Flow cytometric analysis of THP-1 (Human monocytic leukemia monocyte, Left) / Jurkat (Human T cell leukemia T lymphocyte, Right) labelling NA/LE Mouse anti-human CD28 mAb
(S0B0010) (Red) compared with a Mouse monoclonal IgG (Black) isotype control and an unlabelled control (cells without incubation with primary antibody and secondary antibody) (Blue). Goat Anti-Mouse IgG (H+L) (min X Hu, Bov, Hrs Sr Prot) (Alexa Fluor® 647 Conjugate) at 1/2000 was used as the secondary antibody. Negative control: THP-1
Product Details
Product Details
Product Specification
Host | Goat |
Antigen | Mouse IgG |
Antibody Type | Polyclonal antibody |
Application | ICC, IF |
Reactivity | Ms |
Purification | Immunogen Affinity |
Concentration | 2 mg/ml |
Conjugation | Alexa Fluor® 647 |
Physical Appearance | Liquid |
Storage Buffer | PBS, 25% Glycerol, 1% BSA, 0.3% Proclin 300 |
Stability & Storage | 12 months from date of receipt / reconstitution, 2 to 8 °C as supplied. |
Dilution
application | dilution | species |
ICC | 1:500 | Ms |
IF | 1:500 | Ms |
Background
This antibody has been tested to ensure minimal cross-reaction with human, Bovine, Horse serum proteins.
Picture
Picture
FC
Immunofluorescence
IF shows positive staining in paraffin-embedded human esophagus. Anti- CD44V6 antibody(S0B0614) was used at 1/500 dilution (magenta) and incubated overnight at 4°C. Goat Anti-Mouse IgG (H+L) (min X Hu, Bov, Hrs Sr Prot) (Alexa Fluor® 647 Conjugate) was used as secondary antibody at 1/500 dilution. Counterstained with DAPI (Blue). Heat mediated antigen retrieval with EDTA buffer pH9.0 was performed before commencing with IF staining protocol.
IF shows positive staining in paraffin-embedded human prostate. Anti- CD44V6 antibody(S0B0614) was used at 1/500 dilution (magenta) and incubated overnight at 4°C. Goat Anti-Mouse IgG (H+L) (min X Hu, Bov, Hrs Sr Prot) (Alexa Fluor® 647 Conjugate) was used as secondary antibody at 1/500 dilution. Counterstained with DAPI (Blue). Heat mediated antigen retrieval with EDTA buffer pH9.0 was performed before commencing with IF staining protocol.
