Anti-Fc epsilon RI/FCER1A antibody [EPR28402-78] - BSA and Azide free
- BOND RX™ Validated
- Recombinant
- Advanced Validation
- RabMAb
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Rabbit Recombinant Monoclonal Fc epsilon RI/FCER1A antibody. Carrier free. Suitable for mIHC, WB, IHC-P and reacts with Human samples.
View Alternative Names
FCE1A, FCER1A, High affinity immunoglobulin epsilon receptor subunit alpha, Fc-epsilon RI-alpha, IgE Fc receptor subunit alpha, FcERI
- mIHC
Lab
Multiplex immunohistochemistry - Anti-Fc epsilon RI/FCER1A antibody [EPR28402-78] - BSA and Azide free (AB316200)
This data was developed using ab316199, the same antibody clone in a different buffer formulation.
Multiplex immunohistochemistry analysis of formalin/PFA-fixed paraffin-embedded Human stomach cancer tissue staining Fc epsilon RI/FCER1A with ab316199 at a 1 : 500 (1.04 ug/ml) dilution and SIGLEC6 with ab317307 at 1 : 100 (4.89 ug/ml) dilution followed by secondary antibody Opal Polymer HRP Ms + Rb.
Panel A : merged staining of anti-Fc epsilon RI/FCER1A (green; Opal™520) and anti-SIGLEC6 (magenta; Opal™690) on human stomach cancer. Panel B : anti-Fc epsilon RI/FCER1A staining immune cells in human stomach cancer.Panel C : anti-SIGLEC6 staining mast cells and basophils in human stomach cancer. Panel D : Nuclear DNA was labeled with DAPI (shown in blue).
The section was incubated in two rounds of staining : in the order of ab316199 and ab317307 for 30 mins at room temperature. Each round was followed by a separate fluorescent tyramide signal amplification system.
The immunostaining was performed on a Leica Biosystems BOND® RX instrument with an Opal™ 4-color kit. Image acquisition was performed with Leica SP8 confocal microscope.
Heat mediated antigen retrieval was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Fc epsilon RI/FCER1A antibody [EPR28402-78] - BSA and Azide free (AB316200)
This data was developed using ab316199, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded (A) KU812(human peripheral blood basophils) cell pellet . (B) HEK-293T (human embryonic kidney epithelial cell) cell pellet . tissue labeling Fc epsilon RI/FCER1A with ab316199 at 1/500 (1.04 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Positive staining on (A) KU812 cell pellet . No staining on (B) HEK-293T cell pellet.
The section was incubated with ab316199 for 30 mins at room temperature.
The immunostaining was performed on a Leica Biosystems BOND® RX instrument.
Counterstained with Hematoxylin.
Secondary antibody only control : Secondary antibody is a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Heat mediated antigen retrieval was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Fc epsilon RI/FCER1A antibody [EPR28402-78] - BSA and Azide free (AB316200)
This data was developed using ab316199, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Human squamous cell lung carcinoma tissue labeling Fc epsilon RI/FCER1A with ab316199 at 1/500 (1.04 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Positive staining on immune cells of human lung carcinoma.
The section was incubated with ab316199 for 30 mins at room temperature.
The immunostaining was performed on a Leica Biosystems BOND® RX instrument.
Counterstained with Hematoxylin.
Secondary antibody only control : Secondary antibody is a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Heat mediated antigen retrieval was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins.
- mIHC
Lab
Multiplex immunohistochemistry - Anti-Fc epsilon RI/FCER1A antibody [EPR28402-78] - BSA and Azide free (AB316200)
This data was developed using ab316199, the same antibody clone in a different buffer formulation.
Multiplex immunohistochemistry analysis of formalin/PFA-fixed paraffin-embedded Human lung tissue staining Fc epsilon RI/FCER1A with ab316199 at a 1 : 500 (1.04 ug/ml) dilution and SIGLEC6 with ab317307 at 1 : 100 (4.89 ug/ml) dilution followed by secondary antibody Opal Polymer HRP Ms + Rb.
