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主营:化学试剂,CCK-8试剂盒,细胞检测,自噬研究,化学标记,生化试剂等
℡ 4000-520-616
℡ 4000-520-616
Dojindo/Fluorescein Labeling Kit-NH2/3/LK01
产品编号:LK01
市  场 价:¥0.00
场      地:美国(厂家直采)
产品分类: 蛋白类>多肽>多肽合成>
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Dojindo/Fluorescein Labeling Kit-NH2/3/LK01
商品介绍
DescriptionReferencesQ & AManualS.D.S

Product DescriptionFluorescein Labeling Kit-NH2 is mainly used for the preparation of fluorescein-labeled proteins such as IgG for immunostaining and cellular proteins for tracing. Amine-reactive fluorescein, a component of this kit, has succinimidyl groups (NHS) that react with the amino groups on proteins or other molecules (Fig. 1). This kit contains all the reagents necessary for labeling, including storage buffer. Each vial of fluorescein can label up to 200 μg of IgG, conjugating about 4 to 6 fluorescein molecules per IgG molecule. Because this kit also includes a buffer exchange system, a sample containing amine base buffer can be labeled. Although membrane filtration sometimes causes IgG aggregation, the buffer system in this kit prevents aggregation during the concentration of IgG or fluorescein-labeled IgG solution. A fluorescein-labeled IgG solution prepared using this kit is stable for more than 2 months at 4ºC. The excitation and emission wavelengths of the fluoresceinlabeled IgG are 495 nm and 520 nm, respectively (Fig. 2).

Fig. 1 IgG labeling reaction of NH2-reactive fluorescein

Fig. 2 Fluorescence spectrum of fluorescein-conjugated IgG______excitation spectrum______emission spectrum

Precaution♦ The molecular weight of the protein to be labeled with this kit should be greater than 50,000.♦ IgG or fluorescein-conjugated IgG is always on the membrane of the filtration tube during the labeling process.♦ If the IgG solution contains other proteins with molecular weight greater than 10,000, such as BSA or gelatin, purify the IgG solution before labeling fluorescein with this kit. IgG solution can be purified by IgG Purification Kits (not included in this kit).♦ If the IgG solution contains small insoluble material, centrifuge the solution and use the supernatant for the labeling.

1. M. Hiyoshi, S. Suzu, Y. Yoshidomi, R. Hassan, H. Harada, N. Sakashita, H. Akari, K. Motoyoshi and S. Okada, “Interaction between Hck and HIV-1 Nef Negatively Regulates Cell Surface Expression of M-CSF Receptor”, Blood, 2008, 111(1), 243.2. W. Aung, A. Tsuji, H. Sudo, A. Sugyo, T. Furukawa, Y. Ukai, Y. Kurosawa and T. Saga, “Immunotargeting of Integrin α6β4 for Single-Photon Emission Computed Tomography and Near-Infrared Fluorescence Imaging in a Pancreatic Cancer Model”, Molecular Imaging, 2016, 15, 1.3. S. Abe, K. Yamamoto, M. Kurata, S. Abe-Suzuki, R. Horii, F. Akiyama and M. Kitagawa, “Targeting MCM2 function as a novel strategy for the treatment of highly malignant breast tumors”, Oncotarget., 2015, 6, (33), 34892.4. K.M. Nishida, T.N. Okada, T. Kawamura, T. Mituyama, Y. Kawamura, S. Inagaki, H. Huang, D. Chen, T. Kodama, H. Siomi and M.C. Siomi, “Functional involvement of Tudor and dPRMT5 in the piRNA processing pathway in Drosophila germlines”, EMBO J.., 2009, 28, (24), 3820.5. P.G. Sreekumar, R. Kannan, M. Kitamura, C. Spee, E. Barron, S.J. Ryan and D.R. Hinton, “αB crystallin is apically secreted within exosomes by polarized human retinal pigment epithelium and provides neuroprotection to adjacent cells”, PLoS ONE., 2010, 5, (10), e12578.6. R. Asano, T. Kumagai, K. Nagai, S. Taki, I. Shimomura, K. Arai, H. Ogata, M. Okada, F. Hayasaka, H. Sanada, T. Nakanishi, T. Karvonen, H. Hayashi, Y. Katayose, M. Unno, T. Kudo, M. Umetsu and I. Kumagai, “Domain order of a bispecific diabody dramatically enhances its antitumor activity beyond structural format conversion: the case of the hEx3 diabody”, Protein Eng. Des. Sel.., 2013, 26, (5), 359.7. R. Asano, I. Shimomura, S. Konno, A. Ito, Y. Masakari, R. Orimo, S. Taki, K. Arai, H. Ogata, M. Okada, S. Furumoto, M. Onitsuka, T. Omasa, H. Hayashi, Y. Katayose, M. Unno, T. Kudo, M. Umetsu and I. Kumagai, “Rearranging the domain order of a diabody-based IgG-like bispecific antibody enhances its antitumor activity and improves its degradation resistance and pharmacokinetics”, MAbs., 2014, 6, (5), 1243.8. R. Asano, K. Ikoma, I. Shimomura, S. Taki, T. Nakanishi, M. Umetsu and I. Kumagai, “Cytotoxic enhancement of a bispecific diabody by format conversion to tandem single-chain variable fragment (taFv): the case of the hEx3 diabody”, J. Biol. Chem.., 2011, 286, (3), 1812.9. T. Toyotome, M. Yamaguchi, A. Iwasaki, A. Watanabe, H. Taguchi, L. Qin, H. Watanabe and K. Kamei, “Fetuin A, a serum component, promotes growth and biofilm formation by Aspergillus fumigatus”, Int. J. Med. Microbiol.., 2012, 302, (2), 108.10. W. Ma, V. Schubert, M. M. Martis, G. Hause, Z. Liu, Y. Shen, U. Conrad, W. Shi, U. Scholz, S. Taudien, Z. Cheng and A. Houben, “The distribution of α-kleisin during meiosis in the holocentromeric plant Luzula elegans”, Chromosome Res.., 2016, 24, (3), 393.11. Y. Yokoi, K. Nakamura, T. Yoneda, M. Kikuchi, R. Sugimoto, Y. Shimizu and T. Ayabe, “Paneth cell granule dynamics on secretory responses to bacterial stimuli in enteroids”, Sci. Rep.., 2019, 9, 2710.12. Y.J. Lee, S.R. Han, N.Y. Kim, S.H. Lee, J.S. Jeong and S.W. Lee, “An RNA aptamer that binds carcinoembryonic antigen inhibits hepatic metastasis of colon cancer cells in mice”, Gastroenterology., 2012, 143, (1), 155.

