LFA-2 Antibody Recombinant Mouse mAb / CD2 [clone rLFA2/8516] (V4656)
 Catalog No.  Formulation  Size
V4656-100UG
0.2 mg/ml in 1X PBS with 0.1 mg/ml BSA (US sourced), 0.05% sodium azide
100 ug
V4656-20UG
0.2 mg/ml in 1X PBS with 0.1 mg/ml BSA (US sourced), 0.05% sodium azide
20 ug
V4656SAF-100UG
1 mg/ml in 1X PBS; BSA free, sodium azide free
100 ug
./plp/all_image/img-V4656-100UG-1.jpg ./plp/all_image/img-V4656-100UG-2.jpg ./plp/all_image/img-V4656-100UG-3.jpg
Bulk quote request
Availability 1-3 business days
Species Reactivity Human
Format Purified
Host Mouse
Clonality Recombinant Mouse Monoclonal
Isotype Mouse IgG1, kappa
Clone Name rLFA2/8516
Purity Protein A/G affinity
UniProt P06729
Localization Cell surface
Applications Immunohistochemistry (FFPE) : 1-2ug/ml for 30 min at RT
Limitations This LFA-2 antibody is available for research use only.
Immunohistochemistry analysis of LFA-2 antibody (clone rLFA2/8516) in human tonsil tissue. Formalin-fixed, paraffin-embedded tonsil shows strong membranous HRP-DAB brown staining in interfollicular T lymphocytes, consistent with CD2 expression on mature T cells. Germinal center regions display comparatively reduced staining, highlighting the expected distribution of T cell populations within lymphoid tissue. Hematoxylin counterstain clearly delineates nuclear morphology and overall tonsillar architecture. The inset shows PBS used in place of primary antibody as a negative control, confirming absence of non-specific secondary antibody binding. Heat-induced epitope retrieval was performed by boiling tissue sections in 10 mM Tris with 1 mM EDTA, pH 9.0, for 20 minutes followed by cooling prior to staining.
Immunohistochemistry analysis of LFA-2 antibody (clone rLFA2/8516) in human tonsil tissue. Formalin-fixed, paraffin-embedded tonsil shows strong membranous HRP-DAB brown staining in interfollicular T lymphocytes, consistent with CD2 expression on mature T cells. Germinal center regions display comparatively reduced staining, highlighting the expected distribution of T cell populations within lymphoid tissue. Hematoxylin counterstain clearly delineates nuclear morphology and overall tonsillar architecture. The inset shows PBS used in place of primary antibody as a negative control, confirming absence of non-specific secondary antibody binding. Heat-induced epitope retrieval was performed by boiling tissue sections in 10 mM Tris with 1 mM EDTA, pH 9.0, for 20 minutes followed by cooling prior to staining.
IHC staining of FFPE human tonsil tissue with recombinant LFA-2 antibody (clone rLFA2/8516) HIER: boil tissue sections in pH 9 10mM Tris with 1mM EDTA for 20 min and allow to cool before testing.
IHC staining of FFPE human tonsil tissue with recombinant LFA-2 antibody (clone rLFA2/8516) HIER: boil tissue sections in pH 9 10mM Tris with 1mM EDTA for 20 min and allow to cool before testing.
SDS-PAGE analysis of purified, BSA-free recombinant LFA-2 antibody (clone rLFA2/8516) as confirmation of integrity and purity.
SDS-PAGE analysis of purified, BSA-free recombinant LFA-2 antibody (clone rLFA2/8516) as confirmation of integrity and purity.