Anti-CD62E antibody [EPR28605-81]
- BOND RX™ Validated
- 20ul selling size
- Recombinant
- RabMAb
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Rabbit Recombinant Monoclonal CD62E antibody. Suitable for IHC-P, ICC/IF, WB and reacts with Transfected cell line - Human, Human, Mouse samples.
View Alternative Names
CD62E, ELAM1, SELE, E-selectin, CD62 antigen-like family member E, Endothelial leukocyte adhesion molecule 1, Leukocyte-endothelial cell adhesion molecule 2, ELAM-1, LECAM2
- ICC/IF
Supplier Data
Immunocytochemistry/ Immunofluorescence - Anti-CD62E antibody [EPR28605-81] (AB319105)
Immunofluorescent analysis of 4% Paraformaldehyde-fixed, 0.1% TritonX-100 permeabilized HUVEC (human umbilical vein endothelial cell) cells labelling CD62E with ab319105 at 1/50 (10.16 ug/ml) dilution, followed by ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed antibody at 1/1000 2 ug/ml dilution (Green).
Confocal image showing positive staining in HUVEC treated with IL-lbeta at 20ng/ml for 4 hours (shown in green). The counterstain was observed in magenta. Nuclear DNA was labelled with DAPI (shown in blue). Image was taken with a confocal microscope (Leica-Microsystems, TCS SP8).
ab195889 Anti-alpha Tubulin mouse monoclonal antibody - Microtubule Marker (Alexa Fluor® 594) was used to counterstain tubulin at 1/200 2.5ug/ml dilution (Magenta). The Nuclear counterstain was DAPI (Blue).
Secondary antibody only control : Secondary antibody is ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 2 ug/ml dilution.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-CD62E antibody [EPR28605-81] (AB319105)
Immunohistochemical analysis of paraffin-embedded Human colon carcinoma tissue labeling CD62E with ab319105 at 1/100 (5.08 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Positive staining on blood vessel of human colon carcinoma. The section was incubated with ab319105 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-CD62E antibody [EPR28605-81] (AB319105)
Immunohistochemical analysis of paraffin-embedded Human tonsil tissue labeling CD62E with ab319105 at 1/100 (5.08 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Positive staining on blood vessel of human tonsil. The section was incubated with ab319105 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-CD62E antibody [EPR28605-81] (AB319105)
Immunohistochemical analysis of paraffin-embedded (A) HEK-293T (human embryonic kidney epithelial cell) transfected with a human CD62E expression vector containing a Myc-His tag. (B) HEK-293T transfected with a human CD62L expression vector containing a Myc-His tag. (C) HEK-293T transfected with a human CD62P expression vector containing a Myc-His tag. (D) HEK-293T transfected with empty vector containing a Myc-His tag. tissue labeling CD62E with ab319105 at 1/2000 (0.254 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Positive staining on HEK-293T transfected with a Myc-His-tagged human CD62E construct (image A). No staining on HEK-293T transfected with a Myc-His-tagged human CD62L construct (image B), human CD62P construct (image C). No staining on HEK-293T transfected with empty plasmid (image D). The section was incubated with ab319105 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-CD62E antibody [EPR28605-81] (AB319105)
Immunohistochemical analysis of paraffin-embedded Human epityphlon tissue labeling CD62E with ab319105 at 1/100 (5.08 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Positive staining on blood vessel of human epityphlon. The section was incubated with ab319105 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-CD62E antibody [EPR28605-81] (AB319105)
Immunohistochemical analysis of paraffin-embedded Human liver tissue labeling CD62E with ab319105 at 1/100 (5.08 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Negative control : no staining on human liver. The section was incubated with ab319105 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-CD62E antibody [EPR28605-81] (AB319105)
Immunohistochemical analysis of paraffin-embedded Human cerebrum tissue labeling CD62E with ab319105 at 1/100 (5.08 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 ab319105 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-CD62E antibody [EPR28605-81] (AB319105)
Immunohistochemical analysis of paraffin-embedded Mouse cerebrum tissue labeling CD62E with ab319105 at 1/100 (5.08 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Negative control : no staining on mouse cerebrum. The section was incubated with ab319105 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-CD62E antibody [EPR28605-81] (AB319105)
Immunohistochemical analysis of paraffin-embedded Mouse liver tissue labeling CD62E with ab319105 at 1/100 (5.08 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Negative control : no staining on mouse liver. The section was incubated with ab319105 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-CD62E antibody [EPR28605-81] (AB319105)
Immunohistochemical analysis of paraffin-embedded Mouse crohn's disease model tissue labeling CD62E with ab319105 at 1/100 (5.08 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Positive staining on blood vessel of mouse crohn's disease model. The section was incubated with ab319105 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
Lab
Western blot - Anti-CD62E antibody [EPR28605-81] (AB319105)
Exposure time : Lane 1-2 : 180 seconds; Lane 3-4 : 7 seconds
In Western blot, Anti-GAPDH antibody [EPR16891] - Loading Control (ab181602) staining at 1/1000000 dilution.
ab319105 is more sensitive than ab300557 in WB testing.