Can I use this kit for other proteins?

Yes, if the molecular weight is greater than 50,000.

Do I have to use a Filtration tube prior to labeling the protein?

If the protein solution does not contain small molecules with an amino group and the concentration of the protein is 10 mg per ml, or about 70 μM, there is no need to use the Filtration tube. Just mix 10 μl of the sample solution with 90 μl of Reaction buffer and add 8 μl NH2-reactive fluorescein (prepared at step 3) to the mixture, and follow the protocol starting at step 4.

How long is the fluorescein-labeled protein stable?

If you store at 4ºC, it is stable for over 2 months. For longer storage, add 100% volume of glycerol, aliquot, and store at -20ºC. However, please note that stability depends on the protein itself.

What is the minimum amount of IgG that can be labeled by this kit?

The minumum amount of IgG is 10 μg; simply follow the protocol. The labeling ratio remains the same for 10 μg to 100 μg of IgG.

Can I use this kit to label oligonucleotides or peptides?

No. Oligonucleotides and peptides may be too small to retain on the membrane filter of the Filtration tube.

Related Categories Labeling Chemistry

品牌介绍

Dojindo Molecular Technologies,Inc.是美国领先的生命科学研究专用试剂盒和化学品分销商。我们通过提供优质的支持和创新产品,不断扩大客户的满意度,以扩大生命科学研究和开发领域。

我们的公司文化反映出“ Jin”(仁)字符背后的含义,即尊重和关爱他人。当我们公司执行上述任务时,“ Jin”精神始终处于我们思想的最前沿。  


我们如何开始

1996年

作为日本Dojindo实验室的子公司,Dojindo Molecular Technologies,Inc.在马里兰州盖瑟斯堡开业,这是新产品开发的主要设施。开发了诸如DNA损伤定量试剂盒SOD检测试剂盒WST标记试剂盒系列之类的产品,为全球客户提供现成的检测试剂盒。


2000

Dojindo Molecular Technologies,Inc.成为了另一个销售地点,将Dojindo产品带到了北美地区的研究专业人员手中。


2008年

我们搬迁至马里兰州罗克维尔,仅专注于北美的销售和营销活动。我们目前的位置非常接近美国国立卫生研究院(NIH),美国国家癌症研究所(NCI),FDA,约翰·霍普金斯大学的研究人员。


我们不仅向周边地区,而且向我们在美国,加拿大和南美的客户提供日本优质的客户支持和创新产品。

关于同人堂实验室

Dojindo Laboratories由螯合化学领域的著名研究人员上野敬平教授创立。同人堂实验室是1951年第一家将EDTA(乙二胺四乙酸)商业化的日本公司。自那以后,同人堂实验室一直在生产用于支持科学研究进展的试剂。Dojindo实验室的任务是开发用于生命科学研究的创新工具。Dojindo实验室致力于通过科学发现和开发新药物为改善生活质量做出贡献。


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