Figure - PMC

Skip to main content

An official website of the United States government

Here's how you know

Here's how you know

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you've safely connected to the .gov website. Share sensitive information only on official, secure websites.

View full-text article in PMC

. 2020 Nov 12;15:8875–8892. doi: 10.2147/IJN.S270208

Search in PMC
Search in PubMed
View in NLM Catalog
Add to search

© 2020 Lu et al.

This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).

PMC Copyright notice

Binding affinity of TAT-AT7 to VEGFR-2 and NRP-1. The binding curves for AT7, TAT, and TAT-AT7 with the recombinant proteins VEGFR-2 (A) and NRP-1 (B) were assessed by SPR analysis. Different peptides at a series of concentrations (increasing from 0.0156 μM to 0.03125 μM, 0.0625 μM, 0.125 μM, and 0.25 μM) were flowed over the surface of chip-immobilized VEGFR-2 or NRP-1 proteins. The K_D value reflects the level of analyte binding to ligand proteins.