ATP13A2 (NM_001141973) Human 3' UTR Clone

Specifications

Product Data
Product Name	ATP13A2 (NM_001141973) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	CLN12; HSA9947; KRPPD; PARK9; SPG78
ACCN	NM_001141973
Insert Size	293 bp
Sequence Data	Insert Sequence (showhide) >SC203305 3’UTR clone of NM_001141973 The sequence shown below is from the reference sequence of NM_001141973. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC CCGCCGCTGCCCGCCGGCCCCCTGAGGTAGTGCAGGCCCACGGGCACCCCAGACACTGGAACTCCCTGC CTCTGAGCCACCAACTGGACCCCTCTCCAGCAACACCACCGCCACCACCTCCCACATCCCTGAGGTTGG CGACTGTCTACACTCCTCCCCCGAGACCACCCCCACCCTGGGGAAGCGTTGACTACTGTCCCCTACCTT GGACCATCCCGCGTAGGGGTGGCAGCCCCCAGCTCCCCTCAGTGCTGCTGTCAGTGTAGCAAATAAAGT CATGATATTTTCCTGGC 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_001141973.3
Synonyms	CLN12; HSA9947; KRPPD; PARK9; SPG78
Summary	This gene encodes a member of the P5 subfamily of ATPases which transports inorganic cations as well as other substrates. Mutations in this gene are associated with Kufor-Rakeb syndrome (KRS), also referred to as Parkinson disease 9. Multiple transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Nov 2008]
Locus ID	23400
MW	10.6

*Delivery time may vary from web posted schedule. Occasional delays may occur due to unforeseen complexities in the preparation of your product. International customers may expect an additional 1-2 weeks in shipping.