T5942
Monoclonal Anti-14-3-3 θ/τ antibody produced in mouse
clone 3B9, purified immunoglobulin, buffered aqueous glycerol solution
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UNSPSC Code:
12352203
MDL number:
Conjugate:
unconjugated
Clone:
3B9, monoclonal
Application:
ARR, IP, WB
Citations:
2
biological source
mouse
conjugate
unconjugated
antibody form
purified immunoglobulin
antibody product type
primary antibodies
clone
3B9, monoclonal
form
buffered aqueous glycerol solution
mol wt
antigen 31 kDa
species reactivity
rat, bovine, human, mouse
technique(s)
immunoprecipitation (IP): suitable, microarray: suitable, western blot: 1:5,000 using whole extracts of mouse 3T3, rat PC12, human Jurkat, or normal fibroblasts or bovine MDBK cells
isotype
IgG1
shipped in
wet ice
storage temp.
−20°C
target post-translational modification
unmodified
Gene Information
human ... YWHAQP4(646954)
mouse ... EG546165(546165)
Immunogen
Full-length, recombinant 14-3-3-2 θ/τ
Physical form
Solution in phosphate buffered saline, pH 7.5, containing 50% glycerol and 3 mM sodium azide.
Disclaimer
Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.
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Tsutomu Nakamura et al.
EBioMedicine, 34, 189-200 (2018-07-27)
GABAergic dysfunction underlies many neurodevelopmental and psychiatric disorders. GABAergic synapses exhibit several forms of plasticity at both pre- and postsynaptic levels. NMDA receptor (NMDAR)-dependent inhibitory long-term potentiation (iLTP) at GABAergic postsynapses requires an increase in surface GABAARs through promoted exocytosis;
Vijay Agarwal et al.
International journal of oncology, 42(3), 1088-1092 (2013-01-23)
We have previously shown that specific COX-2 inhibitors, including DuP 697, have anti-proliferative effects on mesothelioma cells and potentiate the cytotoxicity of pemetrexed. Here, we used a novel proteomic approach to explore the mechanism of action of this agent. COX-2-positive
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