生物源
rabbit
品質等級
抗體表格
affinity isolated antibody
抗體產品種類
primary antibodies
無性繁殖
polyclonal
純化經由
affinity chromatography
物種活性
human
物種活性(以同源性預測)
feline (based on 100% sequence homology), porcine (based on 100% sequence homology), mouse (based on 100% sequence homology), bovine (based on 100% sequence homology)
技術
western blot: suitable
NCBI登錄號
UniProt登錄號
運輸包裝
dry ice
目標翻譯後修改
phosphorylation (pSer682 )
基因資訊
human ... SIRT1(23411)
1 of 4
本產品 | SAB5700048 | SAB5700606 | PLA0132 |
|---|---|---|---|
| Quality Level 100 | Quality Level 100 | Quality Level 100 | Quality Level 100 |
| antibody form affinity isolated antibody | antibody form affinity isolated antibody | antibody form affinity isolated antibody | antibody form affinity purified immunoglobulin |
| biological source rabbit | biological source rabbit | biological source rabbit | biological source rabbit |
| Gene Information human ... SIRT1(23411) | Gene Information human ... SIRT1(23411) | Gene Information human ... SIRT1(23411) | Gene Information rabbit ... Sirt1(23411) |
| technique(s) western blot: suitable | technique(s) immunofluorescence: 1:50-1:200, immunohistochemistry: 1:50-1:200, immunoprecipitation (IP): 1:50-1:100, western blot: 1:500-1:2000 | technique(s) immunofluorescence: 1:50-1:200, western blot: 1:500-1:2000 | technique(s) immunoprecipitation (IP): 1-4 μg/mg, western blot: 1:2,000- 1:10,000 |
| clone polyclonal | clone polyclonal | clone polyclonal | clone - |
一般說明
免疫原
應用
生化/生理作用
分析報告
Western Blotting Analysis: 1.0 µg/mL of this antibody detected phospho SIRT1 (Ser682) in 10 µg of Nocodazole treated cell lysate.
其他說明
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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’.。
相關內容
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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