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.
SDS-PAGE (Various whole cell lysates were separated by 8% SDS-PAGE, and the membrane was blotted with anti-Actin, sarcomeric muscle(ABT-SCA)antibody. The HRP-conjugated Goat anti-M)
Application Data (HuVEC whole cell lysates were separated by 10% SDS-PAGE, and the membrane was blotted with anti-CD105(ABT-CD105) antibody. The HRP-conjugated Goat anti-M)
SDS-PAGE (Various whole cell lysates were separated by 10% SDS-PAGE, and the membrane was blotted with anti-CD163 (ABT-CD163) 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-CK14 (ABT049) antibody. The HRP-conjugated Goat anti-M)
SDS-PAGE (Whole cell lysates were separated by 15% SDS-PAGE, and the membrane was blotted with anti-E-Cadherin (ABT181) antibody. The HRP-conjugated Goat anti-M)
Standard Curve (Sample) (Standard Curve for Human Serum Albumin (Analyte: Human Serum Albumin protein ); using Capture Antibody Mouse monoclonal [1A8-C5-B4] to Human Serum Albumin at 8 ug/ml and Detector Antibody Rabbit polyclonal antiserum to Human Serum Albumin.)
WB (Western Blot) (Western blot detection of Human Serum Albumin in 0.5nl human serum and 5ng ALB Recombinant antigens cell lysates using Human Serum Albumin mouse mAb (1:1000 diluted).Predicted band size:67KDa.Observed band size:67KDa.)
FCM/FACS (Flow Cytometry) (Flow Cytometry analysis of Jurkat cells stained with SMAD5 (red. 1/100 dilution). followed by FITC-conjugated goat anti-mouse IgG. Black line histogram represents the isotype control. normal mouse IgG.)
ICC (Immunocytochemistry) (Immunocytochemistry of HeLa cells using anti-SMAD5 (C-terminus) mouse mAb diluted 1:75.)
WB (Western Blot) (Western blot detection of SMAD5 (C-terminus) in Hela.Jurkat and K562 cell lysates using SMAD5 (C-terminus) mouse mAb (1:1000 diluted).Predicted band size:52KDa.Observed band size:60KDa.)
ICC (Immunocytochemistry) (Immunocytochemistry staining of HeLa cells fixed with 4% Paraformaldehyde and using GTF2H1 mouse mAb (dilution 1:50).)
IP (Immunoprecipitation) (Immunoprecipitation analysis of Hela cell lysates using GTF2H1 mouse mAb.)
WB (Western Blot) (Western blot detection of GTF2H1 in Hela.Hela NE and Jurkat cell lysates using GTF2H1 mouse mAb (1:300 diluted).Predicted band size: 62KDa.Observed band size: 62KDa.)
IF (Immunofluorescence) (Immunofluorescent analysis of Hela cells fixed fixed by anhydrous methanol at -20? and using SirT2 (200474.dilution 1:50) mouse mAb (green) and Histone H3.1 (Phospho-Ser10)(310045.dilution 1:200) Rabbit pAb (red).)
WB (Western Blot) (Western blot detection of SirT2 in PC-12. Rat Brain and Mouse Brain cell lysates using SirT2 mouse mAb (1:1000 diluted). Predicted band size: 39.43KDa. Observed band size:39.43KDa.)
IF (Immunofluorescence) (Immunofluorescence analysis of NIH/3T3 cells using Arg 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 Arg Monoclonal Antibody against HEK293T cells transfected with the pCMV6-ENTRY control (1) and pCMV6-ENTRY ABL2 cDNA (2).)
IHC (Immunohistochemistry) (Immunohistochemical analysis of paraffin-embedded human breast cancer tissues (left) and human esophageal cancer tissues (right) using CD133 mouse mAb with DAB staining.)
WB (Western Blot) (Western blot analysis using TGFBR3 mouse mAb against Jurkat (1), HeLa (2), MCF-7 (3), F9 (4), SK-N-SH (5), and NIH3T3 (6) cell lysate.)
IF (Immunofluorescence) (Immunofluorescence analysis of HeLa cells using HAS2 mouse mAb (green).Blue: DRAQ5 fluorescent DNA dye. Red: Actin filaments have been labeled with Alexa Fluor-555 phalloidin.)
IHC (Immunohistochemisry) (Immunohistochemical analysis of paraffin-embedded ovarian cancer tissues using HAS2 mouse mAb with DAB staining.)
WB (Western Blot) (Western blot analysis using HAS2 mouse mAb against NTERA-2 (1),HEK293 (2) cell lysate.)
WB (Western Blot) (Figure 1: Western blot analysis using HAS2 mAb against human HAS2 recombinant protein. (Expected MW is 37.5 kDa))
IHC (Immunohistochemistry) (Figure 1: Immunohistochemical analysis of paraffin-embedded human lymph node (A), esophagus (B), lung cancer (C), rectum cancer (D), showing nuclear localization using KI67 mouse mAb with DAB staining.)
