The largest database of trusted experimental protocols

4 protocols using ab8227

1

Western Blot Analysis of Matrix and Senescence Markers

Check if the same lab product or an alternative is used in the 5 most similar protocols
Protein expression of matrix-related molecules (aggrecan and collagen II) and senescence-related molecules (p16 and p53), and activity of the p38 pathway were analyzed by Western blot assay. Briefly, total protein was extracted by RIPA lysis buffer (Beyotime, China) and its concentration was measured by the Protein BCA Kit (Beyotime, China). Then, 60 μg protein in each group was separated by SDS/polyacrylamide gel (SDS/PAGE) and transferred to the PVDF membrane (Beyotime, China). Subsequently, the PVDF membranes were incubated with primary antibodies (β-actin: Abcam, ab8227; p16: Novus, NBP2-37740; p53: Abcam, ab26; aggrecan: Norvus, NB120-11579; collagen II: Abcam, ab185430; p38: Cell Signaling Technology, #8690; p-p38: Cell Signaling Technology, #4511) and horseradish peroxidase (HRP)–conjugated secondary antibodies (Beyotime, China). Finally, the protein bands on the PVDF membrane were visualized by SuperSignal West Pico Trial Kit (Thermo, U.S.A.). The density of each protein band was quantitated using Quantity One Software.
+ Open protocol
+ Expand
2

Western Blot Antibody Panel for Iron Regulation

Check if the same lab product or an alternative is used in the 5 most similar protocols
The following antibodies were used for Western blot analysis: anti-EIF3B (Bethyl A301-761A) at 1:1000; anti-FTL (Abcam, ab69090) at 1:800; anti-FTH (Santa Cruz, sc-25617) at 1:400; anti-IRP1 (Abbexa, abx004618) at 1:400; anti-IRP2 (Abcam, ab129069) at 1:800; and anti-b-Actin (Abcam, ab8227) at 1:1000, anti-Ferroportin (Novus, NBP 1–2150255) at 1:300.
+ Open protocol
+ Expand
3

Western Blot Analysis of Retinal Proteins

Check if the same lab product or an alternative is used in the 5 most similar protocols
Cell pellets were extracted by the M-PER mammalian protein extraction reagent (Thermo Fisher Scientific, 78501) supplemented with proteinase inhibitors (Roche, 04693159001), and the protein concentration was quantified by a Bio-Rad protein reader. After denaturing at 95°C for 5 min, the samples (20 μg) were run on 4–15% gradient SDS-PAGE gel at room temperature, and wet transferred onto nitrocellulose membrane at 4°C. The membranes were incubated in blocking buffer containing 5% (w/v) non-fat milk for 1 hr at room temperature and subsequently incubated overnight at 4°C in blocking buffer supplemented with primary antibody. Primary antibodies against the following proteins were used: CRALBP (1:500 Abcam, ab15051), RPE65 (1:1,000 Novus Biologicals, NB100-355), β-Actin (1:2,000 Abcam, ab8227), BEST1 (1:500 Novus Biologicals, NB300-164), His (1:1,000 Fisher Scientific, PA1983B), and Myc (1:1,000 Fisher Scientific, PA1981). Fluorophore-conjugated mouse and rabbit secondary antibodies (LI-COR Biosciences, 925–68070 and 925–32213, respectively) were used at a concentration of 1:10,000 and an incubation time of 1 hr at room temperature, followed by infrared imaging.
+ Open protocol
+ Expand
4

Western Blot Analysis of Retinal Proteins

Check if the same lab product or an alternative is used in the 5 most similar protocols
Cell pellets were extracted by the M-PER mammalian protein extraction reagent (Thermo Fisher Scientific, 78501) or Mem-PER Plus membrane protein extraction kit (Thermo Fisher Scientific, 89842) with proteinase inhibitors (Roche, 04693159001), and the protein concentration was quantified by a Bio-Rad protein reader. After denaturing at 95 °C for 5 min, the samples (20 μg) were run on 4–15% gradient SDS-PAGE gel at room temperature, and wet transferred onto nitrocellulose membrane at 4 °C. The membranes were incubated in blocking buffer containing 5% (w/v) non-fat milk for 1 hour at room temperature, and subsequently incubated overnight at 4 °C in blocking buffer supplemented with primary antibody. Primary antibodies against the following proteins were used for immunoblotting: CRALBP (1:500 Abcam, ab15051), RPE65 (1:1,000 Novus Biologicals, NB100-355), β-actin (1:2,000 Abcam, ab8227), BESTROPHIN-1 (1:500 Novus Biologicals, NB300-164), His (1:1,000 Fisher Scientific, PA1983B) and Myc (1:1,000 Fisher Scientific, PA1981). Fluorophore-conjugated mouse and rabbit secondary antibodies (LI-COR Biosciences, 925–68070 and 925–32213, respectively) were used at a concentration of 1:10,000 and an incubation time of 1 h at room temperature, followed by infrared imaging.
+ Open protocol
+ Expand

About PubCompare

Our mission is to provide scientists with the largest repository of trustworthy protocols and intelligent analytical tools, thereby offering them extensive information to design robust protocols aimed at minimizing the risk of failures.

We believe that the most crucial aspect is to grant scientists access to a wide range of reliable sources and new useful tools that surpass human capabilities.

However, we trust in allowing scientists to determine how to construct their own protocols based on this information, as they are the experts in their field.

Ready to get started?

Sign up for free.
Registration takes 20 seconds.
Available from any computer
No download required

Sign up now

Revolutionizing how scientists
search and build protocols!