FITC Anti-TCR gamma + TCR delta antibody [5A6.E91] (ab171110)
Key features and details
- FITC Mouse monoclonal [5A6.E91] to TCR gamma + TCR delta
- Suitable for: Flow Cyt
- Reacts with: Human, Non human primates
- Conjugation: FITC. Ex: 493nm, Em: 528nm
- Isotype: IgG1
Overview
-
Product name
FITC Anti-TCR gamma + TCR delta antibody [5A6.E91]
See all TCR gamma + TCR delta primary antibodies -
Description
FITC Mouse monoclonal [5A6.E91] to TCR gamma + TCR delta -
Host species
Mouse -
Conjugation
FITC. Ex: 493nm, Em: 528nm -
Tested Applications & Species
See all applications and species dataApplication Species Flow Cyt Human -
Immunogen
Full length protein corresponding to Human TCR gamma + TCR delta.
Properties
-
Form
Liquid -
Storage instructions
Shipped at 4°C. Store at +4°C short term (1-2 weeks). Upon delivery aliquot. Store at -20°C long term. Avoid freeze / thaw cycle. Store In the Dark. -
Storage buffer
Preservative: 0.1% Sodium azide
Constituents: PBS, 0.5% BSA, Glycerol (glycerin, glycerine) -
Concentration information loading...
-
Purity
Protein A purified -
Clonality
Monoclonal -
Clone number
5A6.E91 -
Isotype
IgG1 -
Research areas
Images
-
Flow cytometry analysis of TCR gamma + TCR delta showing positive staining in the membrane of peripheral blood mononuclear cells compared to an isotype control (blue). Human blood was collected and combined with a hydrophilic polysaccharide then centrifuged. Samples transferred to a conical tube and washed with PBS. 50 ul of cell solution was added to each tube at a dilution of 2x10^7 cells/ml and 50 ul of isotype control and ab171110 at 1:20 added. Cells were incubated for 30 min at 4°C and washed with a cell buffer and incubated with a DyLight 488-conjugated goat anti-mouse IgG (H+L) secondary for 30 min at 4°C in the dark. FACS analysis was performed using 400 ul of cell buffer.
-
Flow cytometry analysis of TCR gamma + TCR delta showing positive staining in the membrane of peripheral blood mononuclear cells compared to an isotype control (blue). Human blood was collected and combined with a hydrophilic polysaccharide then centrifuged. Samples were transferred to a conical tube and washed with PBS. 50 ul of cell solution was added to each tube at a dilution of 2x10^7 cells/ml and 50 ul of isotype control and ab171110 at 1:20 added. Cells were incubated for 30 min at 4°C and washed with a cell buffer and incubated with a DyLight 488-conjugated goat anti-mouse IgG (H+L) secondary for 30 min at 4°C in the dark. FACS analysis was performed using 400 ul of cell buffer.