PPEF1 (NM_152226) Human 3' UTR Clone

Specifications

Product Data
Product Name	PPEF1 (NM_152226) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	PP7; PPEF; PPP7C; PPP7CA
ACCN	NM_152226
Insert Size	460 bp
Sequence Data	Insert Sequence (showhide) >SC205800 3’UTR clone of NM_152226 The sequence shown below is from the reference sequence of NM_152226. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC ATGAAACCTGATGTCACCAACCTTGGCTAAACACAAATGAGAGCTTCCCTCAGGCTCCCTGAAACAGCT AGGCCCAAATCACAAGTACAGTCCTTTCCAACACCCCTGAAATTCATAGTCAGTAGCAGAGAAAAGCAG ATCCCAATTCATCCCACAAACAGATGCATAGTATGGGTTTTGGAAGTCCCTAGCAAGCTGTTATTGGTA AGATTAGGTTAAATGTCAGTAATAGGATTTGGTTTCAGCATTAGTACCTACATATTGCCAGTGAGAAAC TGGGTTGGACCTAGTGGTGTTGTCGTGAGTGCCACCTAACCAGGAGGCCAGAGCGGTTTGAAAACATCC TGAAAGGAACTCATACAGCACAAGAGAAAACTACTAAGCTTGACATCTGTGAGTGACTGAGGGAGACAG GAGGAATACCAGGTTATTCATGGAATAAAGTCTTTCCATCTTTAAA 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_152226.2
Synonyms	PP7; PPEF; PPP7C; PPP7CA
Summary	This gene encodes a member of the serine/threonine protein phosphatase with EF-hand motif family. The protein contains a protein phosphatase catalytic domain, and at least two EF-hand calcium-binding motifs in its C terminus. Although its substrate(s) is unknown, the encoded protein has been suggested to play a role in specific sensory neuron function and/or development. This gene shares high sequence similarity with the Drosophila retinal degeneration C (rdgC) gene. Several alternatively spliced transcript variants, each encoding a distinct isoform, have been described. [provided by RefSeq, Jul 2008]
Locus ID	5475
MW	16.9

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