推薦產品
生物源
guinea pig
品質等級
抗體表格
serum
抗體產品種類
primary antibodies
無性繁殖
polyclonal
物種活性
rhesus macaque, rat
物種活性(以同源性預測)
canine (based on 100% sequence homology), bovine (based on 100% sequence homology), human (based on 100% sequence homology), horse (based on 100% sequence homology), rhesus monkey (based on 100% sequence homology), chimpanzee (based on 100% sequence homology), mouse (based on 100% sequence homology)
技術
immunohistochemistry: suitable
western blot: suitable
NCBI登錄號
UniProt登錄號
運輸包裝
wet ice
目標翻譯後修改
unmodified
基因資訊
human ... GABBR2(9568)
一般說明
γ-氨基丁酸(GABA)是哺乳动物中枢神经紧张的系统中主要的抑制性神经递质。GABA通过离子型[GABA(A/C)]受体发挥其作用,以产生快速的突触抑制,而代谢型[GABA(B)]受体则产生缓慢,延长的抑制信号。GABA(B)受体由两个相关的7跨膜受体GABA(B)受体1和GABA(B)受体2的异二聚体组成。GABA(B)受体1基因被定位到靠近HLA-F基因的HLA I类区域内的染色体6p21.3。多发性硬化、癫痫和精神分裂症的易感基因座也已定位于该区域。该基因的可变剪接产生4个转录物变体。
特異性
该抗体可识别大鼠GABA-B-R2的C端。
免疫原
在大鼠GABA-B-R2的C末端的牛甲状腺球蛋白偶联的线性肽。
應用
抗GABAB受体R2抗体是用于IH & WB的抗GABAB受体R2的抗体。
品質
通过免疫组化对大鼠中脑区浦肯野细胞进行了评估。
免疫组化分析: 该抗体的1:300稀释液在大鼠中脑区域的浦肯野细胞中检测到GABA-B-R2。
免疫组化分析: 该抗体的1:300稀释液在大鼠中脑区域的浦肯野细胞中检测到GABA-B-R2。
標靶描述
尽管在计算的105 kDa分子量周围观察到一条条带,但由于该条带与存在的其他非特异性条带相比较弱,因此该抗体不推荐使用蛋白质印迹法。
聯結
替代品:AB5394
分析報告
对照
大鼠中脑区的浦肯野细胞
大鼠中脑区的浦肯野细胞
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儲存類別代碼
12 - Non Combustible Liquids
水污染物質分類(WGK)
WGK 1
閃點(°F)
Not applicable
閃點(°C)
Not applicable
分析證明 (COA)
輸入產品批次/批號來搜索 分析證明 (COA)。在產品’s標籤上找到批次和批號,寫有 ‘Lot’或‘Batch’.。
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Multiplexed optical imaging provides holistic visualization on a vast number of molecular targets, which has become increasingly essential for understanding complex biological processes and interactions. Vibrational microscopy has great potential owing to the sharp linewidth of vibrational spectra. In 2017
The European journal of neuroscience, 32(8), 1265-1277 (2010-09-18)
The stimulation of inhibitory neurotransmitter receptors, such as γ-aminobutyric acid type B (GABA(B) ) receptors, activates G protein-gated inwardly-rectifying K(+) (GIRK) channels, which influence membrane excitability. There is now evidence suggesting that G protein-coupled receptors and G protein-gated inwardly-rectifying K(+)
Molecular medicine reports, 15(2), 975-980 (2016-12-31)
Chemotherapeutic drugs commonly induce peripheral neuropathic pain, which limit their clinic use. In the present study, the effect of fucoidan on the development of vincristine‑induced neuropathic pain was evaluated and the underlying mechanism was examined. A neuropathy model was established
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