Panel A : merged staining of anti-Fc epsilon RI/FCER1A (green; Opal™520) and anti-SIGLEC6 (magenta; Opal™690) on human lung. Panel B : anti-Fc epsilon RI/FCER1A staining immune cells in human lung.Panel C : anti-SIGLEC6 staining mast cells and basophils in human lung. Panel D : Nuclear DNA was labeled with DAPI (shown in blue).
The section was incubated in two rounds of staining : in the order of ab316199 and ab317307 for 30 mins at room temperature. Each round was followed by a separate fluorescent tyramide signal amplification system.
The immunostaining was performed on a Leica Biosystems BOND® RX instrument with an Opal™ 4-color kit. Image acquisition was performed with Leica SP8 confocal microscope.
Heat mediated antigen retrieval was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Fc epsilon RI/FCER1A antibody [EPR28402-78] - BSA and Azide free (AB316200)
This data was developed using ab316199, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Human cerebrum tissue labeling Fc epsilon RI/FCER1A with ab316199 at 1/500 (1.04 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Negative control : no staining on human cerebrum.
The section was incubated with ab316199 for 30 mins at room temperature.
The immunostaining was performed on a Leica Biosystems BOND® RX instrument.
Counterstained with Hematoxylin.
Secondary antibody only control : Secondary antibody is a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Heat mediated antigen retrieval was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Fc epsilon RI/FCER1A antibody [EPR28402-78] - BSA and Azide free (AB316200)
This data was developed using ab316199, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Human tonsil tissue labeling Fc epsilon RI/FCER1A with ab316199 at 1/500 (1.04 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Positive staining on human tonsil.
The section was incubated with ab316199 for 30 mins at room temperature.
The immunostaining was performed on a Leica Biosystems BOND® RX instrument.
Counterstained with Hematoxylin.
Secondary antibody only control : Secondary antibody is a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Heat mediated antigen retrieval was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Fc epsilon RI/FCER1A antibody [EPR28402-78] - BSA and Azide free (AB316200)
This data was developed using ab316199, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Human lung tissue labeling Fc epsilon RI/FCER1A with ab316199 at 1/500 (1.04 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Positive staining on immune cells of human lung (PMID : 21958156).
The section was incubated with ab316199 for 30 mins at room temperature.
The immunostaining was performed on a Leica Biosystems BOND® RX instrument.
Counterstained with Hematoxylin.
Secondary antibody only control : Secondary antibody is a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Heat mediated antigen retrieval was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins.
- WB
Supplier Data
Western blot - Anti-Fc epsilon RI/FCER1A antibody [EPR28402-78] - BSA and Azide free (AB316200)
This data was developed using ab316199, the same antibody clone in a different buffer formulation.
Fc epsilon RI/FCER1A is a glycoprotein of approximately 45 kDa and detected as a 30-kDa band after treated with Peptide : N-glycosidase F (PNGase F).
The expression profile/ molecular weight observed is consistent with what has been described in the literature (PMID : 2964640).
Samples are non-boiled as boiling may cause protein aggregation.
In Western blot, Anti-GAPDH antibody [EPR16891] - Loading Control (ab181602) staining at 1/200000 dilution.
All lanes:
Western blot - Anti-Fc epsilon RI/FCER1A antibody [EPR28402-78] (<a href='/en-us/products/primary-antibodies/fc-epsilon-ri-fcer1a-antibody-epr28402-78-ab316199'>ab316199</a>) at 1/1000 dilution
Lane 1:
Untreated KU812 (human Peripheral blood basophil) whole cell lysate at 40 µg
Lane 2:
KU812 treated with Peptide:N-glycosidase F (PNGase F) whole cell lysate at 40 µg
Secondary
All lanes:
Western blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/en-us/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/100000 dilution
Observed band size: 30 kDa,45 kDa,36 kDa
true
Exposure time: 81s
- WB
Supplier Data
Western blot - Anti-Fc epsilon RI/FCER1A antibody [EPR28402-78] - BSA and Azide free (AB316200)
This data was developed using ab316199, the same antibody clone in a different buffer formulation.
