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Read our guarantee »Products:Tags & Cell Markers >> Cell Type Markers >> Tumor Associated
Anti-ErbB 4 antibody [HFR1]
See all ErbB 4 products (14) ...
Mouse monoclonal [HFR1] to ErbB 4
Flow Cyt, ICC/IF, WB, IP, IHC-Pmore details
Reacts with
Mouse, Human
Predicted to work with
Rat, Chicken
Synthetic peptide: (C)RSTLQHPDYLQEYST , corresponding to amino acids 1250-1264 of HER4.
(C)RSTLQHP DYLQEYST
Human A431 cell and mouse NIH3T3/HER4 cell extracts (western blot). NIH3T3 cells (IHC-P).
Liquid
Shipped at 4°C. Upon delivery aliquot and store at -20°C. Avoid freeze / thaw cycles.
Preservative: 0.05% Sodium Azide
Constituents: PBS, 1mg/ml BSA
Concentration information loading...
Protein A purified
Monoclonal
HFR1
IgG2b
Cancer >> Tumor biomarkers >> Oncoproteins
Cancer >> Oncoproteins/suppressors >> Oncoproteins >> Growth factors
Cancer >> Growth factors >> EGF
Signal Transduction >> Growth Factors/Hormones >> EGF
Signal Transduction >> Protein Phosphorylation >> Tyrosine Kinases >> Receptor Tyrosine Kinases
Tags & Cell Markers >> Cell Type Markers >> Tumor Associated
Our Abpromise guarantee covers the use of ab19391 in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
Flow Cyt: Use 2µg for 106 cells.
ICC/IF: Use a concentration of 1 - 5 µg/ml.
WB: Use a concentration of 3 µg/mlDetects a band of approximately 185 kDa (predicted molecular weight: 147 kDa).
IP: Use at an assay dependent dilution.
IHC-P: Use a concentration of 6 - 8 µg/ml.
Specifically binds and is activated by neuregulins, NRG-2, NRG-3, heparin-binding EGF-like growth factor, betacellulin and NTAK. Interaction with these factors induces cell differentiation. Not activated by EGF, TGF-A, and amphiregulin. The C-terminal fragment (CTF) of isoform JMA-A CYT-2 (containing E4ICD2) can stimulate transcription in the presence of YAP1. ERBB4 intracellular domain is involved in the regulation of cell growth. Conflicting reports are likely due at least in part to the opposing effects of the isoform-specific and nuclear-translocated ERBB4 intracellular domains (E4ICD1 and E4ICD2). Overexpression studies in epithelium show growth inhibition using E4ICD1 and increased proliferation using E4ICD2. E4ICD2 has greater in vitro kinase activity than E4ICD1. The kinase activity is required for the nuclear translocation of E4ICD2.
Expressed at highest levels in brain, heart, kidney, in addition to skeletal muscle, parathyroid, cerebellum, pituitary, spleen, testis and breast. Lower levels in thymus, lung, salivary gland, and pancreas. Isoform JM-A CYT-1 and isoform JM-B CYT-1 are expressed in cerebellum, but only the isoform JM-B is expressed in the heart.
Belongs to the protein kinase superfamily. Tyr protein kinase family. EGF receptor subfamily.
Contains 1 protein kinase domain.
Isoform JM-A CYT-1 and isoform JM-A CYT-2 but not isoform JM-B CYT-1 and isoform JM-B CYT-2 are processed by ADAM17. Proteolytic processing in response to ligand or 12-O-tetradecanoylphorbol-13-acetate stimulation results in the production of 120 kDa soluble receptor forms and intermediate membrane-anchored 80 kDa fragments (m80HER4), which are further processed by a presenilin-dependent gamma-secretase to release the respective cytoplasmic intracellular domain E4ICD (either E4ICD1/s80Cyt1 or E4ICD2/s80Cyt2). Membrane-anchored 80 kDa fragments of the processed isoform JM-A CYT-1 are more readily degraded by the proteasome than fragments of isoform JM-A CYT-2 suggesting a prevalence of E4ICD2 over E4ICD1.
Ligand-binding increases phosphorylation on tyrosine residues. Isoform JM-A CYT-2 is constitutively phosphorylated on tyrosine residues in a ligand-independent manner. E4ICD2 but not E4ICD1 is phosphorylated on tyrosine residues.
Ubiquitinated. The ERBB4 intracellular domain is ubiquitinated and targeted to proteosomal degradation during mitosis mediated by the APC/C complex. Isoform JM-A CYT-1 and isoform JM-B CYT-1 are ubiquitinated by WWP1. The ERBB4 intracellular domain (E4ICD1) is ubiquitinated, and this involves NEDD4.
