Product Information
Contents: Functional Grade Purified anti-human CD11a (LFA-1α)
Catalog Number: 16-0119
Sizes: 50 ug, 500 ug
Formulation: Phosphate buffer pH 7.2, 150 mM NaCl, No NaN3
Storage Conditions: Store at 4°C. Avoid repeated freeze/thaw cycles. KEEP CONTENTS STERILE.
Endotoxin Level: Less than 0.001 ng/ug antibody, as determined by the LAL assay.
Clone: HI111
Isotype: Mouse IgG1, κ
HLDA No.: IV N231
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Normal human peripheral blood stained with FG Purified HI111 and detected with FITC anti-mouse IgG (cat.no. 11-4011). Cells in the lymphocyte gate were analyzed.
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Description
The HI111 monoclonal antibody reacts with human CD11a, the 180 kDa integrin α
L, also known as the lymphocyte function associated antigen-1 (LFA-1) α chain. LFA-1, formed by non-covalent association of CD11a with CD18 (integrin β
2), serves as an important adhesion molecule involved in lymphocyte and granulocyte function. CD54 (ICAM-1), CD102 (ICAM-2), and CD50 (ICAM-3) are ligands for LFA-1. CD11a is expressed by all leukocytes.
Applications Reported
For research use only, not for diagnostic or therapeutic use. The HI111 antibody has been reported for use in flow cytometric analysis. It has also been reported in blocking of CD11a function in mixed lymphocyte reactions.
Applications Tested
The HI111 antibody has been tested by flow cytometric analysis of human peripheral blood leukocytes. This can be used at less than or equal to 1 μg per 100 μl blood (or per 1 million cells in 100 μl total staining volume). It is recommended that the antibody be carefully titrated for optimal performance in the assay of interest.
References
Kapsogeorgou EK, Dimitriou ID, Abu-Helu RF, Moutsopoulos HM, Manoussakis MN. Activation of epithelial and myoepithelial cells in the salivary glands of patients with Sjögren's syndrome: high expression of intercellular adhesion molecule-1 (ICAM.1) in biopsy specimens and cultured cells. Clin Exp Immunol. 2001 Apr;124(1):126-33. (
HI111, IHC frozen)
Knapp, W., B. Dorken, et al. eds 1989. Leucocyte Typing IV: White Cell Differentiation Antigens. Oxford University Press. New York.
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