IHC (Immunohiostchemistry) (Immunohistochemical analysis of paraffin-embedded human lymph tissue (A), glioma tissue (B) and cerebellum tissue (C), showing membrane localization using Dynamin1 mouse mAb with DAB staining)
WB (Western Blot) (Figure 1: Western blot analysis using Dynamin1 mouse mAb against C6 (1), NIH/3T3 (2), SKN-SH (3), LN18 (4), SHSY5Y (5) cell lysate and rat brain tiisues lysate (6).)
SDS-PAGE (Hela whole cell lysates were separated by 10% SDS-PAGE, and the membrane was blotted with anti-GST-Pi(ABT256) 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-Perforin (ABT355)antibody. The HRP-conjugated Goat anti-M)
SDS-PAGE (Various whole cell lysates were separated by 10% SDS-PAGE, and the membrane was blotted with anti-Stathmin (ABT347) 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-Prostein (PTR1344/1345) antibody. The HRP-conjugated Goat anti-M)
SDS-PAGE (Various whole cell lysates were separated by 10% SDS-PAGE, and the membrane was blotted with anti-CD9 (PTR1357) 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-Cytokeratin 10 (PTR1360/056) antibody. The HRP-conjugated Goat anti-Ra)
SDS-PAGE (Whole cell lysates were separated by 10% SDS-PAGE, and the membrane was blotted with anti-Cytokeratin 10 (PTR1360) antibody. The HRP-conjugated Goat anti-Ra)
IHC (Immunohistochemistry) (Human smooth muscle tissue was stained with anti-calponin-1(ABT133) antibody.)
IHC (Immunohiostchemistry) (Human appendix tissue was stained with anti-calponin-1(ABT133) antibody.)
SDS-PAGE (Various whole cell lysates were separated by 10% SDS-PAGE, and the membrane was blotted with anti-Calponin-1 antibody. The HRP-conjugated anti-Mouse IgG antibody was used to detect the antibody.)
IF (Immunofluorescence) (Confocal immunofluorescent analysis of Jurkat cells labeling CD3 (ABT295) mouse mAb followed by Goat Anti-mouse IgG H&L (FITC Conjugate) sec)
SDS-PAGE (Various whole cell lysates were separated by 10% SDS-PAGE, and the membrane was blotted with anti-CD68 (ABT-CD68) 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-HDAC6 (ABT-HDAC6)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-Neurofilament (ABT208)antibody. The HRP-conjugated Goat anti-M)
SDS-PAGE (LN18 whole cell lysates were separated by 12% SDS-PAGE, and the membrane was blotted with anti-INI-1(ABT-INI1) antibody. The HRP-conjugated Goat anti-M)
SDS-PAGE (HL60 whole cell lysates were separated by 12% SDS-PAGE, and the membrane was blotted with anti-MPO(ABT-MPO)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-Neurofilament (ABT356)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-Nucleophosmin(ABT486)antibody. The HRP-conjugated Goat anti-M)
SDS-PAGE (Various whole cell lysates were separated by 10% SDS-PAGE, and the membrane was blotted with anti-p57kip2 (ABT214) antibody. The HRP-conjugated Goat anti-M)
IHC (Immunohistochemistry) (Human breast carcinoma tissue was stained with Anti-Progesterone Receptor (ABT005) Antibody)
IHC (Immunohistochemistry) (Human breast carcinoma tissue was stained with Anti-Progesterone Receptor (ABT005) Antibody)
IHC (Immunohiostchemistry) (Human breast carcinoma tissue was stained with Anti-Progesterone Receptor (ABT005) Antibody)
SDS-PAGE (Whole cell lysates of Hela were separated by 8% SDS-PAGE, and the membrane was blotted with anti-PR 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-PSA (ABT114)antibody. The HRP-conjugated Goat anti-M)
IHC (Immunohistochemistry) (Human rectal carcinoma tissue was stained with Anti-SOX9 (ABT-SOX9) Antibody)
IHC (Immunohistochemistry) (Human gastric adenocarcinoma tissue was stained with Anti-SOX9 (ABT-SOX9) Antibody)
IHC (Immunohiostchemistry) (Human colon carcinoma tissue was stained with Anti-SOX9 (ABT-SOX9) Antibody)
SDS-PAGE (Various whole cell lysates were separated by 10% SDS-PAGE, and the membrane was blotted with anti-SOX9 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-Vimentin and anti-GAPDH antibody. The HRP-conjugated)
SDS-PAGE (K562 whole cell lysates were separated by 10% SDS-PAGE, and the membrane was blotted with anti-MAGE-C1(ABT339)antibody. The HRP-conjugated Goat anti-M)
Monoclonal Antibody to Follicle Stimulating Hormone Beta (FSHb)
Reactivity
Human, Pig
Applications
Immunoprecipitation, Immunocytochemistry, Immunohistochemistry, Western Blot
Purity
Protein A + Protein G affinity chromatography
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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