Get accurate results in your research with our Monoclonal Antibodies, which are specially made to target exactly what you require for your research, and will produce consistent, reliable performance in lab tests.
IF (Immunofluorescence) (Immunofluorescence analysis of NIH/3T3 cells using KLHL11 Monoclonal Antibody (green). Blue: DRAQ5 fluorescent DNA dye. Red: Actin filaments have been labeled with Alexa Fluor-555 phalloidin.)
IHC (Immunohiostchemistry) (Immunohistochemistry analysis of paraffin-embedded liver cancer (right) and colon cancer tissues (left) with DAB staining using KLHL11 Monoclonal Antibody.)
WB (Western Blot) (Western Blot analysis using KLHL11 Monoclonal Antibody against HeLa (1) and MCF-7 (2) cell lysate.)
IF (Immunofluorescence) (Immunofluorescence analysis of U251 cells using KLHL22 Monoclonal Antibody (green). Blue: DRAQ5 fluorescent DNA dye. Red: Actin filaments have been labeled with Alexa Fluor-555 phalloidin.)
WB (Western Blot) (Western Blot analysis using KLHL22 Monoclonal Antibody against mouse brain tissues lysate.)
IHC (Immunohiostchemistry) (Immunohistochemistry analysis of paraffin-embedded human Thyroid tissues with AEC staining using Laminin ?-1 Monoclonal Antibody.)
WB (Western Blot) (Western Blot analysis using Laminin ?-1 Monoclonal Antibody against truncated Laminin ?-1-His recombinant protein (1).)
IF (Immunofluorescence) (Confocal immunofluorescence analysis of NTERA-2 cells using LIN-28 Monoclonal Antibody (green). Blue: DRAQ5 fluorescent DNA dye.)
WB (Western Blot) (Western Blot analysis using LIN-28 Monoclonal Antibody against NTERA-2 cell lysate (1).)
FCM/FACS (Flow Cytometry) (Flow cytometric analysis of SK-BR-3 cells using Mammaglobin A Monoclonal Antibody (green) and negative control (purple).)
IF (Immunofluorescence) (Immunofluorescence analysis of Hela cells using Mammaglobin A Monoclonal Antibody (green). Blue: DRAQ5 fluorescent DNA dye. Red: Actin filaments have been labeled with Alexa Fluor-555 phalloidin.)
IHC (Immunohiostchemistry) (Immunohistochemistry analysis of paraffin-embedded mammary cancer tissues with DAB staining using Mammaglobin A Monoclonal Antibody.)
WB (Western Blot) (Western Blot analysis using Mammaglobin A Monoclonal Antibody against Mammaglobin A recombinant protein (1).)
IF (Immunofluorescence) (Confocal immunofluorescence analysis of HepG2 cells using Mcl-1 Monoclonal Antibody (green). Red: Actin filaments have been labeled with DY-554 phalloidin. Blue: DRAQ5 fluorescent DNA dye.)
IHC (Immunohiostchemistry) (Immunohistochemistry analysis of paraffin-embedded human lymphnode tissues with DAB staining using Mcl-1 Monoclonal Antibody.)
WB (Western Blot) (Western Blot analysis using Mcl-1 Monoclonal Antibody against HeLa (1). BCBL-1 (2). Jurkat (3) and HL60 (4) cell lysate.)
IHC (Immunohiostchemistry) (Immunohistochemistry analysis of paraffin-embedded human Placenta tissues with AEC staining using M-CSF Monoclonal Antibody.)
WB (Western Blot) (Western Blot analysis using M-CSF Monoclonal Antibody against human recombinant CSF2 (1) and CSF1 (2).)
FCM/FACS (Flow Cytometry) (Flow cytometric analysis of F9 cells stained with Oct-3/4 Monoclonal Antibody (red). followed by FITC-conjugated goat anti-mouse IgG. Blue line histogram represents the isotype control. normal mouse IgG.)
IF (Immunofluorescence) (Immunofluorescence analysis of COS7 cells using Oct-3/4 Monoclonal Antibody.)
WB (Western Blot) (Western Blot analysis using Oct-3/4 Monoclonal Antibody against F9 cell lysate.)
IHC (Immunohiostchemistry) (Immunohistochemical analysis of paraffin-embedded Human Breast CarcinomaTissue using Ubiquitin Mouse Monoclonal antibody diluted at 1:500)
WB (Western Blot) (Western blot analysis of 1) Hela Cell Lysate. 2) A431 Cell Lysate using Mouse mAb diluted at 1:2.000.)
