Full length human recombinant protein of human SNAI2 (NP_003059) produced in E.coli.
Boster Bio SNAI2 (SLUG) mouse monoclonal antibody, clone OTI1A6 (formerly 1A6). Catalog M01615-1. Tested in FC, IHC, WB. This antibody reacts with Human, Mouse, Rat.
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 1:1000IHC 1:150Flow Cytometry 1:100
HEK293T cells transfected with either SNAI2 (Myc-DDK-tagged) overexpress plasmid (Red) or empty vector control plasmid (Blue) were immunostained by anti-SNAI2 antibody (M01615-1)
Immunohistochemical staining of paraffin-embedded Carcinoma of Human lung tissue using anti-SNAI2 mouse monoclonal antibody. (Heat-induced epitope retrieval by 10mM citric buffer
Immunohistochemical staining of paraffin-embedded Carcinoma of Human thyroid tissue using anti-SNAI2 mouse monoclonal antibody. (Heat-induced epitope retrieval by 10mM citric buffer
Immunohistochemical staining of paraffin-embedded Adenocarcinoma of Human endometrium tissue using anti-SNAI2 mouse monoclonal antibody. (Heat-induced epitope retrieval by 10mM citric buffer
Figure from citation: Immunohistochemical analysis of Slug (also known as SNAI2) on serial sections of cartilage from normal and OA cartilage by using anti-SNAI2 antibody. Bar=100 um
Immunohistochemical staining of paraffin-embedded Carcinoma of Human bladder tissue using anti-SNAI2 mouse monoclonal antibody. (Heat-induced epitope retrieval by 10mM citric buffer
Immunohistochemical staining of paraffin-embedded Human lymphoma tissue using anti-SNAI2 mouse monoclonal antibody. (Heat-induced epitope retrieval by 10mM citric buffer
Immunohistochemical staining of paraffin-embedded Human Kidney tissue within the normal limits using anti-SNAI2 mouse monoclonal antibody. (Heat-induced epitope retrieval by 10mM citric buffer
HEK293T cells were transfected with the pCMV6-ENTRY control (Left lane) or pCMV6-ENTRY SNAI2 (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-SNAI2.
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