Anti-Apolipoprotein E antibody [EP1374Y] - BSA and Azide free
- BOND RX™ Validated
- RabMAb
- Recombinant
- KO Validated
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Knockout Tested Rabbit Recombinant Monoclonal Apolipoprotein E antibody. Carrier free. Suitable for ICC/IF, IP, WB, IHC-P, Flow Cyt (Intra) and reacts with Human samples.
View Alternative Names
Apolipoprotein E, Apo-E, APOE
- IHC-P
Lab
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Apolipoprotein E antibody [EP1374Y] - BSA and Azide free (AB271843)
This data was developed using ab52607, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded human basal ganglia tissue* labelling APOE with ab52607 at 0.1ug/ml followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Positive staining in human basal ganglia.
The section was incubated with ab52607 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 with sodium citrate buffer (pH 6.0 epitope retrieval solution1) for 20 mins.
*Tissue obtained from the Human Research Tissue Bank, supported by the NIHR Cambridge Biomedical Research Centre.
- IHC-P
Lab
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Apolipoprotein E antibody [EP1374Y] - BSA and Azide free (AB271843)
This data was developed using ab52607, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded human Alzheimer's brain tissue* labelling APOE with ab52607 at 0.1ug/ml followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Positive staining in human Alzheimer's brain.
The section was incubated with ab52607 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 with sodium citrate buffer (pH 6.0 epitope retrieval solution1) for 20 mins.
*Tissue obtained from the Human Research Tissue Bank, supported by the NIHR Cambridge Biomedical Research Centre.
- Flow Cyt (Intra)
Unknown
Flow Cytometry (Intracellular) - Anti-Apolipoprotein E antibody [EP1374Y] - BSA and Azide free (AB271843)
Intracellular Flow Cytometry analysis of HepG2 (Human hepatocellular carcinoma epithelial cell) cells labeling Apolipoprotein E (red) with purified ab52607 at a 1/250 dilution (10ug/mL). Cells were fixed with 4% paraformaldehyde and permeabilized with 90% methanol. A goat anti rabbit IgG (Alexa Fluor®488) (ab150077) was used as the secondary antibody at a 1/2000 dilution. Black - Rabbit monoclonal IgG (Black) (ab172730). Blue (unlabeled control) - Cell without incubation with primary antibody and secondary antibody (Blue).
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab52607).
- IHC-P
Lab
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Apolipoprotein E antibody [EP1374Y] - BSA and Azide free (AB271843)
This data was developed using ab52607, the same antibody clone in a different buffer formulation.
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) analysis of Human astrocytoma tissue sections labeling Apolipoprotein E with purified ab52607 at 1/800 dilution (0.13 µg/mL). Heat mediated antigen retrieval using Bond™ Epitope Retrieval Solution 2 (pH 9.0). The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Rabbit specific IHC polymer detection kit HRP/DAB (ab209101) was used as the secondary antibody. Negative control : PBS instead of the primary antibody. Hematoxylin was used as a counterstain.
- ICC/IF
Lab
Immunocytochemistry/ Immunofluorescence - Anti-Apolipoprotein E antibody [EP1374Y] - BSA and Azide free (AB271843)
This data was developed using ab52607, the same antibody clone in a different buffer formulation.
Immunocytochemistry analysis of HepG2 (Human hepatocellular carcinoma epithelial cell) cells labeling Apolipoprotein E with Purified ab52607 at 1 : 50 dilution (2.0 μg/ml). Cells were fixed in 4% Paraformaldehyde and permeabilized with 0.1% tritonX-100. Cells were counterstained with ab195889 Anti-alpha Tubulin antibody [DM1A] - Microtubule Marker (Alexa Fluor® 594) 1 : 200 (2.5 μg/ml). Goat anti rabbit IgG (Alexa Fluor® 488,ab150077) was used as the secondary antibody at 1 : 1000 (2 μg/ml) dilution. DAPI (blue) was used as nuclear counterstain. PBS instead of the primary antibody was used as the secondary antibody only control.
- IP
Unknown
Immunoprecipitation - Anti-Apolipoprotein E antibody [EP1374Y] - BSA and Azide free (AB271843)
This data was developed using ab52607, the same antibody clone in a different buffer formulation.
Purified ab52607 at 1/20 dilution (0.5μg) immunoprecipitating Apolipoprotein E in HepG2 whole cell lysate.
Lane 1 (input) : HepG2 (Human hepatocellular carcinoma epithelial cell) whole cell lysate 10μg
Lane 2 (+) : ab52607 + HepG2 whole cell lysate.
Lane 3 (-) : Rabbit monoclonal IgG (ab172730) instead of ab52607 in HepG2 whole cell lysate.
VeriBlot for IP Detection Reagent (HRP) (ab131366) (1/5000 dilution) was used for Western blotting.
Blocking Buffer and concentration : 5% NFDM/TBST.
Diluting buffer and concentration : 5% NFDM/TBST.
Observed band size : 36 kDa
All lanes:
Immunoprecipitation - Anti-Apolipoprotein E antibody [EP1374Y] - BSA and Azide free (ab271843)
Predicted band size: 36 kDa
false
- IP
Lab
Immunoprecipitation - Anti-Apolipoprotein E antibody [EP1374Y] - BSA and Azide free (AB271843)
Immunoprecipitation of APOE in HAP1 cells. Lysates were prepared and immunoprecipitation was performed using 2.0 µg of ab52607 pre-coupled to Protein A beads. Samples were then washed and processed for western blot
These data were provided by YCharOS Inc., an open science company with the mission of characterizing commercially available antibody reagents for all human proteins. Abcam and YCharOS are working together to help address the reproducibility crisis by enabling the life science community to better evaluate commercially available antibodies.
