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Recombinant Rabbit Anti-SYN1 Monoclonal Antibody
Recombinant Rabbit Anti-SYN1 Monoclonal Antibody
EPILX; EPILX1; MRX50; SYN1a; SYN1b; SYNI; Syn-1; Syn1-S; SYN1_HUMAN; SYN1; Brain protein 4.1; Synapsin I; SYN1_MOUSE; SYN1_RAT; mental retardation, X-linked 50; Synapsin-1
Total $200.0
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  • NO.:SLA1042M
    concentration:1mg/ml
    React Species:Human, Mouse, Rat
    Immunogen Species:Rabbit
    Clonality:Recombinant
    Applications:WB, IHC-P, IHC-F, IF, ELISA, IP
    Gene name:SYN1
    UniProt Entry:P17600
    NCBI Gene Entry:6853
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Product NameRecombinant Rabbit Anti-SYN1 Monoclonal Antibody
Cat No.SLA1042M
Chinese Name神经突触素1重组兔单抗
AliasEPILX; EPILX1; MRX50; SYN1a; SYN1b; SYNI; Syn-1; Syn1-S; SYN1_HUMAN; SYN1; Brain protein 4.1; Synapsin I; SYN1_MOUSE; SYN1_RAT; mental retardation, X-linked 50; Synapsin-1
Host SpeciesRabbit
IsotypeIgG
ClonalityMonoclonal
Clone No.3F7
React SpeciesHuman,Mouse,Rat
ApplicationsWB (1:500-2000)
IHC-P (1:50-200)
IHC-F (1:50-200)
IF (1:50-200)
ELISA (1:5000-1000.)
IP (1:50-200)
Not yet tested in other applications.
Optimal working dilutions must be determined by the end user.
ImmunogenKLH conjugated synthetic peptide derived from human Synapsin I
Purificationaffinity purified by Protein A
Concentration1mg/ml
Predicted MW.85 kDa
Gene ID6853
Swiss-ProtP17600
Storage0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.
Shipped at 4℃. Store at -20℃ for one year. Avoid repeated freeze/thaw cycles.
BackgroundThis 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]
AttentionThis product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.

 

FOR RESEARCH USE ONLY. Not for use in diagnostic or therapeutic procedures.

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