Synapsin I (SYN1) (NM_006950) Human Untagged Clone

CAT#: SC314473

SYN1 (untagged)-Human synapsin I (SYN1), transcript variant Ia



  "NM_006950" in other vectors (6)

CNY 5,168.00


货期*
现货

规格
    • 10 ug

Product images

经常一起买 (4)
Rabbit Polyclonal Anti-SYN1 Antibody
    • 100 ul

CNY 1,999.00
CNY 3,280.00


TurboFectin Transfection Reagent (1 mL in 1 vial)
    • 1 ml in 1 vial

CNY 4,090.00


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

CNY 1,280.00


Forward sequencing primer VP1.5, Reverse sequencing primer XL39, 100pmoles each
    • 100 pmol

CNY 480.00

Specifications

Product Data
Type Human Untagged Clone
Tag Tag Free
Synonyms EPILX; MRX50; SYN1a; SYN1b; SYNI
Vector pCMV6-XL6
E. coli Selection Ampicillin (100 ug/mL)
Mammalian Cell Selection None
Sequence Data
>OriGene sequence for NM_006950 edited
GGAGGTCTATATAAGCAGAGCTCATTTAGGTGACACTATAGAATACAAGCTACTTGTTCT
TTTTGCAGCGGCCGCGAATTCGGCACGAGGGCGGAGGAGTCGTGTCGTGCCTGAGAGCGC
AGCTGTGCTCCTGGGCACCGCGCAGTCCGCCCCCGCGGCTCCTGGCCAGACCACCCCTAG
GACCCCCTGCCCCAAGTCGCAGCCATGAACTACCTGCGGCGCCGCCTGTCGGACAGCAAC
TTTATGGCCAATCTGCCAAATGGGTACATGACAGACCTGCAGCGTCCGCAGCCGCCCCCA
CCGCCGCCCGGTGCCCACAGCCCCGGAGCCACGCCCGGTCCCGGGACCGCCACTGCCGAG
AGGTCCTCCGGGGTCGCCCCAGCGGCCTCTCCGGCCGCCCCTAGCCCCGGGTCCTCGGGG
GGCGGTGGCTTCTTCTCGTCGCTGTCCAACGCGGTCAAGCAGACCACGGCGGCGGCAGCT
GCCACCTTCAGCGAGCAGGTGGGCGGCGGCTCTGGGGGCGCAGGCCGCGGGGGAGCCGCC
TCCAGGGTGCTGCTGGTCATCGACGAGCCGCACACCGACTGGGCAAAATACTTCAAAGGG
AAAAAGATCCATGGAGAAATTGACATTAAAGTAGAACAGGCCGAATTCTCTGATCTCAAC
CTTGTGGCCCATGCCAATGGTGGATTCTCTGTGGATATGGAAGTTCTTCGGAATGGGGTG
AAGGTCGTGCGGTCTCTGAAGCCGGATTTTGTGCTGATCCGCCAGCACGCCTTCAGCATG
GCACGCAACGGAGACTACCGCAGTTTGGTCATTGGGCTGCAGTATGCTGGAATCCCCAGT
GTTAACTCCTTGCATTCTGTCTACAACTTCTGTGACAAGCCCTGGGTGTTTGCCCAGATG
GTTCGACTGCATAAGAAACTGGGGACAGAAGAATTCCCTCTAATTGATCAGACCTTCTAC
CCCAATCACAAAGAAATGCTCAGCAGTACAACGTACCCCGTGGTTGTGAAGATGGGGCAC
GCACACTCTGGGATGGGCAAGGTCAAGGTTGACAACCAGCATGACTTCCAGGACATCGCA
AGTGTCGTGGCACTGACCAAGACGTATGCCACTGCCGAGCCCTTCATCGATGCCAAATAT
GACGTGCGTGTCCAGAAGATTGGGCAGAACTACAAGGCCTACATGAGGACGTCAGTGTCA
GGGAACTGGAAGACCAATACTGGCTCTGCGATGCTGGAGCAAATTGCCATGTCTGACAGA
TACAAGCTGTGGGTGGACACGTGCTCAGAGATTTTTGGGGGACTGGACATCTGCGCAGTG
GAAGCGCTACATGGCAAGGACGGAAGGGATCACATCATTGAGGTGGTGGGTTCCTCCATG
CCGCTCATTGGTGACCACCAGGATGAAGACAAACAGCTCATCGTAGAGCTCGTGGTCAAC
AAGATGGCTCAGGCCCTGCCCCGGCAGCGACAGCGGGATGCCTCCCCTGGCAGGGGCTCC
CATGGCCAGACTCCGTCCCCAGGGGCCCTGCCCTTGGGCCGCCAGACCTCCCAGCAGCCC
GCAGGGCCCCCGGCTCAGCAGCGACCCCCACCACAGGGCGGCCCTCCACAGCCGGGTCCA
GGCCCCCAGCGCCAGGGACCCCCATTGCAGCAGCGCCCGCCCCCGCAGGGCCAGCAGCAC
CTTTCAGGCCTTGGACCCCCAGCTGGCAGCCCCCTGCCCCAGCGCCTTCCAAGTCCCACC
TCAGCGCCCCAGCAGCCCGCGTCCCAGGCCGCGCCGCCGACCCAGGGTCAAGGCCGCCAA
TCCCGGCCAGTGGCGGGAGGCCCCGGGGCGCCTCCAGCAGCCCGCCCGCCCGCCTCTCCG
TCTCCCCAGCGCCAGGCGGGCCCCCCACAGGCTACCCGTCAGACATCCGTCTCTGGCCCG
GCTCCGCCAAAGGCCTCTGGGGCCCCACCGGGCGGGCAGCAGCGCCAGGGCCCGCCCCAG
AAACCCCCAGGCCCAGCCGGCCCCACACGCCAGGCCAGCCAGGCGGGTCCCGTGCCCCGC
ACTGGGCCACCCACCACGCAGCAGCCTCGGCCCAGCGGCCCGGGCCCCGCTGGACGTCCC
AAACCACAGCTGGCCCAGAAACCCAGCCAGGACGTGCCGCCACCCGCCACCGCCGCTGCA
GGGGGACCTCCGCACCCCCAGCTCAACAAATCCCAGTCTCTGACCAATGCCTTCAACCTT
CCAGAGCCAGCCCCGCCCAGGCCCAGCCTTAGCCAGGACGAGGTGAAAGCTGAGACCATC
CGCAGCCTGAGGAAGTCTTTCGCCAGCCTCTTCTCCGACTGATACCCCACTCTGAGAACC
CCAAAATCCCTGGGCAACCCTTCTCTGGGCCCTGAATCCATTTCTCACTTTTGGAGTCTC
CAAATCCCTTGAGAACCCATCTCCCGGTTCTCCAAGATTCCACCTCTCATTCCTCAAGAT
