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 Hela cells using PLZF Monoclonal Antibody (green). Red: Actin filaments have been labeled with Alexa Fluor-555 phalloidin.)
WB (Western Blot) (Western Blot analysis using PLZF Monoclonal Antibody against HeLa (1) cell lysate.)
FCM/FACS (Flow Cytometry) (Flow cytometric analysis of Hela cells using Podocalyxin-like 1 Monoclonal Antibody (green) and negative control (purple).)
IHC (Immunohiostchemistry) (Immunohistochemistry analysis of paraffin-embedded lung cancer tissues (left) and kidney tissues (right) with DAB staining using Podocalyxin-like 1 Monoclonal Antibody.)
WB (Western Blot) (Western Blot analysis using Podocalyxin-like 1 Monoclonal Antibody against recombinant protein.)
FCM/FACS (Flow Cytometry) (Flow cytometric analysis of MCF-7 cells using Prohibitin Monoclonal Antibody (blue) and negative control (red).)
IF (Immunofluorescence) (Immunofluorescence analysis of NIH/3T3 cells using Prohibitin 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 rectum cancer tissues with DAB staining using Prohibitin Monoclonal Antibody.)
WB (Western Blot) (Western Blot analysis using Prohibitin Monoclonal Antibody against A431 (1). MCF-7 (2). Jurkat (3). HeLa (4). HepG2 (5). A549 (6). NIH/3T3 (7). Cos7 (8) and PC-12 (9) cell lysate.)
IF (Immunofluorescence) (Confocal immunofluorescence analysis of PC12 cells using Reg I? Monoclonal Antibody (green). Blue: DRAQ5 fluorescent DNA dye.)
IHC (Immunohistochemistry) (Immunohistochemistry analysis of paraffin-embedded human Pancreas tissues with AEC staining using Reg I? Monoclonal Antibody.)
FCM/FACS (Flow Cytometry) (Flow cytometric analysis of HepG2 cells using Rsk-2 Monoclonal Antibody (green) and negative control (red).)
IF (Immunofluorescence) (Immunofluorescence analysis of HepG2 cells using Rsk-2 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 Rsk-2 Monoclonal Antibody against HeLa (1). MCF-7 (2). and HepG2 (3) cell lysate.)
IF (Immunofluorescence) (Immunofluorescence analysis of Hela cells using RUNX1 Monoclonal Antibody (green). Red: Actin filaments have been labeled with Alexa Fluor-555 phalloidin.)
WB (Western Blot) (Western Blot analysis using RUNX1 Monoclonal Antibody against Jurkat cell lysate.)
IHC (Immunohiostchemistry) (Immunohistochemistry analysis of paraffin-embedded human skin carcinoma (left) and breast carcinoma (right). showing cytoplasmic and membrane localization with DAB staining using SRA1 Monoclonal Antibody.)
WB (Western Blot) (Western Blot analysis using SRA1 Monoclonal Antibody against truncated SRA recombinant protein (1). human ovary cancer tissue lysate (2) and A431 cell lysate (3).)
