCAGCAGGATTGAAGCTTCGGCCTCCCTGGCCCTGGGTTAAAATAAAAGCTT TCTGGTGATCCTGCCCACCAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA 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_001032384.1
Synonyms	MRX2; MRX55; MRXS3; MRXS8; NPW38; RENS1; SHS
Summary	This gene encodes a nuclear polyglutamine-binding protein that is involved with transcription activation. The encoded protein contains a WW domain. Mutations in this gene have been found in patients with Renpenning syndrome 1 and other syndromes with X-linked cognitive disability. Multiple alternatively spliced transcript variants that encode different protein isoforms have been described for this gene.[provided by RefSeq, Nov 2009]
Locus ID	10084
MW	4.6

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