CCCCGAGTACCTTGAGAAACCTGACTCCTCCTGGCCCTAAATCCGGTTCTCACATGTGGA
ATCCCCAAGTCCTTTTAGAACCCCACTCGTGGTCACTTCAGGATCTACTTCTGTTTTAGA
ACCTCTACATTCCTGAAGACCTCCGCCCCTGGTTTCCCCAGAGGGCGTTTTCCTTCCTGG
AAGTGCCCAAATACCAGGCAACCCATTGCAGAATCCCTTCCTGGAGCCCTGAAGTTCCTG
GAAAACCCTATTTTTGGTCCCAAATCTCTCCAGCACACCTATTTCCCATCATAATTTTCC
AAATCCTCAAGAAACCCCTACTGTTGAGCCCCTTCCCATGGATCTTCCATCCCTCTGAAG
ATCCACATCTTCAAATGCCACCCAACACCTAGCCCCACAAGGATTTCCCTTCACCAGCTC
CCCTCAACCTCATTCAATACCTTGGGAGCCCCTCCCACTTCCAGGACCCCTCGGTTCCCC
CAGGGACCCCCTCCCCAGTTTCCTGCCTCTGACAGCTGTCTTTAAATATGCAAACTCCAC
CCATCTTCCCAGAATCCTTTGCACACGGAAGGCCAGTGGTCTCCGCTTCCCCACCTTTGC
TGTGGTGTCTGTGTCTGTGACTGACGTGGCCTCCTTTTGTGCCGTGCTTGGCATATGTGG
TCCTCGTTCATCGTGCCGCCTGTGGTGATGCGTGCAGTGACGCTGTTTATGTGGTCCGCA
CCTCCCCCTGACCTTCACTCCTTGCCTGGACTCACCCCACCCCTCAGCGGCTCTGAACCC
CAAGAGAAGAGTCGGGAAACAAAATAAACAAGCAAAGGCCCAGCAAAAAAAAAAAAAAAA
A
Restriction Sites Please inquire     
ACCN NM_006950
Insert Size 3300 bp
OTI Disclaimer Our molecular clone sequence data has been matched to the reference identifier above as a point of reference. Note that the complete sequence of our molecular clones may differ from the sequence published for this corresponding reference, e.g., by representing an alternative RNA splicing form or single nucleotide polymorphism (SNP).
OTI Annotation The full-length insert was fully sequenced and ORF exactly matches with that of NM_006950.2.
Product Components The ORF clone is ion-exchange column purified and shipped in a 2D barcoded Matrix tube containing 10ug of transfection-ready, dried plasmid DNA (reconstitute with 100 ul of water).
Reconstitution 1. Centrifuge at 5,000xg for 5min.
2. Carefully open the tube and add 100ul of sterile water to dissolve the DNA.
3. Close the tube and incubate for 10 minutes at room temperature.
4. Briefly vortex the tube and then do a quick spin (less than 5000xg) to concentrate the liquid at the bottom.
5. Store the suspended plasmid at -20°C. The DNA is stable for at least one year from date of shipping when stored at -20°C.
Reference Data
RefSeq NM_006950.2, NP_008881.2
RefSeq Size 2248 bp
RefSeq ORF 2118 bp
Locus ID 6853
UniProt ID P17600
Domains Synapsin
Gene Summary This gene is a member of the synapsin gene family. Synapsins encode neuronal phosphoproteins which associate with the cytoplasmic surface of synaptic vesicles. Family members are characterized by common protein domains, and they are implicated in synaptogenesis and the modulation of neurotransmitter release, suggesting a potential role in several neuropsychiatric diseases. This member of the synapsin family plays a role in regulation of axonogenesis and synaptogenesis. The protein encoded serves as a substrate for several different protein kinases and phosphorylation may function in the regulation of this protein in the nerve terminal. Mutations in this gene may be associated with X-linked disorders with primary neuronal degeneration such as Rett syndrome. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]
Transcript Variant: This variant (Ia) represents the longer transcript, and encodes the longer isoform (Ia). This isoform (Ia) contains a distinct domain E, as compared to isoform Ib.
*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.

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