SHANK3 (NM_001080420) Human 3' UTR Clone

CAT#: SC216941

3' UTR clone of SH3 and multiple ankyrin repeat domains 3 (SHANK3) for miRNA target validation



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CNY 5795.00


货期*
3周

规格
    • 10 ug

Product images

推荐一起购买 (2)
Firefly luciferase assay kit, 150 assays
    • 1 kit

CNY 1520.00


DH5α Chemically Competent Cells (≥10^8 cfu/μg of pUC19 DNA)
    • 5 x 200 ul

CNY 1280.00

Specifications

Product Data
Product Name SHANK3 (NM_001080420) Human 3' UTR Clone
Vector pMirTarget
Synonyms DEL22q13.3; KIAA1650; PROSAP2; PSAP2; SPANK-2
ACCN NM_001080420
Insert Size 1931 bp
Sequence Data
>SC216941 3’UTR clone of NM_001080420
The sequence shown below is from the reference sequence of NM_001080420. The complete sequence of this clone may contain minor differences, such as SNPs.
Blue=Stop Codon Red=Cloning site

GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG
TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC
CGCGCGCTCAGGCAGCTGGACGGCAGCTGACGCCCCACCCCCACTCCCGCCCCGGCCGTGCCCTGCCGG
CAGGGCCCCCCACCCCCACCCCGGGCCGCGGGCTCGGCCTGCCCCTTACGACGGCGCCCGGGCCAGGAA
TGTTGCATGAATCGTCCTGTTTGCTGTTGCTCGGAGACTCGCCCTGTACATTGCTTAGTGCCCTCACCG
GCCGCCCAGCCCACCCAGCGCACAGTCAGGAAGGGCGTGGACCAGGGAGGCTGGGGCGGGAGGTGCCGG
GGGTGGGGTGCCCTAGCGTGACCACCTCCTTCGCAGCTCCTGGTGGCCATTCTCCCAGAGGGGGAACCT
AGTCCAGCATGCGAGGTCAGGACCCGCCTTGGTGACTCGGGGGGAGGGGGGAGACATTGGGATTCTCGA
TGGGGGCCAAGGAGCCCCCCTGTTTTGCATATTTTAATCCACTCTATATTTGGAACGAGAAAAGGAACA
AATATCTCTGTCCGTAATAGTTTCCTCTCCCCTCCCTTCTACTTCCACTGGTCCCACTGCAGCTGCCCA
GTCTTCCATCTCCGGCCCCTCACTGCCACTGCCACCCCACAACGGGGCAGGGGACGCTCCAGCTGGTCT
GGGGTTGGCCAGGGCCCTAGTGGCCCGCCCTGGGGCCCCAGCTCGGCCCCTCGCCTCGCTGAGCTCTAG
TGTGCCCCACCGACCCTTCAGGTGCTGCTCGTGGTGGGAGGGGCGGCAGGCCGCGGGTCCTGCTGTGCA
CCCGCGGGACCAGCCGGCCTGGGAGACCATCGGCCGGGGGGGATGAGGGCAGGGCCCTGCCGCTCCACC
GCAGCCATCTTCCTCACAGGGTCTCTCCCCAAGGAGGGGGCTAGCTTGGTCCCCATGCTCTTGGGCAAC
TACAGCAGAGAAGCCTCCCTGCCTTGGACCCCAAAGTCTCCTGTCCTGCCCTTTATGTGTGTGGGTGAA
ACTGGGTGCGTCTGAGCACGTGGGAGCCGTGTGTGTGCCTGATTACTGAGTGGCCACCAGGGGCCGCTC
TGGACTAGCGCGGGGCCGTGGAGGCGTGCACCGTGTGCATGCGTGGGGTGTACCTGTGAGAGCACCCTG
TCTCCTCTTCCAAAGAAAGTCAGAGGCCATCCTGCACCCTGGGTCCAGCTGTTTGCCCAGCCTGTCCTT
CCAGAGCCTCACCCAGCCTGAGCGGGGTTCCCTGGTGAATCCCTGCTGCTTGGGGAGGCCCCAAGGGCC
CCTTGGAGGCAGCGCCCCCACCTTGGGCTTCTGAGGGCATCATAGGGGGACCCCTAGAGTCAGTTCACC
ACAGGCCCTGGGGAGAGTCAAAGACCCCCGAGGGTGCCCAGCCCCCCACACTGTGACTCCTCACACTCA
GCGATGACCTGTGGGGTGGGGGGCCCTGGGACGTTTTTAAACCTAGGGTTTGGAGTCTGGACTAAGCTC
CATCCACGTCACTCACAAGTTTCTGTTTATATTTCTAGCTTTTTTTAATAAAATAAAAAAAAAAAGAAA
ACAGAAGTTTTCACAACCCAGGGGCCTGGCACGCCGGTCTGTGCCTGCCCGCCCCGCCCTGGCCCACCG
GCCCCACTCCCTGGGCACAGAGTCACACCCACTCATCCTTCCGCCAACAGTCCAGGTCACACAGCAGCA
GTCACTGTAACAGACTGCCACATACACACTCGGTCTCACACTCACCTGTGGGTTTTGGTTCCGTTCAAT
TTGGGTTTTTAACTTTACAGGGTCAGTTCCGCTTCACCTCCTTTTGTATGGAGTTCCATCCGGGGGGTT
TCACCCCCTGCTCCAGTCCTGAGGCCTCCTGACCCTGACGTTGTGATACGCCCCACAGAGATCTATGTT
TCTTATATTATTATTATTGATAATAATTATTATAATATTATTATGTAATAAATTTATAAGAAATGAAG
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_001080420.1
Synonyms DEL22q13.3; KIAA1650; PROSAP2; PSAP2; SPANK-2
Summary This gene is a member of the Shank gene family. Shank proteins are multidomain scaffold proteins of the postsynaptic density that connect neurotransmitter receptors, ion channels, and other membrane proteins to the actin cytoskeleton and G-protein-coupled signaling pathways. Shank proteins also play a role in synapse formation and dendritic spine maturation. Mutations in this gene are a cause of autism spectrum disorder (ASD), which is characterized by impairments in social interaction and communication, and restricted behavioral patterns and interests. Mutations in this gene also cause schizophrenia type 15, and are a major causative factor in the neurological symptoms of 22q13.3 deletion syndrome, which is also known as Phelan-McDermid syndrome. Additional isoforms have been described for this gene but they have not yet been experimentally verified. [provided by RefSeq, Mar 2012]
Locus ID 85358
MW 68.4
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