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.
IHC (Immunohiostchemistry) (Immunohistochemistry analysis of paraffin-embedded human gastric cancer (left) and normal gastric tissues (right) with DAB staining using Cerberus Monoclonal Antibody.)
WB (Western Blot) (Western Blot analysis using Cerberus Monoclonal Antibody against CER1 (aa18-267)-hIgGFc transfected HEK293 cell lysate (1).)
IHC (Immunohiostchemistry) (Immunohistochemistry analysis of paraffin-embedded lung cancer (left) and ovary tumour tissues (right) with DAB staining using Cyclin B1 Monoclonal Antibody.)
WB (Western Blot) (Western Blot analysis using Cyclin B1 Monoclonal Antibody against HeLa (1). Jurkat (2). K562 (3) and PC-12 (4) cell lysate.)
FCM/FACS (Flow Cytometry) (Flow cytometric analysis of PACN-1 cells using Cytokeratin 15 Monoclonal Antibody (green) and negative control (purple).)
IF (Immunofluorescence) (Immunofluorescence analysis of HepG2(left) and PACN-1 (right) cells using Cytokeratin 15 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 Tonsil tissues with AEC staining using Cytokeratin 15 Monoclonal Antibody.)
WB (Western Blot) (Western Blot analysis using Cytokeratin 15 Monoclonal Antibody against A431 cell lysate.)
IHC (Immunohiostchemistry) (Immunohistochemistry analysis of paraffin-embedded human lymph tissue (A). glioma tissue (B) and cerebellum tissue (C). showing membrane localization with DAB staining using Dynamin I Monoclonal Antibody.)
WB (Western Blot) (Western Blot analysis using Dynamin I Monoclonal Antibody against C6 (1). NIH/3T3 (2). SKN-SH (3). LN18 (4). SHSY5Y (5) cell lysate and rat brain tiisues lysate (6).)
IF (Immunofluorescence) (Immunofluorescence analysis of GC7901 cells using EPO 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 EPO Monoclonal Antibody against HEK293 (1) and EPO-hIgGFc transfected HEK293 (2) cell lysate.)
IF (Immunofluorescence) (Confocal immunofluorescence analysis of Hela cells using Fer Monoclonal Antibody (green). Red: Actin filaments have been labeled with Alexa Fluor-555 phalloidin. Blue: DRAQ5 fluorescent DNA dye.)
IHC (Immunohiostchemistry) (Immunohistochemistry analysis of paraffin-embedded human kidney tissues with AEC staining using Fer Monoclonal Antibody.)
WB (Western Blot) (Western Blot analysis using Fer Monoclonal Antibody against NIH/3T3 (1). A549 (2) and SK-MEL-5 (3) cell lysate.)
IHC (Immunohiostchemistry) (Immunohistochemistry analysis of paraffin-embedded human colon cancer (A). gastric cancer (B) and rectal cancer (C) tissues with DAB staining using FoxA2 Monoclonal Antibody.)
WB (Western Blot) (Western Blot analysis using FoxA2 Monoclonal Antibody against A549 (1) cell lysate.)
IF (Immunofluorescence) (Immunofluorescence analysis of RAJI cells using CD1A Monoclonal Antibody (green). Blue: DRAQ5 fluorescent DNA dye.)
IHC (Immunohiostchemistry) (Immunohistochemistry analysis of paraffin-embedded cervical cancer tissues (left) and colon cancer tissues (right) with DAB staining using CD1A Monoclonal Antibody.)
WB (Western Blot) (Western Blot analysis using CD1A Monoclonal Antibody against K562 (1). RAJI (2). and MOLT4 (3) cell lysate.)
FCM/FACS (Flow Cytometry) (Flow cytometric analysis of Hela cells using Fyn Monoclonal Antibody (green) and negative control (purple).)
IF (Immunofluorescence) (Immunofluorescence analysis of U251 cells using Fyn 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 breast cancer tissues (left) and brain tissues (right) with DAB staining using Fyn Monoclonal Antibody.)
WB (Western Blot) (Western Blot analysis using Fyn Monoclonal Antibody against HeLa cell lysate.)
IF (Immunofluorescence) (Confocal immunofluorescence analysis of Hela cells using GABP-? Monoclonal Antibody (green). Red: Actin filaments have been labeled using DY-554 phalloidin. Blue: DRAQ5 fluorescent DNA dye.)
WB (Western Blot) (Western Blot analysis using GABP-? Monoclonal Antibody against HeLa (1). A549 (2). MCF-7 (3). NIH/3T3 (4) and SMMC-7721 (5) cell lysate.)
