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关于此项目
UNSPSC Code:
12352203
NACRES:
NA.41
eCl@ss:
32160702
Conjugate:
unconjugated
Clone:
polyclonal
Application:
immunohistochemistry
western blot
western blot
Species reactivity:
rhesus macaque, rat
Citations:
6
Technique(s):
immunohistochemistry: suitable
western blot: suitable
western blot: suitable
Uniprot accession no.:
产品名称
抗-GABA B受体R2抗体, serum, from guinea pig
biological source
guinea pig
conjugate
unconjugated
antibody form
serum
antibody product type
primary antibodies
clone
polyclonal
species reactivity
rhesus macaque, rat
species reactivity (predicted by homology)
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)
technique(s)
immunohistochemistry: suitable
western blot: suitable
NCBI accession no.
UniProt accession no.
shipped in
wet ice
target post-translational modification
unmodified
Quality Level
Gene Information
human ... GABBR2(9568)
Other Notes
替代品:AB5394
Immunogen
在大鼠GABA-B-R2的C末端的牛甲状腺球蛋白偶联的线性肽。
Analysis Note
对照
大鼠中脑区的浦肯野细胞
大鼠中脑区的浦肯野细胞
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。
Application
抗GABAB受体R2抗体是用于IH & WB的抗GABAB受体R2的抗体。
Biochem/physiol Actions
该抗体可识别大鼠GABA-B-R2的C端。
General description
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。
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。
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存储类别
12 - Non Combustible Liquids
wgk
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
Liang Zhang et al.
Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 41(6), 1467-1476 (2015-10-27)
Cortical network hyper-excitability is a common phenotype in mouse models lacking the transcriptional regulator methyl-CPG-binding protein 2 (MeCP2). Here, we implicate enhanced GABAB receptor activity stemming from diminished cortical expression of the GABA transporter GAT-1 in the genesis of this
Yupeng Miao et al.
Nature communications, 12(1), 4518-4518 (2021-07-28)
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
Chuanyin Hu et al.
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
Khaled Zemoura et al.
The Journal of biological chemistry, 291(41), 21682-21693 (2016-08-31)
GABAB receptors are heterodimeric G protein-coupled receptors, which control neuronal excitability by mediating prolonged inhibition. The magnitude of GABAB receptor-mediated inhibition essentially depends on the amount of receptors in the plasma membrane. However, the factors regulating cell surface expression of
Khaled Zemoura et al.
Molecular neurobiology, 56(2), 1293-1309 (2018-06-09)
The G protein-coupled GABAB receptors, constituted from GABAB1 and GABAB2 subunits, are important regulators of neuronal excitability by mediating long-lasting inhibition. One factor that determines receptor availability and thereby the strength of inhibition is regulated protein degradation. GABAB receptors are
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