Anti-CD46 antibody [EPR4014] (ab108307) is a rabbit monoclonal antibody that is used to detect CD46 in Western Blot, IHC-P. Suitable for Human samples.
- Specificity confirmed with CD46 knockout cell line validation
pH: 7.2 - 7.4
Preservative: 0.01% Sodium azide
Constituents: 59% PBS, 40% Glycerol (glycerin, glycerine), 0.05% BSA
IHC-P | IP | Flow Cyt | WB | |
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Human | Tested | Not recommended | Not recommended | Tested |
Rabbit | Predicted | Not recommended | Not recommended | Predicted |
Species | Dilution info | Notes |
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Species Human | Dilution info 1/500 - 1/1000 | Notes Perform heat-mediated antigen retrieval via the pressure cooker method before commencing with IHC staining protocol. |
Species | Dilution info | Notes |
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Species Rabbit | Dilution info - | Notes - |
Species | Dilution info | Notes |
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Species Human, Rabbit | Dilution info - | Notes - |
Species | Dilution info | Notes |
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Species Human, Rabbit | Dilution info - | Notes - |
Species | Dilution info | Notes |
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Species Human | Dilution info 1/1000 - 1/10000 | Notes - |
Species | Dilution info | Notes |
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Species Rabbit | Dilution info - | Notes - |
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Acts as a cofactor for complement factor I, a serine protease which protects autologous cells against complement-mediated injury by cleaving C3b and C4b deposited on host tissue. May be involved in the fusion of the spermatozoa with the oocyte during fertilization. Also acts as a costimulatory factor for T-cells which induces the differentiation of CD4+ into T-regulatory 1 cells. T-regulatory 1 cells suppress immune responses by secreting interleukin-10, and therefore are thought to prevent autoimmunity. (Microbial infection) A number of viral and bacterial pathogens seem to bind MCP in order to exploit its immune regulation property and directly induce an immunosuppressive phenotype in T-cells. (Microbial infection) Acts as a receptor for Adenovirus subgroup B2 and Ad3. (Microbial infection) Acts as a receptor for cultured Measles virus. (Microbial infection) Acts as a receptor for Herpesvirus 6/HHV-6. (Microbial infection) May act as a receptor for pathogenic bacteria Neisseria and Streptococcus pyogenes (PubMed:11260136, PubMed:11971006, PubMed:7708671, PubMed:9379894).
CD46, MCP, MIC10, Membrane cofactor protein, TLX, Trophoblast leukocyte common antigen
Anti-CD46 antibody [EPR4014] (ab108307) is a rabbit monoclonal antibody that is used to detect CD46 in Western Blot, IHC-P. Suitable for Human samples.
- Specificity confirmed with CD46 knockout cell line validation
pH: 7.2 - 7.4
Preservative: 0.01% Sodium azide
Constituents: 59% PBS, 40% Glycerol (glycerin, glycerine), 0.05% BSA
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:
For more information, read more on recombinant antibodies.
CD46 also known as membrane cofactor protein (MCP) is a type I membrane protein with a molecular weight around 50-70 kDa due to glycosylation variability. This protein serves as a regulatory component in the complement system which protects host cells from damage by complement components. CD46 is widely expressed on almost all nucleated human cells. It plays a role in inactivating C3b and C4b components of the complement cascade preventing autologous complement-mediated damage. The gene coding for CD46 is located on chromosome 1q32 a region known for encoding several complement regulatory proteins.
Beyond its complement regulatory role CD46 acts in immune response modulation and reproduction. It forms a part of a protein complex that involves members such as decay-accelerating factor and complement receptor 1. CD46 also engages in intracellular signaling that affects T cell function and differentiation. In the reproductive context it participates in sperm-oocyte fusion and has a role in trophoblast fusion during placental formation.
CD46 integrates into various signaling pathways including the complement and T cell receptor signaling pathways. In the complement pathway CD46 interacts with C3b and factor I promoting cleavage and inactivation of C3b leading to pathway regulation. Involvement in the T cell receptor pathway hints that CD46 signaling protects against overactive immune responses by promoting a switch to a regulatory T cell phenotype which can modulate immunity and prevent autoimmunity.
CD46 has connections with autoimmune conditions and infectious diseases. For instance alterations in CD46 expression or function can contribute to atypical hemolytic uremic syndrome where dysregulation of the complement pathway occurs. Additionally certain pathogens like Neisseria gonorrhoeae utilize CD46 as a receptor for infection. CD46’s interaction with proteins such as C3b connects it directly to complement-related conditions highlighting its importance in maintaining immune system balance.
We have tested this species and application combination and it works. It is covered by our product promise.
We have not tested this specific species and application combination in-house, but expect it will work. It is covered by our product promise.
