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 (Immunohistochemisry) (Immunohistochemical analysis of OSGEP protein in paraffin embedded Adenocarcinoma of Human colon tissue using OSGEP antibody)
WB (Western Blot) (Western Blot analysis of HEK293T cell lysates (5 ug) transfected with either recombinant OSGEP protein (Right) or empty vector (Left) detected with OSGEP antibody)
IF (Immunofluorescence) (Immunofluorescent staining of COS7 cells transiently transfected with recombinant OSGEP protein using OSGEP antibody)
IF (Immunofluorescence) (Immunofluorescent staining of COS7 cells transiently transfected with recombinant HSD17B10 protein using HSD17B10 antibody)
IHC (Immunohiostchemistry) (Immunohistochemical analysis of HSD17B10 protein in paraffin embedded Human liver tissue using HSD17B10 antibody)
WB (Western Blot) (Western Blot analysis of HEK293T cell lysates (5 ug) transfected with either recombinant HSD17B10 protein (Right) or empty vector (Left) detected with HSD17B10 antibody)
Application Data (Figure-1: Cell surface staining of PHA stimulated PBMC. Green represents isotype control, red represents Anti-CD137 (AAA78439). 1 ug antibody was used. Goat anti mouse PE was used as secondary antibody.)
IHC (Immunohistochemisry) (Figure-3: Immunohistochemical analysis of CD137. Anti-CD137 (Clone: ABM3D3.2E8) was used in Human Tonsil tissue at 2 ug/ml.)
IHC (Immunohiostchemistry) (Figure-2: Immunohistochemical analysis of CD137. Anti-CD137 (Clone: ABM3D3.2E8) was used in Human Brain tissue at 2 ug/ml.)
WB (Western Blot) (Figure-1: Western Blot analysis of CD137. Anti- CD137 (Clone: ABM3D3.2E8) was tested at 4 ug/ml on Jurkat, HepG2 and Molt-4.)
IHC (Immunohistochemisry) (Fig: 3 Immunohistochemical analysis of UchL1 in human Kidney tissue using UchL1 antibody (Clone: 31A3) at 10 ug/ml.)
IHC (Immunohiostchemistry) (Fig: 2 Immunohistochemical analysis of UchL1 in human Brain using UchL1 antibody (Clone: 31A3) at 1: 500 dilution.)
WB (Western Blot) (Fig: 1 Western blot analysis analysis of UchL1. Anti-UchL1 antibody (Clone: 31A3) was used at 1 ug/ml in 1) human, 2) mouse and 3) rat brain lysate.)
WB (Western Blot) (Western blot analysis of PDL2. Anti-PDL2 antibody (Clone: ABM3D6.1G2)was tested at 0.01 ug/ml on (1) Recombinant protein and 4 ug/ml on (2) U87, (3) Raji, (4) THP1 and (5) RAW Lysates.)
IHC (Immunohistochemistry) (Immunohistochemical analysis of PDL2 in Hepatocellular carcinoma tissue using PDL2 antibody at 5 ug/ml.)
IHC (Immunohiostchemistry) (Fig: 2 Immunohistochemical analysis of CD45RO in human tonsil using CD45RO antibody (Clone: C45.1) at 1:500 dilution.)
FCM/FACS (Flow Cytometry) (Fig.1: Cell Surface flow analysis of hCD45RO in PBMC (Lymphocytes gated) using 0.5 ug antibody per10^6 cells. Green represents isotype control; red represents anti-hCD45RO antibody (10-7509). Goat anti-mouse PE conjugated secondary antibody was used.)
WB (Western Blot) (Figure-2: Western Blot analysis of SARS-CoV-2 Spike RBD Antibody: Anti- SARS-CoV-2 Spike RBD Antibody (Clone: ABM1H9.1E6) was used at 0.5ug/ml on SARS-CoV-2 Spike RBD Recombinant protein.)
WB (Western Blot) (Figure-1: Western Blot analysis of SARS-CoV-2 Spike RBD Antibody: Anti- SARS-CoV-2 Spike RBD Antibody (Clone: ABM1H9.1E6) was used at 0.5ug/ml on mammalian expressed full length spike S1 (21-1008) protein.)
ELISA (Figure-2: An indirect ELISA is carried out by coating Protein A in in serial dilution from 05 ng to 0.078ng and using 100 ng of purified ABM2A4.1E3 monoclonal antibody . Peroxidase conjugated Goat-Anti mouse antibody was used at 1:5000 dilution.)
WB (Western Blot) (Figure-1: Western blot analysis of Protein A. Anti-Protein A antibody (Clone: ABM2A4.1E3) was used at 0.1 ug/ml on Recombinant protein.)