IHC (Immunohiostchemistry) (Immunohistochemistry analysis of paraffin-embedded human brain tissue (A) and stomach tissue (B). showing cytoplasmic localization with DAB staining using IRE1? Monoclonal Antibody.)
WB (Western Blot) (Western Blot analysis using IRE1? Monoclonal Antibody against Raji (1). A431 (2). Jurkat (3). HeLa(4) and HEK293 (5) cell lysate.)
IF (Immunofluorescence) (Immunofluorescence analysis of NTERA-2 cells using JMJD2A Monoclonal Antibody (green). Red: Actin filaments have been labeled with Alexa Fluor-555 phalloidin.)
IHC (Immunohiostchemistry) (Immunohistochemistry analysis of paraffin-embedded colon cancer tissues (left) and human larynx cancer tissues (right) with DAB staining using JMJD2A Monoclonal Antibody.)
WB (Western Blot) (Western Blot analysis using JMJD2A Monoclonal Antibody against HEK293 (1) and JMJD2A-hIgGFc transfected HEK293 (2) cell lysate.)
IF (Immunofluorescence) (Immunofluorescence analysis of NIH/3T3 cells using KLHL1 Monoclonal Antibody (green). Red: Actin filaments have been labeled with Alexa Fluor-555 phalloidin.)
WB (Western Blot) (Western Blot analysis using KLHL1 Monoclonal Antibody antiobdy against KLHL1 recombinant protein.)
FCM/FACS (Flow Cytometry) (Flow cytometric analysis of 3T3/L1 cells using KLHL13 Monoclonal Antibody (green) and negative control (purple).)
IF (Immunofluorescence) (Immunofluorescence analysis of NTERA-2 cells (left) and U251 (right) cells using KLHL13 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 brain tissues (left) and pancreas tissues (right) with DAB staining using KLHL13 Monoclonal Antibody.)
WB (Western Blot) (Western Blot analysis using KLHL13 Monoclonal Antibody against HeLa (1) and MCF-7 (2) cell lysate.)
IF (Immunofluorescence) (Immunofluorescence analysis of Hela cells using LMP7A 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 intima cancer tissues with DAB staining using LMP7A Monoclonal Antibody.)
WB (Western Blot) (Western Blot analysis using LMP7A Monoclonal Antibody against HeLa (1). MCF-7 (2). A431 (3). RAJI (4). MOTL4 (5) and PC-12 (6) cell lysate.)
IF (Immunofluorescence) (Confocal immunofluorescence analysis of COS cells using LPP Monoclonal Antibody (green). Red: Actin filaments have been labeled using DY-554 phalloidin. Blue: DRAQ5 fluorescent DNA dye.)
IHC (Immunohiostchemistry) (Immunohistochemistry analysis of paraffin-embedded human small intestine with DAB staining using LPP Monoclonal Antibody.)
WB (Western Blot) (Western Blot analysis using LPP Monoclonal Antibody against HeLa (1). NIH/3T3 (2). COS (3). Caki (4). MCF-7 (5). HepG2 (6) and SMMC-7721 (7) cell lysate.)
IF (Immunofluorescence) (Confocal immunofluorescence analysis of PC-12 cells using Trk A Monoclonal Antibody (green). showing membrane and cytoplasmic localization. Blue: DRAQ5 fluorescent DNA dye.)
WB (Western Blot) (Western Blot analysis using Trk A Monoclonal Antibody against extracellular domain of human Trk A (aa33-423).)
FCM/FACS (Flow Cytometry) (Flow cytometric analysis of Jurkat cells stained with Smad5 Monoclonal Antibody (red). followed by FITC-conjugated goat anti-mouse IgG. Black line histogram represents the isotype control. normal mouse IgG.)
IF (Immunofluorescence) (Immunofluorescence analysis of HeLa cells using Smad5 Monoclonal Antibody.)
WB (Western Blot) (Western Blot analysis using Smad5 Monoclonal Antibody against mouse testis lysate.)
ICC (Immunocytochemistry) (Immunocytochemistry staining of HeLa cells fixed with 4% Paraformaldehyde and using anti-TBL1X mouse mAb (dilution 1:100).)
WB (Western Blot) (Western blot detection of TBL1X in SW480 cell lysates using TBL1X mouse mAb (1:1000 diluted).Predicted band size:58KDa.Observed band size:58KDa.)
IP (Immunoprecipitation) (Immunoprecipitation analysis of Hela cell lysates using Dynactin 1 mouse mAb.)
WB (Western Blot) (Western blot detection of Dynactin 1 in K562.MCF7.293T and Hela cell lysates using Dynactin 1 mouse mAb (1:500 diluted).Predicted band size:150KDa.Observed band size: 150KDa.)
ICC (Immunocytochemistry) (Immunocytochemistry of HeLa cells using anti-Protein Phosphatase 4C mouse mAb diluted 1:200.)
