Figure 6

Neutralizing scFv Antibodies against Infectious Bursal Disease Virus Isolated From a Nlpa-Based Bacterial Display Library

Tianhe Li*, Bing Zhou*, Tingqiao Yu, Ning Li, Xiaochen Guo, Tianyuan Zhang, Jingzhuang Zhao, Liming Xu, Siming Li, Lei Ma, Tingting Li, Liangjun Ding, Mingzhe Sun, Deshan Li and Jiechao Yin

Published: 21 February, 2017 | Volume 1 - Issue 1 | Pages: 001-011

aac-aid1001-g006

Figure 6:

ELISA analysis of the binding ability of anti-VP2 scFvs to VP2. The plates were coated with different concentrations (300 μg/mL,60 μg/mL,12 μg/mL,2.4 μg/mL) of scFvs, followed by incubation with VP2, chicken egg yolk antibody and secondary antibody. control1 (without VP2 or IBDV strains), control2 (without egg yolk antibody), control3 (without VP2 and egg yolk antibody), control4 (with BSA to replace VP2, or with Newcastle disease virus (NDV) to replace IBDV), and PBS was as background. S denotes scFv, N denotes control. BSA denotes VP2 was replaced by BSA.

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