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生物来源
mouse
质量水平
偶联物
Allophycocyanin conjugate
抗体形式
purified immunoglobulin
抗体产品类型
primary antibodies
克隆
S327-95, monoclonal
形式
buffered aqueous solution
分子量
antigen predicted mol wt 170 kDa
种属反应性
human, rat, mouse
浓度
1 mg/mL
技术
immunocytochemistry: suitable
immunohistochemistry: suitable
western blot: suitable
同位素/亚型
IgG2a
NCBI登记号
UniProt登记号
运输
wet ice
储存温度
−20°C
靶向翻译后修饰
unmodified
基因信息
rat ... Grin2a(24409)
一般描述
The GRIN2A (glutamate ionotropic receptor NMDA (N-methyl-D-aspartate) type subunit 2A) gene is mapped to human chromosome 16p13.2. It codes for a transmembrane ligand-gated ion channel called N-methyl-D-aspartate glutamate receptor α2 subunit.
免疫原
Fusion protein amino acids 75-325 (extracellular N-terminus) of rat GluN2A/NR2A
生化/生理作用
The GRIN2A (glutamate ionotropic receptor NMDA (N-methyl-D-aspartate) type subunit 2A) gene is associated with focal epilepsy and impaired speech. NMDA glutamate receptor α2 subunit is involved in neuron development, maintains synaptic plasticity and is associated with memory. GRIN2A is related to schizophrenia and Alzheimer′s disease. Mutations in GRIN2A gene upregulates NMDA action and might lead to melanoma tumors. NMDA participates in apoptosis and proliferation of cancer cells.
特点和优势
Evaluate our antibodies with complete peace of mind. If the antibody does not perform in your application, we will issue a full credit or replacement antibody. Learn more.
外形
PBS pH7.4, 50% glycerol, 0.09% sodium azide
免责声明
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.
WGK
WGK 1
闪点(°F)
Not applicable
闪点(°C)
Not applicable
法规信息
新产品
Epilepsy in patients with GRIN2A alterations: genetics, neurodevelopment, epileptic phenotype and response to anticonvulsive drugs
von Stupnagel C, et al.
European Journal of Paediatric Neurology, 21(3), 530-541 (2017)
GRIN2A mutations in epilepsy-aphasia spectrum disorders
Yang X, et al.
Brain & Development, 40(3), 205-210 (2018)
Selected GRIN2A mutations in melanoma cause oncogenic effects that can be modulated by extracellular glutamate
Dmello SAN, et al.
Cell Calcium, 60(6), 384-395 (2016)
Epilepsy-associated GRIN2A mutations reduce NMDA receptor trafficking and agonist potency-molecular profiling and functional rescue
Addis L, et al.
Scientific Reports, 7(1), 66-66 (2017)
2-methoxyestradiol impacts on amino acids-mediated metabolic reprogramming in osteosarcoma cells by its interaction with NMDA receptor
Gorska PM, et al.
Journal of Cellular Physiology, 232(11), 3030-3049 (2017)
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