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Read our guarantee »Products:Cell Biology >> Apoptosis >> Intracellular >> Kinases
Anti-GAB1 antibody
See all GAB1 products (10) ...
Rabbit polyclonal to GAB1
Detects endogenous levels of total GAB1 protein.
WB, ELISA, IHC-Pmore details
Reacts with
Human
Predicted to work with
Mouse
Synthetic peptide: VEYLD, corresponding to amino acids 625-629 of Human GAB1 - around the phosphorylation site of Tyrosine 627.
VEYLD
Human umbilical vein endothelial cells.
Liquid
Store at -20°C. Stable for 12 months at -20°C
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
Affinity purified from rabbit antiserum by affinity chromatpgraphy using epitope specific immunogen.
Polyclonal
IgG
Cancer >> Signal transduction >> Other
Cancer >> Cell cycle >> Cell differentiation
Cell Biology >> Cell Cycle >> Cell differentiation
Signal Transduction >> Adapters >> Cytoplasmic
Signal Transduction >> Protein Phosphorylation >> Ser / Thr Kinases >> MAPK Pathway
Cell Biology >> Apoptosis >> Intracellular >> Kinases
Our Abpromise guarantee covers the use of ab47513 in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
WB: 1/500 - 1/1000.Detects a band of approximately 118 kDa (predicted molecular weight: 77 kDa).
ELISA: 1/20000
IHC-P: Use a concentration of 2 µg/mlPerform heat mediated antigen retrieval before commencing with IHC staining protocol.
Probably involved in EGF and insulin receptor signaling.
Belongs to the GAB family.
Contains 1 PH domain.
Phosphorylated on tyrosine residue(s) by the epidermal growth factor receptor (EGFR) and the insulin receptor (INSR). Tyrosine phosphorylation of GAB1 mediates interaction with several proteins that contain SH2 domains.
Target information above from: UniProt accessionQ13480
The UniProt Consortium
The Universal Protein Resource (UniProt) in 2010
Nucleic Acids Res. 38:D142-D148 (2010).
Western blot - GAB1 antibody (ab47513)

All lanes : Anti-GAB1 antibody (ab47513)
Lane 1 : HUVEC cell extract treated with EGF (200ng/ml, 10 min)
Lane 2 : HUVEC cell extract treated with EGF (200ng/ml, 10 min) with peptide
Lysates/proteins at 30 µg per lane.
Predicted band size : 77 kDa
Observed band size : 118 kDa (why is the actual band size different from the predicted?)
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)-GAB1 antibody(ab47513)

Ab47513 staining human normal tonsil. Staining is localised to the cytoplasm and cell membrane.
Left panel: with primary antibody at 2 ug/ml. Right panel: isotype control.
Sections were stained using an automated system DAKO Autostainer Plus , at room temperature. Sections were rehydrated and antigen retrieved with the Dako 3-in-1 antigen retrieval buffers EDTA pH 9.0 in a DAKO PT Link. Slides were peroxidase blocked in 3% H2O2 in methanol for 10 minutes. They were then blocked with Dako Protein block for 10 minutes (containing casein 0.25% in PBS) then incubated with primary antibody for 20 minutes and detected with Dako Envision Flex amplification kit for 30 minutes. Colorimetric detection was completed with diaminobenzidine for 5 minutes. Slides were counterstained with Haematoxylin and coverslipped under DePeX. Please note that for manual staining we recommend to optimize the primary antibody concentration and incubation time (overnight incubation), and amplification may be required.
ab47513 has not yet been referenced specifically in any publications.
Publishing research using ab47513? Please let us know so that we can cite the reference in this datasheet
Concentration of lot no. is
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All lanes : Anti-GAB1 antibody (ab47513)
Lane 1 : HUVEC cell extract treated with EGF (200ng/ml, 10 min)
Lane 2 : HUVEC cell extract treated with EGF (200ng/ml, 10 min) with peptide
Lysates/proteins at 30 µg per lane.
Predicted band size : 77 kDa
Observed band size : 118 kDa (why is the actual band size different from the predicted?)

Ab47513 staining human normal tonsil. Staining is localised to the cytoplasm and cell membrane.
Left panel: with primary antibody at 2 ug/ml. Right panel: isotype control.
Sections were stained using an automated system DAKO Autostainer Plus , at room temperature. Sections were rehydrated and antigen retrieved with the Dako 3-in-1 antigen retrieval buffers EDTA pH 9.0 in a DAKO PT Link. Slides were peroxidase blocked in 3% H2O2 in methanol for 10 minutes. They were then blocked with Dako Protein block for 10 minutes (containing casein 0.25% in PBS) then incubated with primary antibody for 20 minutes and detected with Dako Envision Flex amplification kit for 30 minutes. Colorimetric detection was completed with diaminobenzidine for 5 minutes. Slides were counterstained with Haematoxylin and coverslipped under DePeX. Please note that for manual staining we recommend to optimize the primary antibody concentration and incubation time (overnight incubation), and amplification may be required.
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