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Rabbit Anti-Gabrb3 (p-S408/S409) Polyclonal Antibody
Rabbit Anti-Gabrb3 (p-S408/S409) Polyclonal Antibody
GABA A Receptor beta 3; ECA5; GABA alpha receptor beta-2 subunit; GABA(A) receptor subunit beta-3; GABAA receptor beta 3 subunit; GABAA receptor subunit beta 3; GABR B3; Gabrb3; Gamma aminobutyric acid (GABA) A receptor beta 3; Gamma aminobutyric acid rec
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  • NO.:SLA0320
    concentration:1mg/ml
    React Species:Mouse, Rat
    Immunogen Species:Rabbit
    Clonality:Polyclonal
    Applications:WB
    Gene name:Gabrb3 (p-S408/S409)
    UniProt Entry:P63079
    NCBI Gene Entry:24922
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Product NameRabbit Anti-Gabrb3 (p-S408/S409) Polyclonal Antibody
Cat No.SLA0320
Chinese Name磷酸化G氨基丁酸受体3抗体
AliasGABA A Receptor beta 3; ECA5; GABA alpha receptor beta-2 subunit; GABA(A) receptor subunit beta-3; GABAA receptor beta 3 subunit; GABAA receptor subunit beta 3; GABR B3; Gabrb3; Gamma aminobutyric acid (GABA) A receptor beta 3; Gamma aminobutyric acid receptor subunit beta 3; Gamma-aminobutyric acid receptor subunit beta-3; GBRB3_HUMAN; MGC9051; RB3_RAT;Gabrb3 (S433/434);
Host SpeciesRabbit
IsotypeIgG
ClonalityPolyclonal
React SpeciesMouse,Rat
ApplicationsWB (1:500-2000)
Not yet tested in other applications.
Optimal working dilutions must be determined by the end user.
ImmunogenKLH conjugated Synthesised phosphopeptide derived from rat Gabrb3 around the phosphorylation site of Ser408/409
Purificationaffinity purified by Protein A
Concentration1mg/ml
Predicted MW.54 kDa
Subcellular LocationMembrane
Gene ID24922
Swiss-ProtP63079
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 encodes a member of the ligand-gated ionic channel family. The encoded protein is one the subunits of a multi-subunit chloride channel that serves as the receptor for gamma-aminobutyric acid, a major inhibitory neurotransmitter of the mammalian nervous system. This gene is located on the long arm of chromosome 15 in a cluster with two other genes encoding related subunits of the family. This gene may be associated with the pathogenesis of several disorders including Angelman syndrome, Prader-Willi syndrome, nonsyndromic orofacial clefts, epilepsy and autism. Alternatively spliced transcript variants encoding distinct isoforms have been described. [provided by RefSeq, Jul 2013]
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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