anti human fd goat polyclonal antibody (R&D Systems)
Structured Review

Anti Human Fd Goat Polyclonal Antibody, supplied by R&D Systems, used in various techniques. Bioz Stars score: 94/100, based on 10 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/anti+human+fd+goat+polyclonal+antibody/pm29450541-82-6-12?v=R%26D+Systems
Average 94 stars, based on 10 article reviews
Images
1) Product Images from "Induction of Ocular Complement Activation by Inflammatory Stimuli and Intraocular Inhibition of Complement Factor D in Animal Models."
Article Title: Induction of Ocular Complement Activation by Inflammatory Stimuli and Intraocular Inhibition of Complement Factor D in Animal Models.
Journal: Investigative ophthalmology & visual science
doi: 10.1167/iovs.17-22605
Figure Legend Snippet: FIGURE 6. Intravitreal administration of an antibody against complement factor D inhibits LPS-induced Ba generation in rabbits in the posterior segment of the eye, but not systemically or in the anterior segment of the eye. (A) MAC deposition after Zymosan-induced alternative pathway activation in 6% human serum (solid line) or rabbit serum (dotted line) was blocked by a FD-neutralizing polyclonal antibody with IC50 values of 8.1 and 4.9 nM, respectively. Twenty-four hours before LPS challenge, goat IgG or anti-FD was delivered IVT at 200 lg per eye to both eyes. Eighteen hours after intravenous injection of either PBS or LPS at 20 lg/kg, plasma (D) and eye tissue were collected. Eyes were dissected immediately into vitreous humor (B), retina/RPE/choroid (C), aqueous humor (E), and iris/ciliary (CB) (F). Complement Ba levels in indicated tissues were measured by Western blot and graphed relative to the IgG/PBS control group. LPS-induced Ba generation was inhibited 100% (P < 0.01) in vitreous humor and was reduced by 60% (P < 0.01) of PBS control levels in retina/RPE/choroid. The rabbit LPS study is a representative of two independent studies.
Techniques Used: Activation Assay, Injection, Clinical Proteomics, Western Blot, Control