Anti-CD8 alpha antibody [YTS169.4] - BSA and Azide free (ab230292)
Key features and details
- Rat monoclonal [YTS169.4] to CD8 alpha - BSA and Azide free
- Suitable for: Flow Cyt
- Reacts with: Mouse
- Isotype: IgG2b
Overview
-
Product name
Anti-CD8 alpha antibody [YTS169.4] - BSA and Azide free
See all CD8 alpha primary antibodies -
Description
Rat monoclonal [YTS169.4] to CD8 alpha - BSA and Azide free -
Host species
Rat -
Tested Applications & Species
See all applications and species dataApplication Species Flow Cyt Mouse -
Immunogen
The details of the immunogen for this antibody are not available.
-
Positive control
- Flow Cyt: Mouse spleen cells.
-
General notes
Properties
-
Form
Liquid -
Storage instructions
Shipped at 4°C. Store at +4°C. Do Not Freeze. -
Storage buffer
Constituent: PBS -
Carrier free
Yes -
Concentration information loading...
-
Purity
IgG fraction -
Clonality
Monoclonal -
Clone number
YTS169.4 -
Isotype
IgG2b -
Research areas
Images
-
Overlay histogram showing mouse spleen cells (C57BL/6) labeling CD8 alpha with ab22378 (red line). The cells were incubated in 1x PBS / 10% normal goat serum / 0.3M glycine to block non-specific protein-protein interactions. The cells were then incubated with the antibody (ab22378, 0.1μg/1x106 cells) for 30 min at 4ºC. The secondary antibody used was Alexa Fluor® 488 goat anti-rat IgG (H&L) (ab150157) at 1/2000 dilution for 30 min at 4ºC. Isotype control antibody (black line) was rat IgG2b [RTK4530] (ab18541, 2μg/1x106 cells) used under the same conditions.
Acquisition of >5,000 events were collected using a 20mW Argon ion laser (488nm) and 525/30 bandpass filter.
This data was developed using the same antibody clone in a different buffer formulation containing PBS, L-Arginine and sodium azide (ab22378).
-
Normal mouse (CBA) spleen cells (red cell lysed) double stained with ab22378 (0.3 µg/mL, detected with Alexa Fluor® 488-conjugated monoclonal mouse anti-rat antibody) and an APC conjugated hamster anti-mouse CD3 antibody. ab22378 stains an expected subpopulation of CD8 alpha positive T cells.
This data was developed using the same antibody clone in a different buffer formulation containing PBS, L-Arginine and sodium azide (ab22378).