SDS-PAGE (Various whole cell lysates were separated by 10% SDS-PAGE, and the membrane was blotted with anti-Her-2 (PT1844) antibody. The HRP-conjugated)
SDS-PAGE (Various whole cell lysates were separated by 10% SDS-PAGE, and the membrane was blotted with anti-Tubulin ? (PT2188) antibody. The HRP-conjugated)
SDS-PAGE (Whole cell lysates were separated by 12% SDS-PAGE, and the membrane was blotted with anti-Galectin-9 (PTR1201) antibody. The HRP-conjugated Goat anti-M)
ICC (Immunocytochemistry) (Immunocytochemistry staining of HeLa cells fixed with 4% Paraformaldehyde and using anti-Jak1 mouse mAb (dilution 1:200).)
IP (Immunoprecipitation) (Immunoprecipitation analysis of Hela cell lysates using Jak1 mouse mAb.)
WB (Western Blot) (Western blot analysis of extracts from C6.Ramos.Jurkat and Hela cell lysates using Jak1 mouse mAb (1:1000 diluted).Predicted band size:130KDa.Observed band size:130KDa.)
IP (Immunoprecipitation) (Immunoprecipitation analysis of Hela cell lysates using NUP98 mouse mAb.)
WB (Western Blot) (Western blot detection of NUP98 in Hela.Jurkat and MCF7 cell lysates using NUP98 mouse mAb (1:1000 diluted).Predicted band size: 98kDa.Observed band size: 98kDa.)
WB (Western Blot) (Western blot detection of Prominin-1 in CaCo2 cell lysate using Prominin-1 mouse mAb (1:1000 diluted).Predicted band size:97KDa.Observed band size:133KDa)
WB (Western Blot) (Western blot detection of Prominin-1 expression in CHO-k1 cells non-transfected (A) or transfected (B) with Prominin-1 and using Prominin-1 mouse mAb (1:1000 diluted).Predicted band size:97KDa.Observed band size:133KDa.)
ICC (Immunocytochemistry) (Immunocytochemistry staining of HeLa cells fixed with 4% Paraformaldehyde and using anti-Hsp90 beta mouse mAb (dilution 1:200).)
IP (Immunoprecipitation) (Immunoprecipitation analysis of Hela cell lysates using Hsp90 beta mouse mAb.)
WB (Western Blot) (Western blot detection of Hsp90 beta in Hela.3T3.C6.CHO-K1 and COS7 cell lysates using Hsp90 beta mouse mAb (1:2000 diluted).Exposion time: 4min.Predicted band size:90KDa.Observed band size:90KDa.)
FCM/FACS (Flow Cytometry) (Flow cytometric analysis of MCF-7 cells using NF?B-p105/p50 Monoclonal Antibody (green) and negative control (purple).)
IHC (Immunohiostchemistry) (Immunohistochemistry analysis of paraffin-embedded prostate tissues (left) and bladder cancer tissues (right) with DAB staining using NF?B-p105/p50 Monoclonal Antibody.)
WB (Western Blot) (Western Blot analysis using NF?B-p105/p50 Monoclonal Antibody against K562 (1). Jurkat (2). A431 (3). HeLa (4). THP-1 (5) and MCF-7 (6) cell lysate.)
FCM/FACS (Flow Cytometry) (Flow cytometric analysis of K562 cells using SIRT1 Monoclonal Antibody (green) and negative control (purple).)
IF (Immunofluorescence) (Immunofluorescence analysis of NTERA-2 cells using SIRT1 Monoclonal Antibody (green). Red: Actin filaments have been labeled with Alexa Fluor-555 phalloidin.)
IHC (Immunohiostchemistry) (Immunohistochemistry analysis of paraffin-embedded lung cancer tissues (left) and kidney cancer tissues (right) with DAB staining using SIRT1 Monoclonal Antibody.)
WB (Western Blot) (Western Blot analysis using SIRT1 Monoclonal Antibody against MCF-7 (1). Jurkat (2). HeLa (3). HEK293 (4) and A549 (5) cell lysate.)
SDS-PAGE (Whole cell lysates were separated by 12% SDS-PAGE, and the membrane was blotted with anti-ERG (PTR2282) antibody. The HRP-conjugated Goat anti-M)
SDS-PAGE (Whole cell lysates were separated by 10% SDS-PAGE, and the membrane was blotted with anti-GLUT-1 (PTR2138) antibody. The HRP-conjugated Goat anti-M)
SDS-PAGE (A431 whole cell lysates were separated by 10% SDS-PAGE, and the membrane was blotted with anti-CK15(ABT058) antibody. The HRP-conjugated Goat anti-M)
IHC (Immunohiostchemistry) (Human tonsil tissue was stained with Anti-Cytokeratin 5 (ABT051) Antibody)
SDS-PAGE (Various whole cell lysates were separated by 8% SDS-PAGE, and the membrane was blotted with anti-CK5 antibody. The HRP-conjugated anti-Mouse IgG antibody was used to detect the antibody.)
