The largest database of trusted experimental protocols

Senescence β galactosidase sa β gal staining kit

Manufactured by Beyotime
Sourced in China

The Senescence β-galactosidase (SA-β-gal) staining kit is a laboratory tool used to detect and quantify senescent cells. The kit provides a staining solution that allows for the visualization of β-galactosidase activity, which is a marker of cellular senescence. The core function of this kit is to enable researchers to identify and analyze senescent cells in their experiments.

Automatically generated - may contain errors

5 protocols using senescence β galactosidase sa β gal staining kit

1

Theabrown Cytotoxicity and Senescence Effects

Check if the same lab product or an alternative is used in the 5 most similar protocols
Theabrownin (> 90% of purity) was supplied by Theabio Co., Ltd (Hangzhou, China) (Batch number: 20181210001) and dissolved in the corresponding culture medium. Cis-platin (S116614) was purchased from Selleck (Shanghai, China) and dissolved in 50 °C warm water to 3 mg/ml and then diluted in cultured water to 15 µg/ml, according to the instruction. Fetal bovine serum (FBS), 0.25% trypsin Dulbecco’s modified eagle medium (DMEM) and Minimum Essential Medium α (MEM α), were obtained from Thermo Fisher Scientific (MA, USA). Annexin-V/FITC apoptosis detection kit was purchased from BD Biosciences (NJ, USA). Senescence β-galactosidase (SA-β-gal) staining kit was purchased from Beyotime (Shanghai, China). All antibodies were obtained from Cell Signaling Technology (MA, USA).
+ Open protocol
+ Expand
2

Senescence and Chondrocyte Visualization

Check if the same lab product or an alternative is used in the 5 most similar protocols
The senescence β‐galactosidase (SA‐β‐Gal) staining kit (Beyotime, cat. no. C0602, China) was used to detect senescent chondrocytes according to the manufacturer's instructions. We observed SA‐β‐Gal cells using an inverted phase contrast microscope (Lecia, Germany). Total cells and SA‐β‐Gal‐positive cells were counted per culture dish.
Cells or tissues were incubated with 1% Alcian blue solution for 1 h. After incubation, cells or tissues were washed twice with PBS. An inverted phase‐contrast microscope (Leica, Germany) was used to obtain representative images.
+ Open protocol
+ Expand
3

Senescence Quantification using SA-β-gal Assay

Check if the same lab product or an alternative is used in the 5 most similar protocols
Senescence was measured using a Senescence β‑galactosidase (SA-β-gal) Staining Kit (C0602, Beyotime Biotechnology, China) according to the manufacturer’s instructions. For cell assay, HUVECs were fixed with 2% formaldehyde for 10 min at room temperature. After washing with PBS twice, cells were incubated with fresh SA-β-gal staining solution at 37 °C overnight. The percentage of SA-β-gal-positive cells was calculated through counting the positively stained cells. For tissue assay, the frozen sections were prepared to stain according to the kit instruction of SA-β-gal and the images were observed under an Olympus BX43 microscope (Olympus).
+ Open protocol
+ Expand
4

Senescence Assay in Cell Cultures

Check if the same lab product or an alternative is used in the 5 most similar protocols
Cells were seeded on 6-well plates. Senescence staining was performed using a Senescence β-Galactosidase (SA-β-Gal) Staining Kit (Beyotime) according to the manufacturer’s instructions.
+ Open protocol
+ Expand
5

Senescence-β-Galactosidase Staining Assay

Check if the same lab product or an alternative is used in the 5 most similar protocols
The Senescence-β-Galactosidase (SA-β-Gal) Staining Kit (Beyotime Institute of Biotechnology, Shanghai, China) was used to detect cell aging. According to the manufacturer’s instructions, 1 × 105 cells were fixed for 10 min with fixative solution at room temperature, with PBS washing three times. Then, cells were incubated in SA-β-Gal–staining solution for 12 h at 37 °C at pH 6.0 without CO2 in darkness. The SA-β-Gal–positive cells were dyed blue-green. For quantification purposes, at least 400 cell fields were scored for staining in five random microscopy fields, and the percentage of positive cells in each group was calculated.
+ 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!