Anti-CD18 antibody [MEM-48] - Low endotoxin, Azide free
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(1 Publication)
- Flow Cyt
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Flow Cytometry - Anti-CD18 antibody [MEM-48] - Low endotoxin, Azide free (AB46700)
Overlay histogram showing peripheral blood lymphocytes stained with ab46700 (red line). The cells were incubated with the antibody (ab46700, 1μg/1x106 cells) for 30 min at 4°C. The secondary antibody used was DyLight® 488 goat anti-mouse IgG (H&L) (ab96879) at 1/200 dilution for 30 min at 4°C. Isotype control antibody (black line) was mouse IgG1 [ICIGG1] (ab91353, 2μg/1x106 cells) used under the same conditions. Acquisition of >5,000 events was performed gating on peripheral blood lymphocytes.
- Flow Cyt
Supplier Data
Flow Cytometry - Anti-CD18 antibody [MEM-48] - Low endotoxin, Azide free (AB46700)
Separation of human leukocytes (red-filled) from CD18 negative blood debris (black-dashed) in flow cytometry analysis (surface staining) of human peripheral whole blood stained using ab46700 (concentration in sample 1 μg/ml).
- Flow Cyt
Supplier Data
Flow Cytometry - Anti-CD18 antibody [MEM-48] - Low endotoxin, Azide free (AB46700)
Flow cytometry surface staining pattern of human peripheral whole blood stained using ab46700 (concentration in sample 1 μg/ml).
- WB
Supplier Data
Western blot - Anti-CD18 antibody [MEM-48] - Low endotoxin, Azide free (AB46700)
The reactivity of MEM-48 antibody was assessed by comparing binding signals in a panel of various human cell samples. Western blotting analysis was performed on RIPA buffer extracts of THP-1, Kg1a, U937, HPB-ALL, Raji, Jurkat, leukocytes, and HeLa cells, mixed and heated (100°C, 5 min) with reducing (2-mercaptoethanol) SDS-loading buffer. Samples were resolved using 10% SDS-PAGE gel.
Nitrocellulose membrane blot was probed with ab46700 (2 µg/ml), followed by IRDye 800CW Goat-anti-Mouse IgG (green). For multiplex fluorescent Western blot detection, mouse anti-GAPDH monoclonal antibody FF26A conjugated with DyLight 680 (0.1 µg/ml) was used as the loading control (red).
CD18 was detected at ~90-100 kDa in the respective cell lines.
All lanes:
Western blot - Anti-CD18 antibody [MEM-48] - Low endotoxin, Azide free (ab46700) at 2 µg/mL
Lane 1:
THP-1
Lane 2:
Kg1a
Lane 3:
U937
Lane 4:
HPB-ALL
Lane 5:
Raji
Lane 6:
Jurkat
Lane 7:
Leukocytes
Lane 8:
HeLa
Secondary
All lanes:
IRDye 800CW Goat-anti-Mouse IgG
Observed band size: 90-100 kDa
false
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Reactivity data
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Supplementary information
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Biological function summary
The CD18 protein functions in conjunction with associated alpha subunit partners forming a part of the wider integrin family complex. ItgB2 as it is sometimes referred to is essential for cell adhesion processes. These heterodimers facilitate binding between leukocytes and various ligands on endothelial cells which subsequently controls leukocyte transmigration through vascular walls. CD18's activities are critical in immune system responses making it a prominent focus in immunological research.
Pathways
The role of CD18 extends into inflammatory and immune response signaling pathways. It contributes critically to the leukocyte adhesion cascade. This cascade engagement involves interaction with other proteins such as ICAM-1 on endothelial surfaces. CD18 through its association in integrin-mediated signaling influences processes like phagocytosis and lymphocyte activation giving it a central place in cellular immunity.
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Publications (1)
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Blood 113:358-69 PubMed18922855
2008
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