Mouse Monoclonal CD2 antibody. Carrier free. Suitable for Flow Cyt, WB and reacts with Human samples. Immunogen corresponding to Full Length Protein corresponding to Human CD2.
Constituents: 100% PBS
Flow Cyt | WB | |
---|---|---|
Human | Tested | Tested |
Species | Dilution info | Notes |
---|---|---|
Species Human | Dilution info - | Notes ab170190 - Mouse monoclonal IgG1, is suitable for use as an isotype control with this antibody. |
Species | Dilution info | Notes |
---|---|---|
Species Human | Dilution info 0.50000-2.00000 µg/mL | Notes - |
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CD2 interacts with lymphocyte function-associated antigen CD58 (LFA-3) and CD48/BCM1 to mediate adhesion between T-cells and other cell types. CD2 is implicated in the triggering of T-cells, the cytoplasmic domain is implicated in the signaling function.
CD2, SRBC, T-cell surface antigen CD2, Erythrocyte receptor, LFA-2, LFA-3 receptor, Rosette receptor, T-cell surface antigen T11/Leu-5
Mouse Monoclonal CD2 antibody. Carrier free. Suitable for Flow Cyt, WB and reacts with Human samples. Immunogen corresponding to Full Length Protein corresponding to Human CD2.
Constituents: 100% PBS
Does not work with Rat in Western Blot applications
Purified IgG from mouse ascites fluid.
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CD2 also known as T11 or LFA-2 acts as a cell surface glycoprotein expressed mainly on T-cells natural killer cells and thymocytes. This protein has a molecular mass of approximately 50-55 kDa. CD2 plays a critical role in facilitating cell-cell adhesion and signal transduction. It serves as a receptor for the CD58 ligand on antigen-presenting cells supporting the interaction between T-cells and these cells. By enhancing adhesion CD2 contributes to the formation of the immunological synapse necessary for effective immune response.
The functioning of CD2 helps in the modulation of immune responses and T-cell activation. CD2 participates in signal transduction leading to cytokine production and proliferation. It is associated with the immunological synapse complex working closely with other surface molecules like Lck and CD3 to promote T-cell responses. This collaboration is vital for the development and function of immune cells driving adaptive immunity.
CD2 engages in pathways integral to T-cell activation and signal transduction. A well-known pathway involving CD2 is the TCR (T-cell Receptor) signaling pathway where it partners with CD3 to initiate T-cell activation. Additionally CD2 influences the LAT (Linker for Activation of T-cells) pathway contributing to downstream signaling cascades that involve various signaling proteins such as Lck and ZAP-70 ensuring proper T-cell function.
CD2 shows connections to autoimmune diseases and cancers. For instance its involvement in abnormal T-cell activation links CD2 to autoimmune conditions like rheumatoid arthritis. Also various leukemias demonstrate altered CD2 expression suggesting a role in cancer pathogenesis. Through these disease states CD2's interaction with the CD58 protein becomes critical as this interaction affects the activity of T-cells in the disease milieu influencing disease progression and treatment outcomes.
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We have not tested this specific species and application combination in-house, but expect it will work. It is covered by our product promise.
This species and application combination has not been tested, but we predict it will work based on strong homology. However, this combination is not covered by our product promise.
We do not recommend this combination. It is not covered by our product promise.
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Flow cytometric analysis of Jurkat cells labeling CD2 with ab175287 at a dilution of 0.5 μg/test (green), compared to an isotype control (blue). A Dylight 488-conjugated goat anti-mouse IgG (H+L) was used as the secondary antibody.
All lanes: Western blot - Anti-CD2 antibody [TS218] - BSA and Azide free (ab175287) at 2 µg/mL
Lane 1: Ramos at 30 µg
Lane 2: A-431 at 30 µg
Lane 3: K562 at 30 µg
Lane 4: Raji at 30 µg
All lanes: Goat anti-Mouse IgG (H+L) Secondary Antibody, HRP conjugate at 1/4000 dilution
Predicted band size: 39 kDa
Flow cytometric analysis of PBMC cells labeling CD2 with ab175287 at a dilution of 0.5 μg/test (green), compared to an isotype control (blue). A Dylight 488-conjugated goat anti-mouse IgG (H+L) was used as the secondary antibody.
Flow cytometric analysis of PBMC cells labeling CD2 with ab175287 at a dilution of 0.5 μg/test (green), compared to an isotype control (blue). A Dylight 488-conjugated goat anti-mouse IgG (H+L) was used as the secondary antibody.
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