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Western Blot analysis of IgG and IgM antibodies against?R. helvetica?whole cell antigen demonstrates the lipopolysaccaride (LPS) ladders and specific reactions against?R. helvetica?proteins in the 110?150-kDa region in serum for IgG for patients 1, 32 and 33 and for IgM for patients 3, 8, 10, 17, 20 and 22 in dilution 1:200. Lane P(h) demonstrates specific proteins and the LPS ladders reacting with a positive human serum and P(r) with a polyclonal rabbit antiserum. N(h) represent a negative human serum control. Secondary antibody Anti-human IgG DyLight?549 (p/n 609?142-123 ) and Anti-human IgM DyLight? 549 (p/n 609?142-007). Figure 1. PMID: 34712390.
Western Blot analysis of IgG antibodies against?R.?helvetica?whole cell antigen. Lane A-P demonstrates the lipopolysaccaride ladders and specific reactions against?R.?helvetica?proteins in the 110-150-kDa region for serum 2 for patients (Lane) V16(A), V43(B), V46 (C)(Area V); S71(D), S72(E), S75(F), V6(G) (Area O); K7(H), K9(I), K14(J), K46(K) K56(L) (Area K); A13(M), A16(N), A23(O), A35(P) (Area A) in titres 1:200. Lane P(h) demonstrates specific proteins and the lipopolysaccharide (LPS) ladders reacting with a human antiserum from a patient diagnosed with rickettsial infection and N(h) a healthy negative blood donor. Mw = molecular weight marker. “Fig 2” is compiled of four figure panels representing the groups of lanes that originated from different gels/blots (Gel A-D). The short vertical lines of “Fig 2” divide the individual non-adjacent lanes in the gels. The original analyses are presented in?S1?S4?Figs with Gels A-D as Supporting Information. Fig 2. PMID: 27846275.
702 Peptides are printed in duplicates randomly distributed on the microarray. Control peptides (HA and FLAG controls) are located in a square surrounding the peptides of interest. As secondary antibody DyLight? 549 conjugated goat anti-human IgG antibody and for the FLAG control peptide a mouse anti-FLAG-Cy3 antibody were used; microarrays were read using a Fujifilm Life Science FLA-5100 imaging system with a SHG 532nm (green) diode laser and an LPG filter. Fig e1. PMID: 26894206.
Properties of DyLight? Conjugates.
DyLight? dyes can be used for two-color western blot detection with low background and high signal. Anti-tubulin was detected using a DyLight? 549 conjugate. Anti-TNFa was detected using a DyLight? 649 conjugate. The image was captured using the Typhoon? 9410 Imaging System.
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Western Blot analysis of IgG and IgM antibodies against?R. helvetica?whole cell antigen demonstrates the lipopolysaccaride (LPS) ladders and specific reactions against?R. helvetica?proteins in the 110?150-kDa region in serum for IgG for patients 1, 32 and 33 and for IgM for patients 3, 8, 10, 17, 20 and 22 in dilution 1:200. Lane P(h) demonstrates specific proteins and the LPS ladders reacting with a positive human serum and P(r) with a polyclonal rabbit antiserum. N(h) represent a negative human serum control. Secondary antibody Anti-human IgG DyLight?549 (p/n 609?142-123 ) and Anti-human IgM DyLight? 549 (p/n 609?142-007). Figure 1. PMID: 34712390.
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| 別品名 |
Goat Anti Human IgG DyLight 549TM Conjugated Antibody, Goat Anti-Human IgG Antibody DyLight 549TM conjugation
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| 交差種 |
Human
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| 非交差(吸収処理)種 |
Mouse Rat Bovine Rabbit Chicken Sheep Goat Guinea Pig Hamster Equine
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| 適用 |
Enzyme Linked Immunosorbent Assay Dot Blot
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| 免疫動物 |
Goat
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| 標識物 |
DyLightTM 549
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| 精製度 |
Affinity Purified
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| 参考文献 |
[Pub Med ID]27846275
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| [注意事項] |
濃度はロットによって異なる可能性があります。メーカーDS及びCoAからご確認ください。
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| メーカー |
品番 |
包装 |
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RKL
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609-142-123
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100 UG
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※表示価格について
| 当社在庫 |
なし
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| 納期目安 |
約10日
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| 法規制 |
毒
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| 保存温度 |
4℃
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