CATSPER2 (NM_172097) Human 3' UTR Clone

Specifications

Product Data
Product Name	CATSPER2 (NM_172097) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	MGC33346
ACCN	NM_172097
Insert Size	893 bp
Sequence Data	Insert Sequence (showhide) >SC210567 3’UTR clone of NM_172097 The sequence shown below is from the reference sequence of NM_172097. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC GAGATCCTGAGGGTTCGTTTAGTGGGATGAAGAATGTGCCTAGGTGAATCGAAAGAACAAGTTAACATG ATAATAGGAAGAAACAAAAATTTACTTAACTTCTTTCTTTTGATTTTTTTTCCCTAAAACTAAACATCA ATCATTGCAGGAGTTGTTGGTATTAGGAGCAAAGTAGACTAACTACAACATCAATGCCAACAAGAGCAT CTGCCGGTTACTGAGCACTTACTAAGTGCCAAGCATTATTTTAAGTGTTTTCCTTACATTATCTCATTT ATGCTCCACAACAACCCAATTAAATAACCATGAATTTTATCCCCCTTTTTATATCTGAACAAGTTTAAG TATAGTGTTTAAGCAACTTAATATAGAAAGGCTGAATAGTAAGCACTTCTCAGAGAATGCTATTCAAGG GATAACGCCCAGGGAACAATGAAGAGGATAAGATGAAGAAGCTGCAATTCTGCCTGGGTGCCTTGGGGT GTATTTTACTTATAACCTGTGTGTTTTCCACAGTCCCTGCTTCCCGAGGTTGTGGTATTGGTAGGGGTA ACAGGCCAATCGGTGTGGCTTCAGCTTCTGAGGATCTGCCGGGTGCTGAGGTCTCTCAAACTCCTTGCA CAATTCCGTCAAATTCAAATTATTATTTTGGTCCTGGTCAGGGCCCTCAAGGTGATTTGACTGTTGCAA GCTAAAGCAGGGGGCAAGGTAGATAAATGTGAGGGCTTAACATAGAATATGAAACAAATTGGCCGGGTG CGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAAGCCGAGGGGGATGGGTCATGAGGTCAGGAGTTC GAGACCAGCCTGACCAACATGGTGAAACCCTGTCTCTACTAAAAATACCAAAAAAAAAAAAAAAA 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_172097.1
Synonyms	MGC33346
Summary	This gene encodes a member of a family of cation channel proteins that localize to the flagellum of spermatozoa. Defects at this locus causes male infertility. Alternatively spliced transcript variants have been observed at this locus. Readthrough transcription originates upstream of this locus in diphosphoinositol pentakisphosphate kinase 1 pseudogene 1 and is represented by GeneID:110006325. Related pseudogenes are found next to this locus on chromosome 15 and on chromosome 5. [provided by RefSeq, Mar 2017]
Locus ID	117155
MW	34.2

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