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The Fold ′n′ Glow Protein Solubility Assay kit allows a test protein to be expressed as an N-terminal fusion with a fluorescent protein [i.e., Green Fluorescent Protein (GFP), Cyan Fluorescent Protein (CFP), and Yellow Fluorescent Protein (YFP)]. This allows the detection of protein properly folded in a given sample as the folding reporter gives a signal directly proportional to the amount of correctly folded protein. The kit can be used for the detection and quantification of any protein by tagging and detecting either soluble or insoluble proteins.
特徴および利点
Fluorescent protein (GFP, CFP, or YFP) fusions and split protein tags are widely used for the analysis of protein. These large tags can perturb protein solubility, misfold, and alter the processing of the protein. The split fluorescent protein technology used in the "Fold ′n′ Glow" assay overcomes these problems. The protein tag is a genetically encoded, split fluorescent protein technology, engineered with small, soluble, self-associating fragments. Thus, it is a simple split fluorescent protein system that doesn′t change fusion protein solubility, or require chemical ligation, fused interacting partners, co-expression, or co-refolding. Furthermore, while fluorogenic biarsenical FlaSH or ReASH substrates also overcome these limitations, they also require many other conditions not necessarywhen using the split fluorescent protein technology. Thefluorescent protein system is a simple and easy tagging and detection system. These kits may be used to quantify the expression level of the tagged protein, to determine the solubility of a protein, or to determine the solubility of a protein′s domain.
適合性
This kit contains sufficient reagents for one 96 well plate (96 tests)
原理
The kit is a protein tagging and detection method that uses split fluorescent protein technology in a fluorescent complementation assay. The protein to be quantified is fused to a small fluorescent protein fragment (contained in the S11 plasmid) via a flexible linker. Expressed separately, neither the fusion protein of interest nor the fluorescent protein detector (Universal Detection Reagent S1-10) is fluorescent. When mixed, the properly folded fusion protein and detector spontaneously associate, completing the fluorophore. Misfolding or aggregation of the fusion protein makes the fluorescent protein tag inaccessible and prevents complementation, thus preventing fluorescence. Therefore, misfolded or aggregated proteins are not included in the quantification of the protein of interest.
法的情報
Fold 'n' Glow is a trademark of Sandia BioTech
保管分類コード
10 - Combustible liquids
引火点(°F)
Not applicable
引火点(℃)
Not applicable
適用法令
試験研究用途を考慮した関連法令を主に挙げております。化学物質以外については、一部の情報のみ提供しています。 製品を安全かつ合法的に使用することは、使用者の義務です。最新情報により修正される場合があります。WEBの反映には時間を要することがあるため、適宜SDSをご参照ください。
毒物及び劇物取締法
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PRTR
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消防法
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労働安全衛生法名称等を表示すべき危険物及び有害物
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労働安全衛生法名称等を通知すべき危険物及び有害物
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カルタヘナ法
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Jan Code
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試験成績書(COA)
製品のロット番号・バッチ番号を入力して、試験成績書(COA) を検索できます。ロット番号・バッチ番号は、製品ラベルに「Lot」または「Batch」に続いて記載されています。
New molecular reporters for rapid folding assays.
PLoS ONE, 3 (6) (2008)
Nature biotechnology, 17(7), 691-695 (1999-07-15)
Formation of the chromophore of green fluorescent protein (GFP) depends on the correct folding of the protein. We constructed a "folding reporter" vector, in which a test protein is expressed as an N-terminal fusion with GFP. Using a test panel
Nature biotechnology, 23(1), 102-107 (2004-12-08)
Existing protein tagging and detection methods are powerful but have drawbacks. Split protein tags can perturb protein solubility or may not work in living cells. Green fluorescent protein (GFP) fusions can misfold or exhibit altered processing. Fluorogenic biarsenical FLaSH or
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