SDS-PAGE (Whole cell lysates were separated by 10% SDS-PAGE, and the membrane was blotted with anti-STAT1 (PTR2109) 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-Annexin II (PTR1321) antibody. The HRP-conjugated Goat anti-M)
SDS-PAGE (Various whole cell lysates were separated by 12% SDS-PAGE, and the membrane was blotted with anti-HDAC1(PTR1326) 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-cadherin Pan(ABT123) antibody. The HRP-conjugated Goat anti-M)
SDS-PAGE (Hela whole cell lysates were separated by 10% SDS-PAGE, and the membrane was blotted with anti-CD44(ABT476) 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-CK16(ABT059) antibody. The HRP-conjugated Goat anti-M)
SDS-PAGE (HaCat whole cell lysates were separated by 10% SDS-PAGE, and the membrane was blotted with anti-CK4(ABT-CK4) 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-Cytokeratin 5/6 (ABT-CK5/052) antibody. The HRP-conjugated Goat anti-M)
SDS-PAGE (Whole cell lysates were separated by 12% SDS-PAGE, and the membrane was blotted with anti-CK7 (ABT437)antibody. The HRP-conjugated Goat anti-M)
SDS-PAGE (MCF7 whole cell lysates were separated by 12% SDS-PAGE, and the membrane was blotted with anti-Claudin 3(ABT509) antibody. The HRP-conjugated Goat anti-M)
SDS-PAGE (MCF7 whole cell lysates were separated by 12% SDS-PAGE, and the membrane was blotted with anti-Claudin 7(ABT441) 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-Lysozyme(ABT191) 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-Melan-A(ABT-Mart1) antibody. The HRP-conjugated Goat anti-M)
IHC (Immunohistochemistry) (Human hippocampus tissue was stained with Anti-Neurofilament (ABT456) Antibody)
IHC (Immunohistochemistry) (Human cerebrum tissue was stained with Anti-Neurofilament (ABT456) Antibody)
IHC (Immunohiostchemistry) (Human appendix tissue was stained with Anti-Neurofilament (ABT456) Antibody)
SDS-PAGE (Various whole cell lysates were separated by 10% SDS-PAGE, and the membrane was blotted with anti-Neurofilament antibody. The HRP-conjugated anti-Mouse IgG antibody was used to detect the antibody.)
SDS-PAGE (Hela whole cell lysates were separated by 10% SDS-PAGE, and the membrane was blotted with anti-Nucleophosmin(ABT210) antibody. The HRP-conjugated Goat anti-M)
IHC (Immunohistochemistry) (Human tonsil tissue was stained with Anti-p120 Catenin (ABT082) Antibody)
IHC (Immunohistochemistry) (Human prostatic adenocarcinoma tissue was stained with Anti-p120 Catenin (ABT082) Antibody)
IHC (Immunohistochemistry) (Human pancreas tissue was stained with Anti-p120 Catenin (ABT082) Antibody)
IHC (Immunohiostchemistry) (Human liver tissue was stained with Anti-p120 Catenin (ABT082) Antibody)
SDS-PAGE (Various whole cell lysates were separated by 8% SDS-PAGE, and the membrane was blotted with anti-p120 Catenin 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-P63 and anti-GAPDH antibody. The HRP-conjugated)
SDS-PAGE (Whole cell lysates of A431 were separated by 8% SDS-PAGE, and the membrane was blotted with anti-p63 antibody. The HRP-conjugated anti-Mouse IgG antibody was used to detect the antibody.)
IHC (Immunohistochemistry) (Human colon tissue was stained with Anti-Proliferating Cell Nuclear Antigen (ABT221) Antibody)
IHC (Immunohistochemistry) (Human colon tissue was stained with Anti-Proliferating Cell Nuclear Antigen (ABT221) Antibody)
IHC (Immunohiostchemistry) (Human colon tissue was stained with Anti-Proliferating Cell Nuclear Antigen (ABT221) Antibody)
SDS-PAGE (Various whole cell lysates were separated by 10% SDS-PAGE, and the membrane was blotted with anti-PCNA antibody. The HRP-conjugated anti-Mouse IgG antibody was used to detect the antibody.)
SDS-PAGE (Various whole cell lysates were separated by 15% SDS-PAGE, and the membrane was blotted with anti-TCL1 (ABT378) 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-Uroplakin III (ABT523) antibody. The HRP-conjugated Goat anti-M)
SDS-PAGE (K562 whole cell lysates were separated by 10% SDS-PAGE, and the membrane was blotted with anti-WT1(ABT-WT1)antibody. The HRP-conjugated Goat anti-M)
SDS-PAGE (P53 knockout and wild-type HEK93 whole cell lysates were separated by 10% SDS-PAGE, and the membrane was blotted with anti-P53 and anti-GAPDH antibody. The HRP-conjugated)
ICC (Immunocytochemistry) (Immunocytochemistry staining of HeLa cells fixed with 4% Paraformaldehyde and using anti-NFIC mouse mAb (dilution 1:200).)