This species and application combination has not been tested, but we predict it will work based on strong homology. However, this combination is not covered by our product promise.
We do not recommend this combination. It is not covered by our product promise.
We are dedicated to supporting your work with high quality reagents and we are here for you every step of the way should you need us.
In the unlikely event of one of our products not working as expected, you are covered by our product promise.
Full details and terms and conditions can be found here:
Terms & Conditions.
All lanes: Western blot - Anti-CD46 antibody [EPR4014] (ab108307)
Predicted band size: 44 kDa
ab108307, at 1/500 dilution, staining CD46 in paraffin-embedded human tonsil tissue.
Perform heat mediated antigen retrieval via the pressure cooker method before commencing with IHC staining protocol.
ab108307, at 1/500 dilution, staining CD46 in paraffin-embedded human kidney tissue
Perform heat mediated antigen retrieval via the pressure cooker method before commencing with IHC staining protocol.
All lanes: Western blot - Anti-CD46 antibody [EPR4014] (ab108307) at 1/1000 dilution
Lane 1: MOLT-4 (Human lymphoblastic leukemia cell line) cell lysate at 10 µg
Lane 2: Jurkat (Human T cell leukemia cell line from peripheral blood) cell lysate at 10 µg
Lane 3: HeLa (Human epithelial cell line from cervix adenocarcinoma) cell lysate at 10 µg
Lane 4: K562 (Human chronic myelogenous leukemia cell line from bone marrow) cell lysate at 10 µg
All lanes: Goat anti-rabbit HRP conjugate at 1/2000 dilution
Predicted band size: 44 kDa
ab108307 showing positive staining in human normal placenta tissue.
Perform heat mediated antigen retrieval via the pressure cooker method before commencing with IHC staining protocol.
ab108307 showing positive staining in human normal uterus tissue.
Perform heat mediated antigen retrieval via the pressure cooker method before commencing with IHC staining protocol.
ab108307 showing positive staining in human thyroid gland carcinoma tissue.
Perform heat mediated antigen retrieval via the pressure cooker method before commencing with IHC staining protocol.
ab108307 showing positive staining in human colonic adenocarcinoma tissue.
Perform heat mediated antigen retrieval via the pressure cooker method before commencing with IHC staining protocol.
ab108307 showing positive staining in human breast carcinoma tissue.
Perform heat mediated antigen retrieval via the pressure cooker method before commencing with IHC staining protocol.
ab108307 showing positive staining in human normal breast tissue.
Perform heat mediated antigen retrieval via the pressure cooker method before commencing with IHC staining protocol.
Western blot: Anti-CD46 antibody [EPR4014] (ab108307) staining at 1/1000 dilution, shown in green; Mouse anti-GAPDH antibody [6C5] (Anti-GAPDH antibody [6C5] - Loading Control ab8245) loading control staining at 1/20000 dilution, shown in magenta. In Western blot, ab108307 was shown to bind specifically to CD46. A band was observed at 50-75 kDa in wild-type A549 cell lysates with no signal observed at this size in CD46 knockout cell line. To generate this image, wild-type and CD46 knockout A549 cell lysates were analysed. First, samples were run on an SDS-PAGE gel then transferred onto a nitrocellulose membrane. Membranes were blocked in 3 % 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 800CW and Goat anti-Mouse IgG H&L 680RD at 1/20000 dilution.
All lanes: Western blot - Anti-CD46 antibody [EPR4014] (ab108307) at 1/1000 dilution
Lane 1: Wild-type A549 cell lysate at 20 µg
Lane 2: CD46 knockout A549 cell lysate at 20 µg
Lane 3: HAP1 cell lysate at 20 µg
Lane 4: THP-1 cell lysate at 20 µg
All lanes: Goat anti-Rabbit IgG H&L 800CW and Goat anti-Mouse IgG H&L 680RD at 1/20000 dilution
Performed under reducing conditions.
Image collected and cropped by CiteAb under a CC-BY license from the publication
CD46 western blot using anti-CD46 antibody [EPR4014] ab108307. Publication image and figure legend from Scambi, C., Ugolini, S., et al., 2015, PLoS One, PubMed 25658605.
ab108307 was used in this publication in western blot. This may not be the same as the application(s) guaranteed by Abcam. For a full list of applications guaranteed by Abcam for ab108307 please see the product overview.
Immunoblot analysis of MCP (CD46) of skin biopsies from healthy controls and SSc patients.Protein extract from skin biopsies of 8 SSc patients (4 lesional SSc skin and 4 non-lesional SSc skin) and 8 healthy subjects were analyzed by immunoblot using a specific antibody. Results of a representative experiment of four are shown. Data are expressed as an optical density ratio of MCP (CD46) and β-tubulin.
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