IHC (Immunohiostchemistry) (IHC of paraffin-embedded human breast cancer using anti-Protein Phosphatase 4C mouse mAb diluted 1/500-1/1000.)
WB (Western Blot) (Western blot detection of Protein Phosphatase 4C in Hela and Jurkat cell lysates using Protein Phosphatase 4C mouse mAb (1:200 diluted).Predicted band size: 34KDa.Observed band size: 34KDa.)
ICC (Immunocytochemistry) (Immunocytochemistry staining of C6 cells fixed by anhydrous methanol for 2 h at -20? and using anti-CSK mouse mAb (dilution 1:50).)
WB (Western Blot) (Western blot detection of CSK in C6 and Jurkat cell lysates using CSK mouse mAb (1:1000 diluted).Predicted band size:50KDa.Observed band size:50KDa.)
IF (Immunofluorescence) (Immunofluorescent analysis of Hela cells fixed fixed by anhydrous methanol at -20? and using FAK mouse mAb (dilution 1:200).)
WB (Western Blot) (Western blot detection of FAK in COS7.HUVEC.A549 and Hela cell lysates using FAK mouse mAb (1:1000 diluted).Predicted band size: 125KDa.Observed band size:125KDa.)
IP (Immunoprecipitation) (Immunoprecipitation analysis of THP-1 cell lysates using CD31 mouse mAb.)
WB (Western Blot) (Western blot detection of CD31 in THP-1 cell lysate using CD31 mouse mAb (1:1000 diluted).Predicted band size: 130KDa.Observed band size: 130KDa.)
ICC (Immunocytochemistry) (Immunocytochemistry staining of HeLa cells fixed in 1% Paraformaldehyde and using RPA70 mouse mAb (dilution 1:100).)
IP (Immunoprecipitation) (Immunoprecipitation analysis of Hela cell lysates using RPA70 mouse mAb.)
WB (Western Blot) (Western blot detection of RPA70 in HUVEC.Ha.MCF7 and A549 cell lysates using RPA70 mouse mAb (1:2000 diluted).Predicted band size:70KDa.Observed band size:70KDa.)
WB (Western Blot) (Western blot detection of RPA70 in Hela.A431.MCF7.COS7.HT1080 and K562 cell lysates using RPA70 mouse mAb (1:1000 diluted).Predicted band size:70KDa.Observed band size:70KDa.)
WB (Western Blot) (Western blot detection of RPA70 in Hela.293T.C6.3T3 and K562 cell lysates using RPA70 mouse mAb (1:1000 diluted).Predicted band size:70KDa.Observed band size:70KDa.)
ICC (Immunocytochemistry) (Immunocytochemistry staining of HeLa cells fixed in 1% Paraformaldehyde and then permeabilized in 0.1% Triton X-100.next using WDR77 mouse mAb (dilution 1:100).)
WB (Western Blot) (Western blot detection of WDR77 in C6.3T3 and K562 cell lysates using WDR77 mouse mAb (1:1000 diluted).Predicted band size:42KDa.Observed band size:42KDa.)
IF (Immunofluorescence) (Immunofluorescent analysis of 3T3 cells fixed by anhydrous methanol for 2 h at -20? and using anti-JNK1 mouse mAb (dilution 1:100).)
WB (Western Blot) (Western blot detection of JNK1 in CHO-K1 cell lysate(B) and CHO-K1 transfected by JNK1-fragment fusion protein(A) cell lysate using JNK1 mouse mAb (1:2000 diluted).Predicted band size:46.54KDa.Observed band size:46.54KDa.)
WB (Western Blot) (Western blot detection of JNK1 in C6 and 3T3 cell lysates using JNK1 mouse mAb (1:1000 diluted).Predicted band size:46.54KDa.Observed band size:46KDa.)
ICC (Immunocytochemistry) (Immunocytochemistry staining of HeLa cells fixed with 4% Paraformaldehyde and using DDX3 mouse mAb (dilution 1:200).)
IP (Immunoprecipitation) (Immunoprecipitation analysis of Hela cell lysates using DDX3 mouse mAb.)
WB (Western Blot) (Western blot detection of DDX3 in Hela.3T3.C6.COS7.K562 and Jurkat cell lysate using DDX3 mouse mAb (1:1000 diluted).Predicted band size: 75KDa.Observed band size: 75KDa.)
FCM/FACS (Flow Cytometry) (Flow cytometric analysis of PC-2 cells using N-cadherin Monoclonal Antibody (green) and negative control (purple).)
IF (Immunofluorescence) (Immunofluorescence analysis of A431 cells using N-cadherin Monoclonal Antibody (green). Blue: DRAQ5 fluorescent DNA dye.)
