ライフサイエンスコーパス: IgY

1 IgY/IgYDeltaFc antibodies purified from the eggs of DNA-

2 arked flexibility of Fab arms of 7S and 5.7S IgY.

3 Measurement of the 1:1 CHIR-AB1/IgY interaction affinity indicates a relatively low affi

4 ely low affinity complex, but a 2:1 CHIR-AB1/IgY interaction allows an increase in apparent affinity

5 Peptides that were highly enriched against IgY from at least 4 out of 10 infected chickens were sel

6 ified as being enriched specifically against IgY from multiple animals infected with S. Enteritidis c

7 FcRY forms a compact structure containing an IgY binding site at acidic pH but undergoes a conformati

8 s induced elevated pathogen-specific IgM and IgY serum antibodies.

9 Y labeled with horse radish peroxidase (Anti-IgY-HRP).

10 The binding of the Anti-IgY-HRP is detected by recording the electrocatalytic si

11 oglobulin is detected by treatment with anti-IgY labeled with horse radish peroxidase (Anti-IgY-HRP).

12 termine model chicken antipeanut antibodies (IgY) in serum.

13 plasma was identified as IgG (also known as IgY), which has Galalpha1-4Gal in its heavy chains.

14 Avian IgY is closely related to an ancestor of both mammalian

15 a more elongated structure that cannot bind IgY.

16 Both IgY can be captured with protein G or melon gel, but les

17 y peptides that were preferentially bound by IgY from chickens infected with Salmonella Typhimurium o

18 Biotinylated rabbit polyclonal to chick IgY (rIgPxcIgY) and phosphorylthioate-modified oligoDNA

19 Chicken IgY was used for the detection and quantification of pea

20 goat IgG, mouse IgG, human IgG, and chicken IgY was demonstrated.

21 1 was shown to bind the Fc region of chicken IgY and to induce calcium mobilization via association w

22 n neutralizing TGF-beta1 antibody or control IgY, the frequency of endocapillary apoptotic cells was

23 tration of 12,000 NAU/kg of duck egg-derived IgY/IgYDeltaFc protected hamsters when administered up t

24 The natural "despeciation" of the duck IgY (i.e., Fc removed) results in an immunoglobulin pred

25 es of monomeric and dimeric FcRY and an FcRY-IgY complex and explored FcRY's pH-dependent binding mec

26 The cryoEM structure of the FcRY-IgY revealed symmetric binding of two FcRY heads to the

27 l transcytosis, and recycling of chicken FcY/IgY.

28 de (from 5 pg mL(-1) to 1 microg mL(-1)) for IgY antibody in undiluted calf serum.

29 sted in ELISA were highly discriminatory for IgY following S. Enteritidis infection (p < 0.05) compar

30 IgE-Fc and IgG-Fc, and the implications for IgY binding to its receptor are discussed.

31 ns and to measure antibody specifically from IgY fractions of monospecific chicken antibody preparati

32 termined to be less appropriate than an IgG (IgY)-based assay for use with free-ranging birds.

33 atidis contained significant amounts of IgM, IgY, and IgX antibodies that bind to B. dendrobatidis.

34 Neutralizing anti-TGF-beta1 or non-immune IgY were infused into the renal arteries of 3-d-old rats

35 here on the determination of immunoglobulin IgY.

36 vel as to how avian maternal immunoglobulin (IgY) is transferred to offspring.

37 f 72.4 degrees C and a sigmoidal decrease in IgY activity at TOD (ELISA) of 67.5 degrees C.

38 turtles (Chelonia mydas) have a 5.7S 120-kDa IgY comprising two equally sized H/L chains with truncat

39 /L chains with truncated Fc and a 7S 200-kDa IgY comprised of two differently sized H chains bound to

40 Maternal IgY, the avian counterpart of IgG, is transferred to emb

41 In birds, maternal IgY in egg yolk is transferred across the yolk sac to pa

42 During the first 3 days of IgY feeding, all animals were challenged with 5 x 10(6)

43 A recombinant fragment of IgY-Fc consisting of a dimer of the Cupsilon3 and Cupsil

44 entified in an ELISA using a training set of IgY samples.

45 e chicken egg yolk immunoglobulin Y (IgY) or IgY antibody to S. mutans GBP-B was supplied in lower (e

46 Polyclonal IgY antibodies specific for internal sialoside epitopes

47 In contrast, preimmune IgY did not influence either the adhesion of the parasit

48 used to immunize chickens and the resulting IgY fraction was purified from egg yolks.

49 We affinity-purified the chicken yolk sac IgY receptor (FcRY) and sequenced its gene.

50 The chicken yolk sac IgY receptor (FcRY) is the ortholog of the mammalian pho

51 by immunoprecipitation with pU(L)17-specific IgY at 16 h postinfection, followed by mass spectrometry

52 nked immunosorbent assay to measure specific IgY production following immunization with keyhole limpe

53 immunofluorescence studies demonstrated that IgY binding and endocytosis occurred at acidic but not b

54 alkali and reducing sugar) treatments on the IgY binding of peanut proteins was investigated.

55 All rhesus monkeys treated with the IgY specific for SEB up to 4 h after challenge survived

56 y ultrasonication in an aqueous buffer, then IgY is captured by incubation on the NEE.

57 with horseradish peroxidase (HRP) to bind to IgY on the sensor and provide amplified signals.

58 e that FcRY achieves pH-dependent binding to IgY through a conformational change.

59 Enteritidis compared to IgY from vaccinates, for both an attenuated and an inact

60 stocompatibility complex homolog), transfers IgY across the avian yolk sac, and represents a new clas

61 Thus, turtle IgY share some characteristics with mammalian IgG.

62 strate that the polyclonal immunoglobulin Y (IgY) antibodies prepared against affinity-purified Acant

63 Preimmune chicken egg yolk immunoglobulin Y (IgY) or IgY antibody to S. mutans GBP-B was supplied in

64 n antibodies but not avian immunoglobulin Y (IgY).

65 est antibody (anti-chicken immunoglobulin Y [IgY] or anti-human IgG), and the bound complex is measur

66 ody generated in chickens (immunoglobulin Y [IgY]) against the whole toxin suppressed cytokine respon