IHC (Immunohiostchemistry) (Human pancreas tissue was stained with Anti-Neuron-Specific Enolase (ABT-NSE) Antibody)
SDS-PAGE (Various whole cell lysates were separated by 8% SDS-PAGE, and the membrane was blotted with anti-NSE antibody. The HRP-conjugated anti-Mouse IgG antibody was used to detect the antibody.)
SDS-PAGE (Various whole cell lysates were separated by 10% SDS-PAGE, and the membrane was blotted with anti-p120 catenin (ABT-p120) antibody. The HRP-conjugated)
SDS-PAGE (Whole cell lysates were separated by 15% SDS-PAGE, and the membrane was blotted with anti-Uroplakin III (ABT-UPK3) antibody. The HRP-conjugated Goat anti-M)
ICC (Immunocytochemistry) (Immunocytochemistry staining of HeLa cells fixed with -20? Methanol and using GSK-3? mouse mAb (dilution 1:200).)
WB (Western Blot) (Western blot analysis of extracts from A549. Hela. 3T3 and Rat Brain cell lysates using GSK-3? mouse mAb(1:1000 diluted).Predicted band size:46KDa.Observed band size:46KDa.)
IP (Immunoprecipitation) (Immunoprecipitation analysis of Hela cell lysates using GSK-3?.GSK-3? Rabbit mAb was used for the western blot analysis (1:1000 diluted).)
ICC (Immunocytochemistry) (Immunocytochemistry staining of Jurkat cells fixed with -20? Ethanol and using anti-AMACR (C-terminus) mouse mAb (dilution 1:100).)
WB (Western Blot) (Western blot detection of AMACR(C-terminus) in Rat Liver lysates using AMACR(C-terminus) mouse mAb (1:1000 diluted).Predicted band size: 42KDa.Observed band size: 42KDa.)
SDS-PAGE (Whole cell lysates were separated by 10% SDS-PAGE, and the membrane was blotted with anti-FLI1/ERG (ABT-FLI1) antibody. The HRP-conjugated Goat anti-M)
IHC (Immunohistochemistry) (LCN2/Lipocalin 2/NGAL Antibody-Immunohistochemical of paraffin-embedded human prostate tissue using LCN2 Monoclonal Antibody at dilution of 1:200)
IHC (Immunohistochemisry) (LCN2/Lipocalin 2/NGAL Antibody-Immunohistochemical of paraffin-embedded human spleen organization using LCN2 Monoclonal Antibody at dilution of 1:200)
IHC (Immunohiostchemistry) (LCN2/Lipocalin 2/NGAL Antibody-Anti-LCN2/Lipocalin 2/NGAL antibody IHC staining of human spleen. Immunohistochemistry of formalin-fixed, paraffin-embedded tissue after heat-induced antigen retrieval. Antibody concentration 20 ug/ml.)
WB (Western Blot) (LCN2/Lipocalin 2/NGAL Antibody-All lanes:Mouse anti-human Neutrophil gelatinase-associated lipocalin monoclonal antibody at 1ug/ml Lane 1:NGAL transfected 293 cell lysate Predicted band size : 22 kDa Observed band size : 25 kDa)
WB (Western Blot) (Various lysates were subjected to SDS PAGE followed by western blot with GPC3 antibody (RHE84602) at 1?ug/ml.Lane 1: Human GPC3 transfected HEK293 cell lysateLane 2: Non-transfected HEK293 cell lysateSecond Ab: Goat Anti-Human IgG H&L Polyclonal antibody, HRP (PHB96431) at 0.1 ug/mL.Predict MW: 63 kDa)
FCM/FACS (Flow Cytometry) (Flow-cytometry using anti-human GPC3 antibody.Human Jurkat cell line were stained with an irrelevant antibody (Blue Histogram) or an anti-human GPC3 antibody monoclonal antibody (Catalog # RHE84602 ,Green Histogram) at a concentration of 5 ?ug/ml for 30 mins at RT. After washing, bound antibody was detected using a FITC conjugated goat anti-human antibody (Catalog # PHB96441) and cells analysed on a NovoCyte Flow Cytometer.)
FCM/FACS (Flow Cytometry) (Flow-cytometry using anti-human GPC3 antibody.HepG2 cells were stained with an irrelevant antibody (Blue Histogram) or an anti-human GPC3 antibody monoclonal antibody (Catalog # RHE84602 ,Green Histogram) at a concentration of 5 ?ug/ml for 30 mins at RT. After washing, bound antibody was detected using a FITC conjugated goat anti-human antibody (Catalog # PHB96441) and cells analysed on a NovoCyte Flow Cytometer.)