WB (Western Blot) (Western blot detection of NFIC in Hela NE cell lysates using NFIC mouse mAb (1:200 diluted).Predicted band size:56KDa.Observed band size:56KDa.)
WB (Western Blot) (Western blot detection of IkB-alpha(N-terminus) in Jurkat and Hela cell lysates using IkB-alpha(N-terminus) mouse mAb (1:1000 diluted).Predicted band size: 36KDa.Observed band size: 36KDa.)
WB (Western Blot) (Western blot detection of IkB-alpha(N-terminus) in 3T3 cell lysate using IkB-alpha(N-terminus) mouse mAb (1:500 diluted).Predicted band size: 36KDa.Observed band size: 36KDa.)
FCM/FACS (Flow Cytometry) (Flow Cytometry analysis of K562 cells stained with TORC1(N-terminus)(red. 1/100 dilution). followed by FITC-conjugated goat anti-mouse IgG. Blue line histogram represents the isotype control. normal mouse IgG.)
ICC (Immunocytochemistry) (Immunocytochemistry stain of Hela using MECT1/Torc1 mouse mAb (1:300).)
IP (Immunoprecipitation) (Immunoprecipitation analysis of Hela cell lysate using MECT1/Torc1 mouse mAb.)
WB (Western Blot) (Western blot detection of MECT1/Torc1 in Hela and Jurkat lysates using MECT1/Torc1 mouse mAb (1:1000 diluted).Predicted band size: 78KDa.Observed band size: 78KDa.)
SDS-PAGE (MCF7 whole cell lysates were separated by 12% SDS-PAGE, and the membrane was blotted with anti-pS2(ABT265) antibody. The HRP-conjugated Goat anti-M)
SDS-PAGE (Whole cell lysates were separated by 12% SDS-PAGE, and the membrane was blotted with anti-Stathmin (ABT396) 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-PSMD11 (PTR1354) antibody. The HRP-conjugated Goat anti-M)
SDS-PAGE (Hela whole cell lysates were separated by 10% SDS-PAGE, and the membrane was blotted with anti-Caldesmon(ABT125) 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-CD21(ABT-CD21)antibody. The HRP-conjugated Goat anti-M)
WB (Western Blot) (JCHAIN/Ig J Chain Antibody-HEK293T cells were transfected with the pCMV6-ENTRY control (Left lane) or pCMV6-ENTRY IGJ (Right lane) cDNA for 48 hrs and lysed. Equivalent amounts of cell lysates (5 ug per lane) were separated by SDS-PAGE and immunoblotted with anti-IGJ.)
WB (Western Blot) (CTH/Cystathionase Antibody-HEK293T cells were transfected with the pCMV6-ENTRY control (Left lane) or pCMV6-ENTRY CTH (Right lane) cDNA for 48 hrs and lysed. Equivalent amounts of cell lysates (5 ug per lane) were separated by SDS-PAGE and immunoblotted with anti-CTH.)
Application Data (CTH/Cystathionase Antibody-Western blot of extracts (35ug) from 9 different cell lines by using anti-CTH monoclonal antibody (HepG2: human; HeLa: human; SVT2: mouse; A549: human; COS7: monkey; Jurkat: human; MDCK: canine; PC12: rat; MCF7: human).)
IHC (Immunohiostchemistry) (Immunohistochemistry staining of human testis (paraffin sections) using anti-CD271 (NGFR5). Commercially tested by LifeSpan BioSciences.)
The purified antibody is conjugated with fluorescein isothiocyanate (FITC) under optimum conditions. The conjugate is purified by size-exclusion chromatography.
Anti-Mouse CD8 In Vivo Antibody - Low Endotoxin (YTS-169)
Reactivity
Mouse
Applications
Flow Cytometry, Immunohistochemistry
Purity
>95% by SDS-PAGE and HPLC This monoclonal antibody was purified using multi-step affinity chromatography methods such as Protein A or G depending on the species and isotype.
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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