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化工儀器網>產品展廳>試劑標物>生化試劑>其它生化試劑>IPKine™ Anti-HA Magnetic IP Kit IPKine™ HA標簽蛋白免疫沉淀試劑盒(磁珠法)

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IPKine™ Anti-HA Magnetic IP Kit IPKine™ HA標簽蛋白免疫沉淀試劑盒(磁珠法)

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亞科因生物技術有限公司

成立于2017年,總部位于中國武漢。公司專注于細胞分析檢測領域,經過多年的積累,目前生產和銷售的產品能夠全面、系統地覆蓋細胞代謝、細胞凋亡、細胞增殖、細胞氧化應激、細胞損傷與修復、細胞活力、遷移、侵襲、趨化、干細胞等相關生物學研究領域,為生命科學研發人員提供豐富、高質量的研究工具。



細胞代謝、細胞凋亡、細胞增殖、細胞氧化應激、細胞損傷與修復、細胞活力、遷移、侵襲、趨化、干細胞

商品信息

產品英文名稱 IPKine™ Anti-HA Magnetic IP Kit
產品中文名稱 IPKine™ HA標簽蛋白免疫沉淀試劑盒(磁珠法)

商品屬性

免疫原合成多肽
試劑盒組分
Non-Denaturing Lysis Buffer
TBS (10×)
Anti-HA Magnetic Beads
Mouse IgG Magnetic Beads
Elution Buffer
Neutralization Buffer
HA Peptide (25×)
SDS-PAGE Loading Buffer (5×)
特點&優勢? 高效:特異性強、靶蛋白結合量高,≥0.6 mg HA標簽融合蛋白/mL磁珠;
? 便捷:可結合多種形式的HA標簽蛋白(N端HA融合蛋白、C端HA融合蛋白);
? 通用:提供IP實驗所需的所有必要緩沖液;
? 可靠:提供陰性對照,可排除IgG本身和目的蛋白或其它特定生物分子的非特異性結合;
? 靈活:本試劑盒提供三種洗脫方法(HA多肽競爭洗脫、酸洗脫和SDS-PAGE Loading Buffer洗脫方法)。
保存建議按各組分標簽提示分開存儲,保質期12個月。
運輸條件冰袋運輸(藍冰)
警告本文列出的產品僅供研究使用,不適用于人類或臨床診斷。我們產品所推薦應用,不是建議使用我們的產品去違反任何或許可證。對于使用本產品可能發生的侵權或其他違規行為,我們不承擔任何責任。

附加信息

背景Human influenza hemagglutinin (HA) is a surface glycoprotein required for the infectivity of the human virus. The HA tag is derived from the HA-molecule corresponding to amino acids 98-106 has been extensively used as a general epitope tag in expression vectors. Many recombinant proteins have been engineered to express the HA tag, which does not appear to interfere with the bioactivity or the biodistribution of the recombinant protein.

圖片及說明

Figure. The immunoprecipitation effect of Anti-HA Magnetic IP Kit used for HA-Tag fusion protein. HEK293T cells were transfected with HA-Tag plasmid. Lane 1 was whole cell lysate (WCL); Lane 2 was the immunoprecipitation sample of Mouse IgG Magnetic Beads eluted by 1×SDS-PAGE Loading Buffer; Lane 3 was the immunoprecipitation sample of Anti-HA Magnetic Beads eluted by 1×SDS-PAGE Loading Buffer. Lane 4 was the immunoprecipitation sample of Anti-HA Magnetic Beads eluted by Elution Buffer; Lane 5 was the immunoprecipitation sample of Anti-HA Magnetic Beads eluted by Working HA Peptide. By using peptide elution and acid elution, only contained HA-Tag fusion protein, did not contain heavy and light chains of antibody.

Figure. The immunoprecipitation effect of Anti-HA Magnetic IP Kit used for HA-Tag fusion protein. HEK293T cells were transfected with HA-Tag plasmid. Lane 1 was whole cell lysate (WCL); Lane 2 was the immunoprecipitation sample of Mouse IgG Magnetic Beads eluted by 1×SDS-PAGE Loading Buffer; Lane 3 was the immunoprecipitation sample of Anti-HA Magnetic Beads eluted by 1×SDS-PAGE Loading Buffer. Lane 4 was the immunoprecipitation sample of Anti-HA Magnetic Beads eluted by Elution Buffer; Lane 5 was the immunoprecipitation sample of Anti-HA Magnetic Beads eluted by Working HA Peptide. By using peptide elution and acid elution, only contained HA-Tag fusion protein, did not contain heavy and light chains of antibody.



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