GLRB (NM_001166060) Human 3' UTR Clone

Specifications

Product Data
Product Name	GLRB (NM_001166060) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	HKPX2
ACCN	NM_001166060
Insert Size	1392 bp
Sequence Data	Insert Sequence (showhide) >SC214261 3’UTR clone of NM_001166060 The sequence shown below is from the reference sequence of NM_001166060. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC AATGTTATATATTGGTCTATATATTTATGATAAATCTTTTCCATTTGTACAAAATAAAATTCCATTTCA TTGTGACCTACTCCTTTCATAAATGCCAATCTGTGAGAACTTTTGAATTTTCATAGCAACATTGCATTT TGGATGCCATTTGATTGTAATAAAACTGTGGCACCTTAATTTTGAATGGCAGCATGATCATGTAATATC TGTGCTCTAATAACGATGTATATATGTATAGTGAACATATTGCTTAGTAACAAATGAAGGACAAGCATA CTACATAATATAATCCATACAATTCTCTTCAGTTAGTGTAAACTGCAAATACTACAGATAATTCTGATA ATAAAATGATATGCACGCTGAATCCTGCTATGGTCACCATTCTAATGTATGTAGTATTTCAAATTTCCT TCCTTGTAACTTTCAAAGAAAGCCATCTTATTCTTGTAAAATTTTAGATGGTATTATCACAGATTTAAA AAGGTTGTATTACATATTGTTTAAACTTTGTAAGTAGAAATATATCTGTTATAATTATACAGGCTCTGT GGAGAAATAAAGTTCAAAATATATTAATTTGTAAAATCAGCTCGTTTTAAAGTGTGCTTGTGTTGTCAA AAATATCAGATAGTAATACACAGTGAGCATTTTTAAACAAAGGGAAACCTATATTTATGTAACTGTATA CTGAATTCTGACAAAATAAAAAAAGATACCTTATTGACGAAATATTTAGGATAAACAAAATTCTATTTA ATCCACCTTAAAACCTAAATGTATTTTCATGGATTTCATTTGTTGGTACATATTACACAAAACATTGTG CCTTAAAATGAGTCATACATCTTTTAAATTGGAATGCAGTAATAGATATGTGATTTTACATCATTTTTA AGAAACCAAGGGGAAGTAATAAGTTGAAAAAGAAATCCATAACTATTAAAAGATTTTAACTTTTTTATT TTATTAAAATGCTTGCATATTTTAAGTAAAATTAAAAATGTTTACTGAATTTATTTTTTTATTTGAATA TTTTGGGATTAGTTACAAAATATTTAGAGATTAAATAAATAATAGCTTTGTTTGTGTTAGACTTCACTT CTACTTGTATTTTCTTTCTTGTTAAAAGTCTAGACAACTGAGATTTACTTACTTTGAACTTGTTCCAAT CCAAAAGTAAGCACTAAGTCTCATTTTATGAGACCACCATTTCTTAATATCACATCCAGTGCACCTTTG TCTTTCTGCCATATCTGAAATAAAACTATCAGTAATTCACATAGATAAACATAAGACTAAAGAAGTATA TTTACATTATCTGGAGAGTTTTGTTGCAGCTACGAGTTTGTATGGCAAATTCAATAATAAAGTATTGTT TATGCAAATTGC 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_001166060.2
Synonyms	HKPX2
Summary	This gene encodes the beta subunit of the glycine receptor, which is a pentamer composed of alpha and beta subunits. The receptor functions as a neurotransmitter-gated ion channel, which produces hyperpolarization via increased chloride conductance due to the binding of glycine to the receptor. Mutations in this gene cause startle disease, also known as hereditary hyperekplexia or congenital stiff-person syndrome, a disease characterized by muscular rigidity. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2009]
Locus ID	2743
MW	54.7

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