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1 IgY's immunoreactivity and specificity were examined via
2 IgY/IgYDeltaFc antibodies purified from the eggs of DNA-
3 ovel care pathway that utilizes anti-Fel d 1 IgY antibodies to safely and effectively neutralize Fel
4 g product ingredient containing anti-Fel d 1 IgY antibodies was demonstrated in vitro, ex vivo, and i
6 results of the application of anti-Cor a 14 IgY electrochemical immunosensor to incurred foods estab
8 first time the scalability of anti-COVID-19 IgY production for effective distribution and potential
13 ely low affinity complex, but a 2:1 CHIR-AB1/IgY interaction allows an increase in apparent affinity
14 Peptides that were highly enriched against IgY from at least 4 out of 10 infected chickens were sel
15 ified as being enriched specifically against IgY from multiple animals infected with S. Enteritidis c
16 FcRY forms a compact structure containing an IgY binding site at acidic pH but undergoes a conformati
20 oglobulin is detected by treatment with anti-IgY labeled with horse radish peroxidase (Anti-IgY-HRP).
26 y peptides that were preferentially bound by IgY from chickens infected with Salmonella Typhimurium o
30 assays using specific rabbit IgG and chicken IgY were developed, and the assays had sensitivities of
31 1 was shown to bind the Fc region of chicken IgY and to induce calcium mobilization via association w
33 n neutralizing TGF-beta1 antibody or control IgY, the frequency of endocapillary apoptotic cells was
34 tration of 12,000 NAU/kg of duck egg-derived IgY/IgYDeltaFc protected hamsters when administered up t
36 es of monomeric and dimeric FcRY and an FcRY-IgY complex and explored FcRY's pH-dependent binding mec
41 sted in ELISA were highly discriminatory for IgY following S. Enteritidis infection (p < 0.05) compar
43 ns and to measure antibody specifically from IgY fractions of monospecific chicken antibody preparati
44 a precision medicine approach, we generated IgY antibodies against cytolysin from hyperimmunized chi
46 atidis contained significant amounts of IgM, IgY, and IgX antibodies that bind to B. dendrobatidis.
47 Neutralizing anti-TGF-beta1 or non-immune IgY were infused into the renal arteries of 3-d-old rats
51 turtles (Chelonia mydas) have a 5.7S 120-kDa IgY comprising two equally sized H/L chains with truncat
52 /L chains with truncated Fc and a 7S 200-kDa IgY comprised of two differently sized H chains bound to
61 e chicken egg yolk immunoglobulin Y (IgY) or IgY antibody to S. mutans GBP-B was supplied in lower (e
64 d stability testing showed that the purified IgY and tablets maintained activity and stability for ov
69 by immunoprecipitation with pU(L)17-specific IgY at 16 h postinfection, followed by mass spectrometry
70 nked immunosorbent assay to measure specific IgY production following immunization with keyhole limpe
71 immunofluorescence studies demonstrated that IgY binding and endocytosis occurred at acidic but not b
79 stocompatibility complex homolog), transfers IgY across the avian yolk sac, and represents a new clas
81 effect of specific chicken immunoglobulin Y (IgY) antibodies against cytolysin in vitro and in a micr
82 strate that the polyclonal immunoglobulin Y (IgY) antibodies prepared against affinity-purified Acant
83 Preimmune chicken egg yolk immunoglobulin Y (IgY) or IgY antibody to S. mutans GBP-B was supplied in
86 est antibody (anti-chicken immunoglobulin Y [IgY] or anti-human IgG), and the bound complex is measur
87 ody generated in chickens (immunoglobulin Y [IgY]) against the whole toxin suppressed cytokine respon