All lanes:
Immunoprecipitation - Anti-Apolipoprotein E antibody [EP1374Y] (<a href='/en-us/products/primary-antibodies/apolipoprotein-e-antibody-ep1374y-ab52607'>ab52607</a>) at 2 µg
All lanes:
HAP1 cells
false
- WB
Unknown
Western blot - Anti-Apolipoprotein E antibody [EP1374Y] - BSA and Azide free (AB271843)
This data was developed using ab52607, the same antibody clone in a different buffer formulation.
All lanes:
Western blot - Anti-Apolipoprotein E antibody [EP1374Y] (<a href='/en-us/products/primary-antibodies/apolipoprotein-e-antibody-ep1374y-ab52607'>ab52607</a>) at 1/10000 dilution
Lane 1:
Human liver lysate at 20 µg
Lane 2:
Human cerebellum lysate at 20 µg
Lane 3:
HepG2 (Human hepatocellular carcinoma epithelial cell) whole cell lysate at 20 µg
Lane 4:
Human serum lysate at 15 µg
Secondary
All lanes:
Goat Anti-Rabbit IgG (HRP) with minimal cross-reactivity with human IgG at 1/2000 dilution
Predicted band size: 36 kDa
false
- WB
Lab
Western blot - Anti-Apolipoprotein E antibody [EP1374Y] - BSA and Azide free (AB271843)
ab52607 was shown to react with APOE in wild-type HAP1 cells in Western blot with loss of signal observed in a APOE knockout cell line. Wild-type HAP1 and APOE knockout cell lysates were subjected to SDS-PAGE. Membranes were blocked in 5% milk in TBST for 1 hr before incubation with ab52607 overnight at 4 °C at a 1/1000 dilution. Blots were incubated with secondary antibodies at 0.2ug/mL before imaging.
These data were provided by YCharOS Inc., an open science company with the mission of characterizing commercially available antibody reagents for all human proteins. Abcam and YCharOS are working together to help address the reproducibility crisis by enabling the life science community to better evaluate commercially available antibodies.
All lanes:
Western blot - Anti-Apolipoprotein E antibody [EP1374Y] (<a href='/en-us/products/primary-antibodies/apolipoprotein-e-antibody-ep1374y-ab52607'>ab52607</a>) at 1/1000 dilution
Lane 1:
Wild-type HAP1 lysate at 20 µg
Lane 2:
APOE Knockout HAP1 lysate at 20 µg
Observed band size: 36 kDa
false
- WB
Lab
Western blot - Anti-Apolipoprotein E antibody [EP1374Y] - BSA and Azide free (AB271843)
False colour image of Western blot : Anti-Apolipoprotein E antibody [EP1374Y] staining at 1/1000 dilution, shown in green; Mouse anti-Alpha Tubulin [DM1A] (ab7291) loading control staining at 1/20000 dilution, shown in red. In Western blot, ab52607 was shown to bind specifically to Apolipoprotein E. A band was observed at 34-37 kDa in wild-type HepG2 cell lysates with no signal observed at this size in APOE knockout cell line. To generate this image, wild-type and APOE knockout HepG2 cell lysates were analysed. First, samples were run on an SDS-PAGE gel then transferred onto a nitrocellulose membrane. Membranes were blocked in 5 % milk in TBS-0.1 % Tween® 20 (TBS-T) before incubation with primary antibodies overnight at 4 °C. Blots were washed four times in TBS-T, incubated with secondary antibodies for 1 h at room temperature, washed again four times then imaged. Secondary antibodies used were Goat anti-Rabbit IgG H&L (IRDye® 800CW) preabsorbed (ab216773) and Goat anti-Mouse IgG H&L (IRDye® 680RD) preabsorbed (ab216776) at 1/20000 dilution.
All lanes:
Western blot - Anti-Apolipoprotein E antibody [EP1374Y] (<a href='/en-us/products/primary-antibodies/apolipoprotein-e-antibody-ep1374y-ab52607'>ab52607</a>) at 1/1000 dilution
Lane 1:
Wild-type HepG2 cell lysate at 20 µg
Lane 2:
APOE knockout HepG2 cell lysate at 20 µg
Lane 2:
Western blot - Human APOE knockout Hep G2 cell line (<a href='/en-us/products/cell-lines/human-apoe-knockout-hep-g2-cell-line-ab280875'>ab280875</a>)
Lane 3:
Human Liver cell lysate at 20 µg
Lane 4:
Human Kidney cell lysate at 20 µg
Predicted band size: 36 kDa
Observed band size: 34 kDa,34-37 kDa
false
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Alexa Fluor® 647 Anti-Apolipoprotein E antibody [EP1374Y]
Reactivity data
Product details
ab271843 is the carrier-free version of ab52607.
Species reactivity
Mouse, Rat: We have preliminary internal testing data to indicate this antibody may not react with these species.
Please contact us for more information.
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
Storage information
Supplementary information
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
ApoE mediates the binding internalization and catabolism of these lipoprotein particles facilitating their interaction with specific cell-surface receptors such as the LDL receptor. This protein operates as part of a complex that includes various other apolipoproteins and lipid molecules. The study of mouse apoe using tools like a mouse apoe ELISA provides valuable data due to its similar physiological functions in lipid transport and metabolism.
Pathways
In the lipid metabolism pathway ApoE interacts with proteins such as the LDL receptor influencing the clearance of chylomicron remnants and VLDL from the bloodstream. In the cardiovascular disease pathway this protein impacts cholesterol levels and promotes plaques stabilization. ApoE's role in these pathways offers insights into its interaction with related proteins like apolipoprotein B and LDL receptor which are critical for maintaining lipid equilibrium.
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'.
For licensing inquiries, please contact partnerships@abcam.com