生物源
rabbit
品質等級
共軛
unconjugated
抗體表格
serum
抗體產品種類
primary antibodies
無性繁殖
polyclonal
物種活性
mouse, rat, human
技術
neutralization: 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 ... PNLIP(5406)
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本產品 | SAB1406269 | AV33851 | HPA062494 |
|---|---|---|---|
| antibody form serum | antibody form purified immunoglobulin | antibody form IgG fraction of antiserum | antibody form affinity isolated antibody |
| Quality Level 100 | Quality Level 100 | Quality Level 100 | Quality Level 100 |
| biological source rabbit | biological source mouse | biological source rabbit | biological source rabbit |
| shipped in wet ice | shipped in dry ice | shipped in wet ice | shipped in wet ice |
| Gene Information human ... PNLIP(5406) | Gene Information human ... PNLIP(5406) | Gene Information human ... PNLIP(5406) | Gene Information human ... PNLIP(5406) |
| UniProt accession no. | UniProt accession no. | UniProt accession no. | UniProt accession no. |
一般說明
免疫原
應用
Signaling
Signaling Neuroscience
Western Blotting Analysis: A representative lot detected both wild-type and W340X mutated recombinant human pancreatic lipase-related protein-2 (PLRP2) in culture media and lysates from transfected 293T and COS-7 cells (Xiao, X., et al. (2011) J. Biol. Chem. 286(30):26353-26363).
Neutralizing Analysis: A representative lot inhibited colipase-dependent pancreatic lipase-related protein-2 (PLRP2) enzymatic activity in pancreas extracts from 4-day old mice (D′Agostino D, and Lowe ME. (2004) J. Nutr. 134(1):132-134).
生化/生理作用
外觀
準備報告
Handling Recommendations: Upon receipt and prior to removing the cap, centrifuge the vial and gently mix the solution. Aliquot into microcentrifuge tubes and store at -20°C. Avoid repeated freeze/thaw cycles, which may damage IgG and affect product performance.
分析報告
Western Blotting Analysis: A 1:5,000 dilution of this antibody detected Pancreatic Lipase/PNLIP in 10 µg of human pancreas tissue lysate.
其他說明
免責聲明
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儲存類別代碼
10 - Combustible liquids
水污染物質分類(WGK)
WGK 1
分析證明 (COA)
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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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