IHC (Immunohiostchemistry) (Immunohistochemistry analysis of paraffin-embedded human lung cancer (A). colon cancer (B). ovarian cancer (C) and mammary cancer(D) with DAB staining using N-cadherin Monoclonal Antibody.)
WB (Western Blot) (Western Blot analysis using N-cadherin Monoclonal Antibody against A431 (1). NIH/3T3 (2). HeLa (3). C6 (4) and LNCap (5) cell lysate.)
FCM/FACS (Flow Cytometry) (Flow cytometric analysis of Jurkat cells using NM23-H1 Monoclonal Antibody (green) and negative control (purple).)
IF (Immunofluorescence) (Immunofluorescence analysis of Hela cells using NM23-H1 Monoclonal Antibody (green). Red: Actin filaments have been labeled with Alexa Fluor-555 phalloidin. Blue: DRAQ5 fluorescent DNA dye.)
IHC (Immunohiostchemistry) (Immunohistochemistry analysis of paraffin-embedded human Placenta tissues with AEC staining using NM23-H1 Monoclonal Antibody.)
WB (Western Blot) (Western Blot analysis using NM23-H1 Monoclonal Antibody against NME1-hIgGFc transfected HEK293 cell lysate.)
FCM/FACS (Flow Cytometry) (Flow cytometric analysis of NIH/3T3 cells using Rab 25 Monoclonal Antibody (green) and negative control (purple).)
IF (Immunofluorescence) (Immunofluorescence analysis of A549 cells using Rab 25 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 esophagus tissues (left) and human lung cancer (right) with DAB staining using Rab 25 Monoclonal Antibody.)
WB (Western Blot) (Western Blot analysis using Rab 25 Monoclonal Antibody against MCF-7 (1). T47D (2) and GC7901 (3) cell lysate.)
FCM/FACS (Flow Cytometry) (Flow cytometric analysis of K562 cells using Smad4 Monoclonal Antibody (green) and negative control (purple).)
IF (Immunofluorescence) (Immunofluorescence analysis of NIH/3T3 cells using Smad4 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 lung cancer tissues with DAB staining using Smad4 Monoclonal Antibody.)
WB (Western Blot) (Western Blot analysis using Smad4 Monoclonal Antibody against A431 (1). SK-N-SH (2). K562 (3). HepG2 (4) and HUVE12 (5) cell lysate.)
IHC (Immunohistochemisry) (Immunohistochemical analysis of paraffin-embedded Human Brain Tissue using Beclin-1 Mouse mAb diluted at 1:200.)
WB (Western Blot) (Western blot analysis of lysates from 1) 293T Cell Lysate. 2) C2C12 Cell Lysate. 3) Rat Brain Tissue cells. (Green) primary antibody was diluted at 1:1000. 4 degree over night. secondary antibodywas diluted at 1:10000. 37 degree 1hour. (Red) Actin ? Polyclonal Antibody antibody was diluted at 1:5000 as loading control. 4 degree over night.secondary antibodywas diluted at 1:10000. 37 degree 1hour.)
WB (Western Blot) (Western blot analysis of 1) 293T Cell Lysate. 2) C2C12 Cell Lysate. 3) Rat Brain Tissue Lysate using Beclin-1 Mouse mAb diluted at 1:2000.)
SDS-PAGE (Various whole cell lysates were separated by 8% SDS-PAGE, and the membrane was blotted with anti-R-Cadherin (PT2127) antibody. The HRP-conjugated)
SDS-PAGE (Whole cell lysates were separated by 15% SDS-PAGE, and the membrane was blotted with anti-PKC(PTR1190) antibody. The HRP-conjugated Goat anti-M)
SDS-PAGE (Lncap whole cell lysates were separated by 10% SDS-PAGE, and the membrane was blotted with anti-AR(ABT101) 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-CD35(ABT-CD35) antibody. The HRP-conjugated Goat anti-M)
IHC (Immunohistochemistry) (Human tonsil tissue was stained with Anti-CD44 (ABT147) Antibody)
IHC (Immunohiostchemistry) (Human tonsil tissue was stained with Anti-CD44 (ABT147) Antibody)
SDS-PAGE (Various whole cell lysates were separated by 10% SDS-PAGE, and the membrane was blotted with anti-CD44 antibody. The HRP-conjugated anti-Mouse IgG antibody was used to detect the antibody.)
SDS-PAGE (Whole cell lysates were separated by 10% SDS-PAGE, and the membrane was blotted with anti-CD61 (ABT032)antibody. The HRP-conjugated Goat anti-M)
Immunofluorescence, Western Blot, Immunohistochemistry
Purity
Protein G
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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