Application Data (PMA and ionomycin stimulated human peripheral blood lymphocytes were stained with Mouse Anti-Human CD3-PE Followed by intracellular staining with Mouse Anti0Human IFN-γ-FITC (AAA78611))
WB (Western Blot) (Western strip blots of HeLa cell crude extracts with two different preparations of CD107a / LAMP1 antibody in strips 17 and 18. Both preparations bind to a diffuse band running at between ~90kDa and ~120kDa as expected, and show no appreciably cross reactivity with any other protein.)
ICC (Immunocytochemistry) (HeLa cells staining with CD107a / LAMP1 antibody (green), and counterstained with chicken polyclonal antibody to Lamin A/C (red) and DNA (blue). The CD107a / LAMP1 antibody antibody reveals strong cytoplasmic staining of lysosomes and early endosomes, while the Lamin A/C antibody binds to the nuclear lamina. Since both DNA (blue) and Lamin A/C (red) are associated with the nuclear compartment, this region appears crimson in this image.)
IHC (Immunohiostchemistry) (Anti-LAMP1 / CD107a antibody IHC staining of human brain, cerebellum. Immunohistochemistry of formalin-fixed, paraffin-embedded tissue after heat-induced antigen retrieval. Antibody dilution 1:50.)
IHC (Immunohistochemistry) (Anti-LAMP1 / CD107a antibody IHC staining of human small intestine. Immunohistochemistry of formalin-fixed, paraffin-embedded tissue after heat-induced antigen retrieval.)
IP (Immunoprecipitation) (Immunoprecipitation(IP) of SERPINA1 by using monoclonal anti-SERPINA1 antibodies (Negative control: IP without adding anti-SERPINA1 antibody.). For each experiment, 500ul of DDK tagged SERPINA1 overexpression lysates (at 1:5 dilution with HEK293T lysate), 2 ug of anti-SERPINA1 antibody and 20ul (0.1 mg) of goat anti-mouse conjugated magnetic beads were mixed and incubated overnight. After extensive wash to remove any non-specific binding, the immuno-precipitated products were analyzed with rabbit anti-DDK polyclonal antibody.)
WB (Western Blot) (HEK293T cells were transfected with the pCMV6-ENTRY control (Left lane) or pCMV6-ENTRY SERPINA1 (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-SERPINA1.)
WB (Western Blot) (Western blot of extracts (35 ug) from 9 different cell lines by using anti-SERPINA1 monoclonal antibody.)
IHC (Immunohistochemistry) (Anti-SERPINA1 / Alpha 1 Antitrypsin antibody IHC staining of human liver. Immunohistochemistry of formalin-fixed, paraffin-embedded tissue after heat-induced antigen retrieval. Antibody concentration 10 ug/ml.)
WB (Western Blot) (HEK293T cells were transfected with the pCMV6-ENTRY control (Left lane) or pCMV6-ENTRY CD163 (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-CD163.)
WB (Western Blot) (Western blot of extracts (35 ug) from 9 different cell lines by using anti-CD163 monoclonal antibody (HepG2: human; HeLa: human; SVT2: mouse; A549: human; COS7: monkey; Jurkat: human; MDCK: canine; PC12: rat; MCF7: human).)
IF (Immunofluorescence) (Anti-CD163 mouse monoclonal antibody immunofluorescent staining of COS7 cells transiently transfected by pCMV6-ENTRY CD163.)
IHC (Immunohistochemistry) (Anti-CD163 antibody IHC staining of human liver. Immunohistochemistry of formalin-fixed, paraffin-embedded tissue after heat-induced antigen retrieval. Antibody concentration 10 ug/ml.)
WB (Western Blot) (HEK293T cells were transfected with the pCMV6-ENTRY control (Left lane) or pCMV6-ENTRY MAGEA3 (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-MAGEA3.)
IHC (Immunohistochemistry) (Anti-MAGEA3 antibody IHC staining of human testis. Immunohistochemistry of formalin-fixed, paraffin-embedded tissue after heat-induced antigen retrieval. Antibody concentration 10 ug/ml.)
FCM/FACS (Flow Cytometry) (Flow cytometry of Jurkat cells, using anti-ALDH1L1 antibody (Red), compared to a nonspecific negative control antibody (Blue).)
WB (Western Blot) (Western blot of extracts (35 ug) from 9 different cell lines by using anti-ALDH1L1 monoclonal antibody.)
WB (Western Blot) (HEK293T cells were transfected with the pCMV6-ENTRY control (Left lane) or pCMV6-ENTRY ALDH1L1 (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-ALDH1L1.)
WB (Western Blot) (Western strip blots of HeLa cell crude extracts stained with anti LAMP1 antibody CD107a / LAMP1 antibody in strip 9. Lane 10 shows staining another LAMP1 antibody. Both antibodies bind to a diffuse band running at between ~90 and ~120kDa as expected, and show no appreciably cross reactivity with any other protein.)