Negative control : HEK-293 (PMID : 17728245).
Samples are non-boiled as boiling may cause protein aggregation.
In Western blot, Anti-Vinculin antibody [EPR8185] (ab129002) staining at 1/10000 dilution.
All lanes:
Western blot - Anti-Fc epsilon RI/FCER1A antibody [EPR28402-78] (<a href='/en-us/products/primary-antibodies/fc-epsilon-ri-fcer1a-antibody-epr28402-78-ab316199'>ab316199</a>) at 1/1000 dilution
Lane 1:
KU812 (human Peripheral blood basophil) whole cell lysate at 40 µg
Lane 2:
HEK-293 (human embryonic kidney epithelial cell) whole cell lysate at 40 µg
Secondary
All lanes:
Western blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/en-us/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/100000 dilution
Observed band size: 45 kDa,124 kDa
false
Exposure time: 180s
- WB
Supplier Data
Western blot - Anti-Fc epsilon RI/FCER1A antibody [EPR28402-78] - BSA and Azide free (AB316200)
This data was developed using ab316199, the same antibody clone in a different buffer formulation.
Negative control : brain (PMID : 2964640).
The expression profile/ molecular weight observed is consistent with what has been described in the literature (PMID : 2964640).
Samples are non-boiled as boiling may cause protein aggregation.
In Western blot, Anti-GAPDH antibody [EPR16891] - Loading Control (ab181602) staining at 1/200000 dilution.
All lanes:
Western blot - Anti-Fc epsilon RI/FCER1A antibody [EPR28402-78] (<a href='/en-us/products/primary-antibodies/fc-epsilon-ri-fcer1a-antibody-epr28402-78-ab316199'>ab316199</a>) at 1/1000 dilution
Lane 1:
Human tonsil tissue lysate at 40 µg
Lane 2:
Human brain tissue lysate at 40 µg
Lane 3:
Human testis tissue lysate at 40 µg
Lane 4:
Human bone marrow tissue lysate at 40 µg
Lane 5:
Human skin tissue lysate at 20 µg
Secondary
All lanes:
Western blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/en-us/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/100000 dilution
Observed band size: 55-60 kDa,36 kDa
false
Exposure time: 180s
Related conjugates and formulations (1)
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Anti-Fc epsilon RI/FCER1A antibody [EPR28402-78]
Reactivity data
Product details
ab316200 is the carrirer-free version of ab316199.
Patented technology
Our RabMAb® technology is a patented hybridoma-based technology for making rabbit monoclonal antibodies. For details on our patents, please refer to RabMAb® patents.
What are the advantages of a recombinant monoclonal antibody?
This product is a recombinant monoclonal antibody, which offers several advantages including:
- - High batch-to-batch consistency and reproducibility
- - Improved sensitivity and specificity
- - Long-term security of supply
- - Animal-free batch production
For more information, read more on recombinant antibodies.
Conjugation ready
Our carrier-free antibodies are typically supplied in a PBS-only formulation, purified and free of BSA, sodium azide and glycerol. This conjugation-ready format is designed for use with fluorochromes, metal isotopes, oligonucleotides, and enzymes, which makes them ideal for antibody labelling, functional and cell-based assays, flow-based assays (e.g. mass cytometry) and Multiplex Imaging applications.
Use our conjugation kits for antibody conjugates that are ready-to-use in as little as 20 minutes with 1 minute hands-on-time and 100% antibody recovery: available for fluorescent dyes, HRP, biotin and gold.
Compatibility
This product is compatible with the Maxpar® Antibody Labeling Kit from Fluidigm, without the need for antibody preparation. Maxpar® is a trademark of Fluidigm Canada Inc.
Properties and storage information
Form
Purification technique
Storage buffer
Shipped at conditions
Appropriate short-term storage conditions
Appropriate long-term storage conditions
Product protocols
- Visit the General protocols
- Visit the Troubleshooting
Target data
Product promise
Please note: All products are 'FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC OR THERAPEUTIC PROCEDURES'.
For licensing inquiries, please contact partnerships@abcam.com