KLC2 (NM_001134776) Human 3' UTR Clone
CAT#: SC211543
3' UTR clone of kinesin light chain 2 (KLC2) transcript variant 4 for miRNA target validation
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CNY 4,845.00
货期*
3周
规格
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经常一起买 (2)
Specifications
Product Data | |
Product Name | KLC2 (NM_001134776) Human 3' UTR Clone |
Vector | pMirTarget |
ACCN | NM_001134776 |
Insert Size | 934 bp |
Sequence Data |
>SC211543 3’UTR clone of NM_001134776
The sequence shown below is from the reference sequence of NM_001134776. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC CTCTCCCGACGAAGCTCCCTGGTGGGCTAATGCTGAAGGGGCAGCCAGTCACCAGAGCGCCCACCTGGC ACACCCCCCTCACCCCAGCCCTGCGCATGGGCCTGCTGCTTGTCCCGCCTGTCTCTCCCACAGCCCCTG TCTTTTCTGTTCAATCTCAGGGTAACCTTCTCCCTTGTCATCTCAGCCTGAGCCCTGGAGGCTGGGCCT GCCCACTCCAGCTCCATCCCTTATTTATTCCTTCCAGCAGGGCCCTCTTCCCTAGGTTCGGGCCAGCAG GAGGTGCCGGCTGGAGTCTCCACCATAGACTCAGTGGCCTGGCCTCCCCAGACCCCAGAGCCAAGAACA CTAAGCACTCGCCGGCCCTTCGGCACCCTCGCCCTCCCTCCCGACTCAACCCGGCCGTTGCTTCTGTAT ATAGAGAAATAAGTTATTGGCCGCGCGCCTCCCTTCAGTCCACGGTACTACCCGGGCCTCCCCTCGTCC CTCTTCTAGTGGTACCGCCCAGGCCTTAATCACCCCCATTCCGTGCGGTGGTATCTCCCAGGCTCTACA TTCTCGGGAGCGGCGCCTCCCAAGGGGGTCCTGGGACCTTCTCGCGCTCCTCCTGGCCTCTGAGGGATG CGTCCTACCCGCGCCATCGCCCCGTGGCCCAGGACGGGGACCTCCCCTTAGTCCGTCCTCCCACCGCCG GGCCCTGCCCCGCATCCCGGCCTTATGCACTGCCCCTCCCACCCGGCCCCGCCCAGGCACGGCCGACCC CGCCCCGGGCACCGCCCACCGAGCCATCCTGCCTCGCCTCCCCCCACGCCTGCAGCTTCTCGCGAGGGG CGGCGACGGTCCCCTGGTGGCAGGAGGGGCTCCCCCTGTTGCGGGTGAGGCGGCTGCTCTCATATTTTC AGATGTTGCTGTAGAAATAAAGACGGTTTAAATCTGA 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_001134776.2 |
Summary | The protein encoded by this gene is a light chain of kinesin, a molecular motor responsible for moving vesicles and organelles along microtubules. Defects in this gene are a cause of spastic paraplegia, optic atrophy, and neuropathy (SPOAN) syndrome. [provided by RefSeq, Mar 2016] |
Locus ID | 64837 |
MW | 33.1 |
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