Lanes 1 - 2:
Anti-CD62E antibody [EPR25616-62] (<a href='/en-us/products/primary-antibodies/cd62e-antibody-epr25616-62-ab300557'>ab300557</a>) at 1/1000 dilution
Lanes 3 - 4:
Western blot - Anti-CD62E antibody [EPR28605-81] (ab319105) at 1/1000 dilution
Lanes 1 and 3:
Untreated HUVEC (human umbilical vein endothelial cell) whole cell lysate at 20 µg
Lanes 2 and 4:
HUVEC treated with 20ng/ml IL-lbeta for 4h whole cell 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 1/20000 dilution
false
- WB
Lab
Western blot - Anti-CD62E antibody [EPR28605-81] (AB319105)
Blocking and diluting buffer and concentration : 5% NFDM/TBST.
Exposure Time Lane 1 : 180s, Lane 2 : 40s
Compared with ab300557, ab319105 and ab322206 have higher sensitivity, we recommend ab319105 and ab322206 as an alternative for testing CD62E in western blot.
Lanes 1 - 2:
Anti-CD62E antibody [EPR25616-62] (<a href='/en-us/products/primary-antibodies/cd62e-antibody-epr25616-62-ab300557'>ab300557</a>) at 1/1000 dilution
Lane 3:
Western blot - Anti-CD62E antibody [EPR28605-81] (ab319105) at 1/1000 dilution
Lane 4:
Western blot - Anti-CD62E antibody [RM2070] (<a href='/en-us/products/primary-antibodies/cd62e-antibody-rm2070-ab322206'>ab322206</a>) at 1/1000 dilution
All lanes:
HUVEC (human umbilical vein endothelial cell) treated with 20ng/ml IL- lbeta for 4h whole cell 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 1/20000 dilution
Observed band size: 100 kDa,115 kDa
false
- WB
Supplier Data
Western blot - Anti-CD62E antibody [EPR28605-81] (AB319105)
Blocking and diluting buffer and concentration : 5% NFDM/TBST.
The molecular weight observed is consistent with what has been described in the literature (PMID : 7589110).
In Western blot, Anti-GAPDH antibody [EPR16891] - Loading Control (ab181602) staining at 1/200000 dilution.
All lanes:
Western blot - Anti-CD62E antibody [EPR28605-81] (ab319105) at 1/1000 dilution
Lane 1:
Untreated HUVEC (human umbilical vein endothelial cell) whole cell lysate at 30 µg
Lane 2:
HUVEC treated with 20ng/ml IL-lbeta for 4h whole cell lysate at 30 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 1/20000 dilution
Observed band size: 100 kDa,115 kDa,36 kDa
false
Exposure time: 125s
- WB
Supplier Data
Western blot - Anti-CD62E antibody [EPR28605-81] (AB319105)
Blocking and diluting buffer and concentration : 5% NFDM/TBST.
The molecular weight observed is consistent with what has been described in the literature (PMID : 7589110).
Negative control : Neuro-2a.
In Western blot, Anti-GAPDH antibody [EPR16891] - Loading Control (ab181602) staining at 1/200000 dilution.
All lanes:
Western blot - Anti-CD62E antibody [EPR28605-81] (ab319105) at 1/1000 dilution
Lane 1:
CT26.WT (mouse colorectal carcinoma fibroblast) whole cell lysate at 20 µg
Lane 2:
Neuro-2a (mouse neuroblastoma neuroblast) whole cell 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 1/20000 dilution
Observed band size: 100 kDa,115 kDa,36 kDa
false
Exposure time: 59s
Related conjugates and formulations (1)
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Anti-CD62E antibody [EPR28605-81] - BSA and Azide free
Reactivity data
Product details
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.
Properties and storage information
Form
Purification technique
Storage buffer
Shipped at conditions
Appropriate short-term storage duration
Appropriate short-term storage conditions
Appropriate long-term storage conditions
Aliquoting information
Storage information
Supplementary information
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
E-selectin facilitates leukocyte adhesion by binding specific carbohydrate ligands on the surface of circulating immune cells. This binding is critical in the cascade of events that leads to leukocyte extravasation into tissues. E-selectin does not work in isolation rather forming part of a complex interaction with other cell adhesion molecules such as P-selectin and L-selectin. These interactions ensure precise control of cellular traffic during inflammatory responses.
Pathways
CD62E engages in the inflammatory signaling pathways including the NF-kB pathway. This pathway modulates the expression of E-selectin in response to pro-inflammatory cytokines like interleukin-1 and tumor necrosis factor-alpha. CD62E interacts with integrins on leukocytes and has downstream effects on cellular processes involved in immune response. Its cooperation with proteins like ICAM-1 and VCAM-1 further integrates it into a network of adhesion molecules maintaining vascular stability and immune surveillance.
Product protocols
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Target data
Product promise
Please note: All products are 'FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC OR THERAPEUTIC PROCEDURES'.
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