M10AR
antibody from Invitrogen Antibodies
Targeting: IL2RA
CD25, IDDM10, IL2R
Antibody data
- Antibody Data
- Antigen structure
- References [2]
- Comments [0]
- Validations
- Immunocytochemistry [1]
- Flow cytometry [1]
- Other assay [1]
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Validation data
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- Product number
- M10AR - Provider product page
- Provider
- Invitrogen Antibodies
- Product name
- Anti-CD25 Monoclonal Antibody (2R12)
- Antibody type
- Monoclonal
- Antigen
- Other
- Description
- M10AR targets CD25 in ICC/IF, FACS, IHC, IP, and WB applications and shows reactivity with Human samples. The M10AR immunogen is p55 alpha chain of the human IL-2 receptor. M10AR detects CD25 which has a predicted molecular weight of approximately 28 kDa.
- Reactivity
- Human
- Host
- Mouse
- Isotype
- IgG
- Antibody clone number
- 2R12
- Vial size
- 100 tests
- Concentration
- 20 µg/ml
- Storage
- 4° C
Submitted references Heterogeneous immunophenotype of granular lymphocyte expansions: differential expression of the CD8 alpha and CD8 beta chains.
Structural and functional characterization of IL 2 receptors on activated human B cells.
de Totero D, Tazzari PL, DiSanto JP, di Celle PF, Raspadori D, Conte R, Gobbi M, Ferrara GB, Flomenberg N, Lauria F
Blood 1992 Oct 1;80(7):1765-73
Blood 1992 Oct 1;80(7):1765-73
Structural and functional characterization of IL 2 receptors on activated human B cells.
Boyd AW, Fisher DC, Fox DA, Schlossman SF, Nadler LM
Journal of immunology (Baltimore, Md. : 1950) 1985 Apr;134(4):2387-92
Journal of immunology (Baltimore, Md. : 1950) 1985 Apr;134(4):2387-92
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Supportive validation
- Submitted by
- Invitrogen Antibodies (provider)
- Main image
- Experimental details
- Immunofluorescent analysis of CD25 (green) showing staining in the cytoplasm of Jurkat cells (right) compared to a negative control without primary antibody (left). Formalin-fixed cells were permeabilized with 0.1% Triton X-100 in TBS for 5-10 minutes and blocked with 3% BSA-PBS for 30 minutes at room temperature. Cells were probed with a CD25 monoclonal antibody (Product # M10AR) in 3% BSA-PBS at a dilution of 1:20 and incubated overnight at 4ºC in a humidified chamber. Cells were washed with PBST and incubated with a DyLight-conjugated secondary antibody in PBS at room temperature in the dark. F-actin (red) was stained with a fluorescent red phalloidin and nuclei (blue) were stained with Hoechst or DAPI. Images were taken at a magnification of 60x.
Supportive validation
- Submitted by
- Invitrogen Antibodies (provider)
- Main image
- Experimental details
- Flow cytometry analysis of CD25 in Jurkat cells (green) compared to an isotype control (blue). Cells were harvested, adjusted to a concentration of 1-5x10^6 cells/ml, fixed with 2% paraformaldehyde and washed with PBS. Cells were blocked with a 2% solution of BSA-PBS for 30 min at room temperature and incubated with a CD25 monoclonal antibody (Product # M10AR) at a dilution of 1:10 for 60 min at room temperature. Cells were then incubated for 40 min at room temperature in the dark using a Dylight 488-conjugated secondary antibody and re-suspended in PBS for FACS analysis.
Supportive validation
- Submitted by
- Invitrogen Antibodies (provider)
- Main image
- Experimental details
- IP-MS enrichment of IL2RA (LFQ intensity): IL2RA was enriched 2108-fold from SR lysate compared to background proteins, using the optimized IP-MS workflow with Pierce MS-Compatible Magnetic IP Kit protein A/G (Product # 90409) and IL2RA antibody (Product # M10AR). The STRING database (www.string-db.org) was used to identify the protein interactor list. See more information on IP-MS verification of antibody selectivity.