GBE1 (NM_000158) Human 3' UTR Clone

Specifications

Product Data
Product Name	GBE1 (NM_000158) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	APBD; GBE; GSD4
ACCN	NM_000158
Insert Size	734 bp
Sequence Data	Insert Sequence (showhide) >SC209310 3’UTR clone of NM_000158 The sequence shown below is from the reference sequence of NM_000158. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC ATCCTTCAGAATGTGGATCTGCCGAATTGAAGAGGCCTGATTTCAGCTCCACCAGATGCAGATTTGTGT TTTGTTTTCTTGTTATCACTGTCACACAGCTTATAACATGTATGCTTTTCAGAATACAGTTGTCTAGCC AAGCCATCAAGTGTCTGAAATTCAATATTGGTTTATGCAAATACAGCAAACTTTTATTTAAGTAGATGG GAGAATATGTTTAAAATATTAGGAATCCTAGACCATATTTTCAAGTCATCTTAGCAGCTAGGATTCTCA AATGGAAGTGTTATATATAATATGTTAAAAACATTTTGCTTTCCTGGCTAATTATTTGATCCTTTTAAA TTCAAATTTGAATCATTTGTCATGTATGATTATTTCTGTTAAATGTACACAGTATTTAAGATGGATATT TGGTGGCTCTATTTGTTCTGATATCTTTTGGTCTAAATTATGAGGTACCAAGATTGTTTCTTTGTTTCT TTTTTTCAAATTGTGTTTAGAAATACTGTAATAAATATGCAGTAGTGATATAAAGAATTATATCCAAGG TAATATAAAAGCCATTACGTATGAACTCATCCGTGTCTCATTTTGTGTTTTATTTTGTGATCTCTTGTC CACTAAGTATCTTGTTAAATGCCAGTATCTCAGTCTTTCTGAAGCCCTGAAATGGTAATTGTAGCATTT CAGAAAATGTCTTTCATTTCAATCAATAAAAAGCTTTTGTAAAA 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_000158.4
Synonyms	APBD; GBE; GSD4
Summary	The protein encoded by this gene is a glycogen branching enzyme that catalyzes the transfer of alpha-1,4-linked glucosyl units from the outer end of a glycogen chain to an alpha-1,6 position on the same or a neighboring glycogen chain. Branching of the chains is essential to increase the solubility of the glycogen molecule and, consequently, in reducing the osmotic pressure within cells. Highest level of this enzyme are found in liver and muscle. Mutations in this gene are associated with glycogen storage disease IV (also known as Andersen's disease). [provided by RefSeq, Jul 2008]
Locus ID	2632
MW	28.6

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