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Merck
CN

04-855

抗-GluR1抗体,克隆C3T,兔单克隆

culture supernatant, clone C3T, Upstate®

别名:

Anti-GluA1, Anti-GluR-1, Anti-GluR-A, Anti-GluR-K1, Anti-GluR1

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关于此项目

UNSPSC Code:
12352203
NACRES:
NA.41
eCl@ss:
32160702
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产品名称

抗-GluR1抗体,克隆C3T,兔单克隆, culture supernatant, clone C3T, Upstate®

biological source

rabbit

conjugate

unconjugated

antibody form

culture supernatant

antibody product type

primary antibodies

clone

C3T, monoclonal

species reactivity

human, chimpanzee, rat, mouse

manufacturer/tradename

Upstate®

technique(s)

immunohistochemistry: suitable
immunoprecipitation (IP): suitable
western blot: suitable

isotype

IgG

NCBI accession no.

UniProt accession no.

shipped in

dry ice

target post-translational modification

unmodified

Quality Level

Gene Information

human ... GRIA1(2890)

Analysis Note

对照
已通过免疫印迹对大鼠脑微粒体制剂(12-144)进行常规评估
已通过蛋白免疫印迹对大鼠脑微粒体制剂进行了常规评估。

蛋白质印迹分析(WB):该批次的1:5,000 -1:10,000稀释液已在大鼠脑微粒体制剂(目录号12-144)中检测到GluR1。

Application

免疫沉淀在大鼠脑微粒体制剂中,2 μL先前批次的产品已对GluR1进行了免疫沉淀。

免疫组织化学:该抗体的先前批次已显示可检测人,小鼠和大鼠组织中的GluR1。
抗GluR1抗体,克隆C3T,可检测GluR1的水平 & 已出版&并经过验证可用于IH、IP&WB。
研究子类别
神经递质 & 受体
研究类别
神经科学

Biochem/physiol Actions

可识别GluR1,Mr 106 kDa。
根据100%序列同源性预测会与黑猩猩发生交叉反应。

Disclaimer

除非我们的产品目录或产品附带的其他公司文档另有说明,否则我们的产品仅供研究使用,不得用于任何其他目的,包括但不限于未经授权的商业用途、体外诊断用途、离体或体内治疗用途或任何类型的消费或应用于人类或动物。

General description

106 kDa
L谷氨酸是中枢神经系统中主要的兴奋性神经递质。谷氨酸能神经传递涉及正常脑功能的大多数方面,并且在许多神经病理学条件下都可能受到干扰。代谢型谷氨酸受体是G蛋白偶联受体家族,已分为3组。第一组包括GRM1,这些受体已显示可激活磷脂酶C。据报道,GRM1在大脑和脊髓的各个区域表达。EST已从大脑和眼睛库中分离出来。

Immunogen

对应于人GluR1氨基酸858-868(..TLPRNSGAGAS..)(成熟人GluR1氨基酸840-850)的KLH结合合成肽

Other Notes

替代:05-855

Physical form

0.05% 叠氮化钠中的培养上清液

Preparation Note

自运送之日起在-20°C可稳定保存2年。避免反复冻融。为了最大程度地回收产品,在融化后和取下盖子之前,将原始样品瓶进行离心。

Legal Information

UPSTATE is a registered trademark of Merck KGaA, Darmstadt, Germany

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存储类别

10 - Combustible liquids

wgk

WGK 2


分析证书(COA)

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Gonadectomy differentially regulates steroid receptor coactivator-1 and synaptic proteins in the hippocampus of adult female and male C57BL/6 mice.
Chen Bian,Kongjiang Zhu,Li Yang,Sen Lin,Shurong Li,Bingyin Su,Jiqiang Zhang
Synapse null
Membrane depolarization regulates AMPA receptor subunit expression in cerebellar granule cells in culture.
Incontro, S; Ramirez-Franco, J; Sanchez-Prieto, J; Torres, M
Biochimica et Biophysica Acta null
The striatal mosaic in primates: striosomes and matrix are differentially enriched in ionotropic glutamate receptor subunits.
Martin, L J, et al.
The Journal of Neuroscience, 13, 782-792 (1993)
Linli Qiu et al.
The Journal of steroid biochemistry and molecular biology, 156, 23-31 (2015-11-27)
Androgens have been proposed to play important roles in the regulation of hippocampus function either directly, through the androgen receptor (AR), or indirectly, through estrogen receptors (ERs), after aromatization into estradiol. Steroid receptor coactivator-1 (SRC-1) is present in the hippocampus
Zhexing Wen et al.
Nature, 515(7527), 414-418 (2014-08-19)
Dysregulated neurodevelopment with altered structural and functional connectivity is believed to underlie many neuropsychiatric disorders, and 'a disease of synapses' is the major hypothesis for the biological basis of schizophrenia. Although this hypothesis has gained indirect support from human post-mortem

相关内容

Glutamate is an excitatory neurotransmitter found in the synaptic vesicles of glutamatergic synapses. The post-synaptic neurons in these synapses contain ionotropic and metabotropic glutamate receptors. Glutamate binds to AMPA (α-amino-3-hydroxy-5- methylisoxazole-4-propionic acid) subtype glutamate receptors, leading to sodium influx into the post-synaptic cell and resulting in neuronal excitability and synaptic transmission. The NMDA (N-methyl-d-aspartate) subtype glutamate receptors, on the other hand, regulate synaptic plasticity, and can influence learning and memory. The metabotropic g-protein coupled mGluRs modulate downstream calcium signaling pathways and indirectly influence the synapse’s excitability. The synaptic architecture includes intracellular scaffolding proteins (PSD-95, GRIP), intercellular cell adhesion molecules (NCAMs, N-Cadherins), and a variety of signaling proteins (CaMKII/PKA, PP1/PP2B). Processes critical for synaptic transmission and plasticity are influenced by these molecules and their interactions. When the function of these molecules is disrupted, it leads to synaptic dysfunction and degeneration, and can contribute to dementia as seen in Alzheimer’s disease.

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