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Read our guarantee »Products:Signal Transduction >> Protein Phosphorylation >> Tyrosine Kinases >> Other
Anti-BMX antibody
See all BMX products (8) ...
Rabbit polyclonal to BMX
ab59360 detects endogenous levels of total BMX protein.
ELISA, ICC/IF, WB, IHC-Pmore details
Reacts with
Human
Predicted to work with
Mouse
Synthesized non phosphopeptide derived from human BMX around the phosphorylation site of tyrosine 566 (DQYPVS).
A549 cytoplasmic lysate (WB) Human thyroid gland tissue (IHC)
Liquid
Shipped at 4°C. Upon delivery aliquot and store at -20°C. Avoid freeze / thaw cycles.
Preservative: 0.02% Sodium Azide
Constituents: 50% Glycerol, PBS (without Mg2+ and Ca2+), 150mM Sodium chloride, pH 7.4
Concentration information loading...
Immunogen affinity purified
Purified from rabbit antiserum by affinity chromatography, using epitope specific immunogen.
Polyclonal
IgG
Signal Transduction >> Protein Phosphorylation >> Tyrosine Kinases >> Other
Our Abpromise guarantee covers the use of ab59360 in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
ELISA: 1/10000
ICC/IF: Use at an assay dependent dilution.
WB: 1/500 - 1/1000.Detects a band of approximately 78 kDa.
IHC-P: 1/50 - 1/100.
Activity is required for interleukin 6 (IL-6) induced differentiation. May play a role in the growth and differentiation of hematopoietic cells. May be involved in signal transduction in endocardial and arterial endothelial cells.
Preferentially expressed in epithelial and endothelial cells.
Belongs to the protein kinase superfamily. Tyr protein kinase family. TEC subfamily.
Contains 1 Btk-type zinc finger.
Contains 1 PH domain.
Contains 1 protein kinase domain.
Contains 1 SH2 domain.
SH2 domain mediates interaction with RUFY1.
Cytoplasm.
Target information above from: UniProt accessionP51813
The UniProt Consortium
The Universal Protein Resource (UniProt) in 2010
Nucleic Acids Res. 38:D142-D148 (2010).
Western blot - BMX antibody (ab59360)

All lanes : Anti-BMX antibody (ab59360) at 1/500 dilution
Lane 1 : Extracts from A549 cells with no immunizing peptide
Lane 2 : Extracts from A549 cells with immunizing peptide
Observed band size : 78 kDa (why is the actual band size different from the predicted?)
Immunohistochemistry (Paraffin-embedded sections) - BMX antibody (ab59360)

ab59360, at a 1/50 dilution, staining human BMX in thyroid gland, using Immunohistochemistry, Paraffin embedded tissue, in the absence of the immunizing peptide (left image) and in the presence of the immunizing peptide (right image).
Immunocytochemistry/ Immunofluorescence-BMX antibody(ab59360)

ICC/IF image of ab59360 stained HeLa cells. The cells were 4% PFA fixed (10 min) and then incubated in 1%BSA / 10% normal goat serum / 0.3M glycine in 0.1% PBS-Tween for 1h to permeabilise the cells and block non-specific protein-protein interactions. The cells were then incubated with the antibody (ab59360, 1µg/ml) overnight at +4°C. The secondary antibody (green) was Alexa Fluor® 488 goat anti-rabbit IgG (H+L) used at a 1/1000 dilution for 1h. Alexa Fluor® 594 WGA was used to label plasma membranes (red) at a 1/200 dilution for 1h. DAPI was used to stain the cell nuclei (blue) at a concentration of 1.43µM.
This product has been referenced in:
See 1 publication for this product
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All lanes : Anti-BMX antibody (ab59360) at 1/500 dilution
Lane 1 : Extracts from A549 cells with no immunizing peptide
Lane 2 : Extracts from A549 cells with immunizing peptide
Observed band size : 78 kDa (why is the actual band size different from the predicted?)

ab59360, at a 1/50 dilution, staining human BMX in thyroid gland, using Immunohistochemistry, Paraffin embedded tissue, in the absence of the immunizing peptide (left image) and in the presence of the immunizing peptide (right image).

ICC/IF image of ab59360 stained HeLa cells. The cells were 4% PFA fixed (10 min) and then incubated in 1%BSA / 10% normal goat serum / 0.3M glycine in 0.1% PBS-Tween for 1h to permeabilise the cells and block non-specific protein-protein interactions. The cells were then incubated with the antibody (ab59360, 1µg/ml) overnight at +4°C. The secondary antibody (green) was Alexa Fluor® 488 goat anti-rabbit IgG (H+L) used at a 1/1000 dilution for 1h. Alexa Fluor® 594 WGA was used to label plasma membranes (red) at a 1/200 dilution for 1h. DAPI was used to stain the cell nuclei (blue) at a concentration of 1.43µM.
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