Peroxidase Labeling Kit-NH2

Peroxidase Labeling Kit-NH2

Catalog Number:
CFA1349672DOJ
Mfr. No.:
LK11-10
Price:
$445
  • Size:
    3 samples
    Quantity:
    Add to Cart:
      • Overview
        • Peroxidase Labeling Kit-NH2 is used mainly for the preparation of peroxidase-labeled IgG for enzyme immunoassay (EIA) and for the preparation of peroxidase-labeled antigen for competitive EIA. NH2-reactive peroxidase, a component of this kit, has succinimidyl groups (NHS) and reacts with proteins or other molecules that have an amino group in their structures. This kit contains all the reagents necessary for the labeling process, including storage buffer. The labeling process is simple: mix IgG with NH2-reactive peroxidase and incubate at 37°C for 2 hours. The NH2-reactive peroxidase forms a covalent link with the target molecule without any activation process. The distance of the NHS from peroxidase is about 1.2 nm, half of the radius of the peroxidase molecule. Therefore, when the peroxidase-labeled IgG is used for EIA, the labeling efficiency of the NH2-reactive peroxidase is high enough to eliminate the purification process after labeling. Also, peroxidase labeling will not affect the affinity of the target molecule. If a high-purity conjugate is required after labeling, simply use an affinity column or a gel-permeation column. When labeling small molecules, excess molecules can be removed by using the filtration tubes included in this kit. Because the amino groups of NH2-reactive peroxidase are blocked, no self-conjugation is possible.

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      • Properties
        • Categories
          Enzyme labeling
          Storage
          0-5°C
          Shipping
          with blue ice

          * For research use only

      • Applications
        • Application
          Western blot; Microscopy; Microplate assay
      • Reference
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          5) S. Takatsuka, T. Inukai, S. Kawakubo, T. Umeyama, M. Abe, K. Ueno, Y. Hoshino, Y. Kinjo, Y. Miyazaki, and S. Yamagoe, "Identification of a Novel Variant Form of Aspergillus fumigatus CalC and Generation of Anti-CalC Monoclonal Antibodies", Med Mycol J., 2019, 60, (1), 11.

          6) T. Sasaki, K. Liu,T. Agari, T. Yasuhara, J. Morimoto, M. Okazaki, H. Takeuchi, A. Toyoshima, S. Sasada, A. Shinko, A. Kondo, M. Kameda, I. Miyazaki, M. Asanuma, CV. Borlongan, M. Nishibori, and I. Date, "Anti-high mobility group box 1 antibody exerts neuroprotection in a rat model of Parkinson's disease", Exp. Neurol.., 2016, 275, 220.

          7) T. Tsumuraya, I. Fujii, M. Inoue, A. Tatami, K. Miyazaki, and M. Hirama, "Production of monoclonal antibodies for sandwich immunoassay detection of ciguatoxin 51-hydroxyCTX3C", Toxicon., 2006, 48, (3), 287.

          8) W. Jin, K. Yamada, M. Ikami, N. Kaji, M. Tokeshi, Y. Atsumi, M. Mizutani, A. Murai, A. Okamoto, T. Namikaw, Y. Baba, and M. Ohta, "Application of IgY to sandwich enzyme-linked immunosorbent assays, lateral flow devices, and immunopillar chips for detecting staphylococcal enterotoxins in milk and dairy products", J. Microbiol. Methods., 2013, 92, (3), 323.

          9) W.W.P.N. Weerakoon, M. Sakase, N. Kawate, M.A. Hannan, N. Kohama, and H. Tamada, "Plasma IGF-I, INSL3, testosterone, inhibin concentrations and scrotal circumferences surrounding puberty in Japanese Black beef bulls with normal and abnormal semen", Theriogenology., 2018, 114, (1), 54.

          10) Y. Watanabe, Y. Kazuki, K. Kazuki, M. Ebiki, M. Nakanishi, K. Nakamura, M. Yoshida Yamakawa,H. Hosokawa, T. Ohbayashi, M. Oshimura, and K. Nakashima, "Use of a Human Artificial Chromosome for Delivering Trophic Factors in a Rodent Model of Amyotrophic Lateral Sclerosis", Mol Ther Nucleic Acids., 2015, 4, (10), e253.

          11) Y.S. Kim, D.H. Jung, I.S. Lee, B.J. Pyun and J.S. Kim, "Osteomeles schwerinae extracts inhibits the binding to receptors of advanced glycation end products and TGF-β1 expression in mesangial cells under diabetic conditions", Phytomedicine., 2016, 23, (4), 388.

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