PBS (pH 7.3) containing 1% stabilizing protein, 50% glycerol and 0.02% sodium azide.This antibody is supplied in a stabilized formulation. Compatibility with conjugation reactions depends on the chemistry of the conjugation method used. For conjugation me
Application Verdünnung:
WB 1:500~2000IHC 1:2000
Flow cytometric Analysis of Ramos cells
Flow cytometric Analysis of Jurkat cells
Immunohistochemical staining of paraffin-embedded Carcinoma of Human lung tissue using anti-CD79B mouse monoclonal antibody. (Heat-induced epitope retrieval by 1mM EDTA in 10mM Tris buffer (pH8.5) at 120AC for 3min
Immunohistochemical staining of paraffin-embedded Human lymph node tissue within the normal limits using anti-CD79B mouse monoclonal antibody. (Heat-induced epitope retrieval by 1mM EDTA in 10mM Tris buffer (pH8.5) at 120AC for 3min
Immunohistochemical staining of paraffin-embedded Human lymphoma tissue using anti-CD79B mouse monoclonal antibody. (Heat-induced epitope retrieval by 1mM EDTA in 10mM Tris buffer (pH8.5) at 120AC for 3min
Immunohistochemical staining of paraffin-embedded Human tonsil within the normal limits using anti-CD79B mouse monoclonal antibody. (Heat-induced epitope retrieval by 1mM EDTA in 10mM Tris buffer (pH8.5) at 120AC for 3min
HEK293T cells were transfected with the pCMV6-ENTRY control (Left lane) or pCMV6-ENTRY CD79B (Right lane) cDNA for 48 hrs and lysed. Equivalent amounts of cell lysates (5 ug per lane) were separated by SDS-PAGE and immunoblotted with anti-CD79B (1:2000).
Western blot analysis of extracts (35ug) from 2 different cell lines by using anti-CD79B monoclonal antibody (1:500).
Western blot analysis of extracts (35ug) from 5 different cell lines and human spleen tissue lysate by using anti-CD79A monoclonal antibody (1:500).
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