产品名称
抗-磷酸-TrkB(Tyr816)抗体, from rabbit, purified by affinity chromatography
biological source
rabbit
antibody form
affinity isolated antibody
antibody product type
primary antibodies
clone
polyclonal
purified by
affinity chromatography
species reactivity
mouse, rat
species reactivity (predicted by homology)
gorilla (based on 100% sequence homology), bovine (based on 100% sequence homology), porcine (based on 100% sequence homology), human (based on 100% sequence homology), horse (based on 100% sequence homology)
technique(s)
immunocytochemistry: suitable
immunohistochemistry: suitable
immunoprecipitation (IP): suitable
western blot: suitable
NCBI accession no.
UniProt accession no.
shipped in
wet ice
target post-translational modification
phosphorylation (pTyr816 )
Quality Level
Gene Information
human ... NTRK2(4915)
rat ... Ntrk2(25054)
Analysis Note
蛋白质印迹分析:该抗体的1:500稀释液在10 µg BDNF处理的鼠TrkB转染的HEK293细胞裂解物中检测到磷酸化TrkB(Tyr816)。
Application
免疫沉淀分析:代表性批次免疫沉淀来自表达转染TrkB的BDNF刺激的HEK293细胞的Tyr816磷酸化TrkB(由Dr. Moses V. Chao, Langone Medical Center, New York University提供)。
蛋白质印迹分析:代表性批次在产后P9–P10大鼠的皮质切片以及腹膜内注射Dex注射的P18-20大鼠的背侧纹状体中检测到地塞米松-(Dex-)和BDNF诱导的TrkB Tyr816磷酸化(Jeanneteau, F., et al. (2008).Proc Natl Acad Sci USA.105(12):4862-4867)。
蛋白质印迹分析:代表性批次在小鼠脑突触制备物中检测到TrkB Tyr816磷酸化(C.N., et al. (2013).Cell.155(7):1596-1609)。
蛋白质印迹分析:代表性批次在培养的小鼠海马神经元和表达鼠TrkB的HEK293细胞中检测到BDNF刺激的TrkB Tyr816磷酸化(Bath, K.G., et al. (2008).J. Neurosci. 28(10):2383-2393)。
免疫组织化学分析:代表性批次在接受甲吡酮和/或地塞米松治疗后的产后P18大鼠的齿状回组织切片中检测到增强的TrkB Tyr816磷酸化(Jeanneteau, F., et al. (2008).Proc Natl Acad Sci USA.105(12):4862-4867)。
免疫组化分析:代表性批次在来自成年小鼠的嘴侧迁移流(RMS)的冠状切片中检测到TrkB Tyr816磷酸化(ath, K.G., et al. (2008).J. Neurosci. 28(10):2383-2393)。
免疫细胞化学分析:代表性批次在5小时饥饿的大鼠海马神经元培养中检测到皮质酮刺激的TrkB Tyr816磷酸化(Jeanneteau, F., et al. (2008).Proc Natl Acad Sci USA.105(12):4862-4867)。
免疫细胞化学分析:代表性批次在来自E16.5大鼠胚胎的培养DRG神经元中检测到BDNF刺激的TrkB Tyr816磷酸化(Arevalo, J.C., et al. (2006).Neuron.50(4):549-559)。
发育信号转导
神经科学
Biochem/physiol Actions
Disclaimer
General description
Immunogen
Other Notes
Physical form
Preparation Note
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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
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A major focus of breast cancer research is to understand the mechanisms responsible for disease progression and drug resistance. Toward that end, it has been found that approximately two thirds of all human breast carcinomas overexpress the Estrogen Receptor α (ERα) protein and it remains the primary pharmacological target for endocrine therapy1,2. The normal cellular function of ERα is as a transcription factor that mediates a wide variety of physiological processes, many of which are dependent upon phosphorylation of the receptor at specific amino acid residues3,4. Indeed, ERα is known to be phosphorylated at a multitude of different sites, yet how these all correlate to disease remains unclear5. Here, we interrogated multiple sites of ERα for phosphorylation status by screening an extensive panel of different breast cancer patient samples and other non-breast cancer tissue microarray (TMA) slide samples to determine their relevance to disease.
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