Membrane and Nucleus. Following proteolytical processing E4ICD (E4ICD1 or E4ICD2 generated from the respective isoforms) is translocated to the nucleus. Significantly more E4ICD2 than E4ICD1 is found in the nucleus. E4ICD2 colocalizes with YAP1 in the nucleus.
Target information above from: UniProt accessionQ15303
The UniProt Consortium
The Universal Protein Resource (UniProt) in 2010
Nucleic Acids Res. 38:D142-D148 (2010).
Immunocytochemistry/ Immunofluorescence - ErbB 4 antibody [HFR1] (ab19391)
![Immunocytochemistry/ Immunofluorescence - ErbB 4 antibody [HFR1] (ab19391)](/ps/datasheet/images/19/ab19391/ErbB-4-Primary-antibodies-ab19391-1.jpg)
ICC/IF image of ab19391 stained HepG2 cells. The cells were 4% formaldehyde 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 (ab19391, 1µg/ml) overnight at +4°C. The secondary antibody (green) was Alexa Fluor® 488 goat anti-mouse 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.
Flow Cytometry - ErbB 4 antibody [HFR1] (ab19391)
![Flow Cytometry - ErbB 4 antibody [HFR1] (ab19391)](/ps/datasheet/images/19/ab19391/ErbB-4-Primary-antibodies-ab19391-2.jpg)
Overlay histogram showing HEK293 cells stained with ab19391 (red line). The cells were fixed with methanol (5 min) and then permeabilized with 0.1% PBS-Tween for 20 min. The cells were then incubated in 1x PBS / 10% normal goat serum / 0.3M glycine to block non-specific protein-protein interactions followed by the antibody (ab19391, 2µg/1x106 cells) for 30 min at 22°C. The secondary antibody used was DyLight® 488 goat anti-mouse IgG (H+L) (ab96879) at 1/500 dilution for 30 min at 22°C. Isotype control antibody (black line) was mouse IgG2b [PLPV219] (ab91366, 2µg/1x106 cells) used under the same conditions. Acquisition of >5,000 events was performed. This antibody gave a positive signal in HEK293 cells fixed with 4% paraformaldehyde (10 min)/permeabilized in 0.1% PBS-Tween used under the same conditions.
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - ErbB 4 antibody [HFR1] (ab19391)
![Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - ErbB 4 antibody [HFR1] (ab19391)](/ps/datasheet/images/19/ab19391/ErbB-4-Primary-antibodies-ab19391-7.jpg)
ab19391 staining ErbB 4 in Mouse brain tissue by Immunohistochemistry (Frozen sections). The sections were fixed with paraformaldehyde. The primary antibody was used neat and incubated with the sample for 12 hours at 4°C. A Biotin-conjugated Rabbit anti-Mouse polyclonal was used as the secondary antibody.
This image is courtesy of an Anonymous Abreview.
This product has been referenced in:
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![Immunocytochemistry/ Immunofluorescence - ErbB 4 antibody [HFR1] (ab19391)](/ps/datasheet/images/19/ab19391/ErbB-4-Primary-antibodies-ab19391-1.jpg)
ICC/IF image of ab19391 stained HepG2 cells. The cells were 4% formaldehyde 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 (ab19391, 1µg/ml) overnight at +4°C. The secondary antibody (green) was Alexa Fluor® 488 goat anti-mouse 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.
![Flow Cytometry - ErbB 4 antibody [HFR1] (ab19391)](/ps/datasheet/images/19/ab19391/ErbB-4-Primary-antibodies-ab19391-2.jpg)
Overlay histogram showing HEK293 cells stained with ab19391 (red line). The cells were fixed with methanol (5 min) and then permeabilized with 0.1% PBS-Tween for 20 min. The cells were then incubated in 1x PBS / 10% normal goat serum / 0.3M glycine to block non-specific protein-protein interactions followed by the antibody (ab19391, 2µg/1x106 cells) for 30 min at 22°C. The secondary antibody used was DyLight® 488 goat anti-mouse IgG (H+L) (
![Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - ErbB 4 antibody [HFR1] (ab19391)](/ps/datasheet/images/19/ab19391/ErbB-4-Primary-antibodies-ab19391-7.jpg)
ab19391 staining ErbB 4 in Mouse brain tissue by Immunohistochemistry (Frozen sections). The sections were fixed with paraformaldehyde. The primary antibody was used neat and incubated with the sample for 12 hours at 4°C. A Biotin-conjugated Rabbit anti-Mouse polyclonal was used as the secondary antibody.
This image is courtesy of an Anonymous Abreview.
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