FCM/FACS (Flow Cytometry) (Flow-cytometry using anti-human GPC3 antibody.GPC3 Transfected CHO cells were stained with an irrelevant antibody (Blue Histogram) or an anti-human GPC3 antibody monoclonal antibody (Catalog # RHE84602 ,Green Histogram) at a concentration of 5 ?ug/ml for 30 mins at RT. After washing, bound antibody was detected using a FITC conjugated goat anti-human antibody (Catalog # PHB96441) and cells analysed on a NovoCyte Flow Cytometer.)
Bioactivity (Detects Human GPC3 in indirect ELISAs.)
>95% by SDS-PAGE Protein A or G purified from cell culture supernatant.
Pricing
What are Monoclonal Antibodies?
Monoclonal antibodies are specialized laboratory-produced proteins developed for binding to specific biological antigens or other molecular targets. Since they come from a single cell (or clone), they are especially consistent and accurate in the data they are involved in producing.
This type of antibody material has been shown to be a powerful tool in finding and subsequently destroying harmful cells in an organism, such as those found in cancers or various autoimmune diseases. This makes them excellent aids in medical testing and research, which is why they are so widely used.
AAA Biotech offers a comprehensive range of high-quality monoclonal antibodies that perform effectively in various laboratory tests, including (amongst others) ELISA, western blotting, immunohistochemistry, and flow cytometry. All of the products in our catalog are thoroughly quality tested to make sure that they are reliable and will consistently perform well in your research.
What Are The Uses of Monoclonal Antibodies
Monoclonal antibodies are used in many lab tests, including (amongst others) ELISA, western blotting, immunohistochemistry, and flow cytometry.
ELISA is a test that helps detect a specific substance/analyte in a sample. It uses antibodies (often monoclonal) bound to a solid surface (such as the well of a microplate) to “capture” the substance/analyte in the sample and immobilize it so that the detection antibody component can then bind to it and produce a signal, which can then be measured.
Western blotting identifies specific proteins in a sample. The sample is first separated on a gel, and then antibodies are applied that will typically bind to the target, which will all be localized to a single band in a lane.
Immunohistochemistry helps locate specific proteins in cells or tissue samples using antibodies.
Flow cytometry looks at and sorts cells. It uses antibodies that are conjugated to reporter molecules called “fluorophores”, which, under special lights, emit light themselves, which can then be measured by a detector instrument.
How Monoclonal Antibodies Are Used as Medicine?
Please note that all of the products listed in AAA Biotech’s catalog are strictly for research-use only (RUO).
Monoclonal antibodies can also be used as therapeutic/medical treatments, particularly in the context of cancers. They are designed to find and bind to specific cells or proteins, helping the immune system recognize and attack the cancer. These treatments work in different ways, such as:
Radioimmunotherapy attaches a small amount of radioactive molecule to the antibody, so it delivers the radiation directly to the cancer cells that the antibody is specifically binding to.
Antibody-directed enzyme prodrug therapy uses antibodies that are specifically bound to special enzymes. These enzymes activate a harmless drug in the body and turn it into a cancer-killing drug only near the cancer cells—this helps avoid harming healthy cells.
Immunoliposomes are tiny “bubbles” filled with medicine/drug and coated with antibodies. They carry the drug straight to the cancer cells.
Why Buy Monoclonal Antibodies From Us?
At AAA Biotech, we provide high-performance monoclonal antibodies designed to support a wide range of research needs.
1. Validated for Versatile Applications
The antibodies in our catalog are extensively validated and compatible with multiple techniques, including (but not limited to) ELISA, flow cytometry (FC), immunocytochemistry (ICC), immunofluorescence (IF), immunohistochemistry (IHC), immunoprecipitation (IP), and western blotting (WB).
2. Wide Selection & Specialized Options
We offer antibodies for common and rare species, that are available in various conjugated forms, and also in recombinant formats. Essentially, there is almost anything one might need to meet their experimental model’s requirements.
3. High-Quality Proteins
Our proteins meet high purity standards—90% or more as confirmed by SDS-PAGE. Many are available with tags like His, Flag, GST, or MBP, and we also supply native and biologically active proteins for functional studies.
Frequently Asked Questions
1. Are your monoclonal antibodies validated for specific applications?
Yes, our antibodies are tested and validated for use in methods such as ELISA, western blot, IHC, flow cytometry, and more. Refer to specific product pages or datasheets for individual product information.
2. How do I choose the right monoclonal antibody for my application?
Review the product details directly for application validation, species reactivity, and target information. You may also contact our support team at any time for help.
3. How quickly can I receive my order?
Most orders are processed and shipped within 1–3 business days, depending on product availability and your shipping location.
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