Cathepsin K (CTSK) (NM_000396) Human 3' UTR Clone

Specifications

Product Data
Product Name	Cathepsin K (CTSK) (NM_000396) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	CTS02; CTSO; CTSO1; CTSO2; PKND; PYCD
ACCN	NM_000396
Insert Size	621 bp
Sequence Data	Insert Sequence (showhide) >SC207804 3’UTR clone of NM_000396 The sequence shown below is from the reference sequence of NM_000396. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC GCCAACCTGGCCAGCTTCCCCAAGATGTGACTCCAGCCAGCCAAATCCATCCTGCTCTTCCATTTCTTC CACGATGGTGCAGTGTAACGATGCACTTTGGAAGGGAGTTGGTGTGCTATTTTTGAAGCAGATGTGGTG ATACTGAGATTGTCTGTTCAGTTTCCCCATTTGTTTGTGCTTCAAATGATCCTTCCTACTTTGCTTCTC TCCACCCATGACCTTTTTCACTGTGGCCATCAGGACTTTCCCTGACAGCTGTGTACTCTTAGGCTAAGA GATGTGACTACAGCCTGCCCCTGACTGTGTTGTCCCAGGGCTGATGCTGTACAGGTACAGGCTGGAGAT TTTCACATAGGTTAGATTCTCATTCACGGGACTAGTTAGCTTTAAGCACCCTAGAGGACTAGGGTAATC TGACTTCTCACTTCCTAAGTTCCCTTCTATATCCTCAAGGTAGAAATGTCTATGTTTTCTACTCCAATT CATAAATCTATTCATAAGTCTTTGGTACAAGTTTACATGATAAAAAGAAATGTGATTTGTCTTCCCTTC TTTGCACTTTTGAAATAAAGTATTTATCTCCTGTCTACAGTTTAATAAATAGCATCTAGTACACATTCA 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_000396.4
Synonyms	CTS02; CTSO; CTSO1; CTSO2; PKND; PYCD
Summary	The protein encoded by this gene is a lysosomal cysteine proteinase involved in bone remodeling and resorption. This protein, which is a member of the peptidase C1 protein family, is predominantly expressed in osteoclasts. However, the encoded protein is also expressed in a significant fraction of human breast cancers, where it could contribute to tumor invasiveness. Mutations in this gene are the cause of pycnodysostosis, an autosomal recessive disease characterized by osteosclerosis and short stature. [provided by RefSeq, Apr 2013]
Locus ID	1513
MW	23.3

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