CCKBR (NM_176875) Human 3' UTR Clone

Specifications

Product Data
Product Name	CCKBR (NM_176875) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	CCK-B; CCK2R; GASR
ACCN	NM_176875
Insert Size	614 bp
Sequence Data	Insert Sequence (showhide) >SC207749 3’UTR clone of NM_176875 The sequence shown below is from the reference sequence of NM_176875. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC ACCACCATCAGCACACTGGGCCCTGGCTGAGGAGTAGAGGGGCCGTGGGGGTTGAGGCAGGGCAAATGA CATGCACTGACCCTTCCAGACATACGAAACACAAACCACAACTGACACAGGAAACCAACACCCAAAGCA TGGACTAACCCCAACGCACAGGAAAAGGTAGCTTACCTGACACAAGAGGAATAAGAATGGAGCAGTACA TGGGAAAGGAGGCATGCCTCTGATATGGGACTGAGCCTGGCCCATAGAAACATGACACTGACCTTGGAG AGACACAGCGTCCCTAGCAGTGAACTATTTCTACACAGTGGGAACTCTGACAAGGGCTGACCTGCCTCT CACACACATAGATTAATGGCACTGATTGTTTTAGAGACTATGGAGCCTGGCACAGGACTGATTCTGGGA TGCTCCTAGTTTGACCTCACAGTGACCCTTCCCAATCAGCACTGAAAATACCATCAGGCCTAATCTCAT ACCTCTGACCAACAGGCTGTTCTGCACTGAAAAGGTTCTTCATCCCTTTCCAGTTAAGGACCGTGGCCC TGCCCTCTCCTTCCTTACCCAAACTGTTCAAGAAATAATAAATTGTTTGGCTTCCTCCTGAA 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_176875.4
Synonyms	CCK-B; CCK2R; GASR
Summary	This gene encodes a G-protein coupled receptor for gastrin and cholecystokinin (CCK), regulatory peptides of the brain and gastrointestinal tract. This protein is a type B gastrin receptor, which has a high affinity for both sulfated and nonsulfated CCK analogs and is found principally in the central nervous system and the gastrointestinal tract. Alternative splicing results in multiple transcript variants. A misspliced transcript variant including an intron has been observed in cells from colorectal and pancreatic tumors. [provided by RefSeq, Dec 2015]
Locus ID	887
MW	22.6

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