ICC (Immunocytochemistry) (HeLa cells staining with CD107a / LAMP1 antibody (red), and counterstained with chicken polyclonal antibody to Vimentin (green) and DNA (blue). The CD107a / LAMP1 antibody antibody reveals strong punctate cytoplasmic staining corresponding to lysosomes and late endosomes, while the Vimentin antibody reveals cytoplasmic intermediate filaments.)
IHC (Immunohiostchemistry) (Anti-LAMP1 / CD107a antibody IHC staining of human small intestine. Immunohistochemistry of formalin-fixed, paraffin-embedded tissue after heat-induced antigen retrieval.)
IHC (Immunohistochemistry) (Anti-LAMP1 / CD107a antibody IHC staining of human brain, cerebellum. Immunohistochemistry of formalin-fixed, paraffin-embedded tissue after heat-induced antigen retrieval. Antibody concentration 10 ug/ml.)
Standard Curve (Sample) (Representative Standard Curve using mouse monoclonal anti-CD44 (CM0241) for ELISA capture of human recombinant CD44 extracellular region with His-tag. Capture was detected by using an anti-His-tag antibody followed by appropriate secondary antibody conjugated to HRP.)
ICC (Immunocytochemistry) (Immunocytochemical labeling of CD44 in paraformaldehyde fixed human MeWo cells. The cells were labeled with mouse monoclonal anti-CD44 (clone M024). The antibody was detected using goat anti-mouse DyLight 594.)
WB (Western Blot) (Western blot analysis of human A549 (lane 1), MDA-MB-231 (lane 2), and MeWo (lane 3) cell lysates, as well as human breast (lane 4), lung (lane 5), skin (lane 6), and brain (lane 7) tissue lysates. The blot was probed with mouse monoclonal anti-CD44 (CM0241) at 1:2000.)
ICC (Immunocytochemistry) (Immunocytochemical labeling of CD63 in paraformaldehyde fixed human MeWo melanoma cells. The cells were labeled with mouse monoclonal CD63 (CM0401). The antibody was detected using goat anti-mouse Ig DyLight 594.)
WB (Western Blot) (Western blot of native human cell lyastes: MeWo (lane 1), and MeWo treated with PNGase F (lane 2), and A549 (lane 3), and A549 treated with PNGase F (lane 4). The blot was probed with mouse monoclonal CD63 (CM0401) at 1:100.)
Standard Curve (Sample) (Representative Standard Curve using mouse monoclonal anti-His (C-terminal) Tag antibody (HM0501) for ELISA capture of human recombinant CD46 extracellular region with a C-terminal His-tag. Captured protein was detected using anti-CD46 antibody (CM0371) antibody followed by appropriate secondary antibody HRP conjugate.)
ICC (Immunocytochemistry) (Immunocytochemical labeling of Axl recombinant protein with C-terminal His Tag bound to THP1 aldehyde fixed cells. The cells were labeled with mouse monoclonal anti-His (C-terminal) Tag antibody (HM0501). The antibody was detected using goat anti-mouse DyLight 594.)
WB (Western Blot) (Western blot of human recombinant DDR1 protein with C-terminal His Tag. The blot was probed with mouse monoclonal anti-His (Cterminal) Tag (HM0501) at 1:2000 (lane 1), 1:4000 (lane 2), and 1:8000 (lane 3).)
Application Data (Binding curve of anti-CD27 antibody LG.3A10 to mouse CD27-Fc fusion protein ELISA Plate coated with mouse CD27-Fc fusion protein (Pr00160-1.9) at a concentration of 5 ug/ml. A 3-fold serial dilution from 10,000 to 0.1 ng/ml was performed using. For detection, a 1:4000 dilution of HRP-labelled goat anti-rabbit antibody (Bio-Rad) was used.)
IF (Immunofluorescence) (Immunofluorescence staining of fixed mouse splenocytes with anti-CD27 antibody LG.3A10 Immunofluorescence analysis of paraformaldehyde fixed mouse (Mus musculus) splenocytes on Shi-fix coverslips, permeabilized with 0.15% Triton stained with the chimeric rabbit version of LG.3A10 at 10 ug/ml for 1h followed by Alexa Fluor 488 secondary antibody (1 ug/ml), showing membrane and some cytoplasmic staining in a subset of cells. The nuclear stain is DAPI (blue). Panels show from left-right, top-bottom, DAPI, merged channels and an isotype control. The isotype control was stained with an anti-Fluorescein antibody followed by Alexa Fluor 488 secondary antibody.)
IF (Immunofluorescence) (Immunofluorescence staining of fixed RAW264.7 cells with anti-CD86 antibody PO.3 (B467) Immunofluorescence analysis of paraformaldehyde fixed RAW264.7 cells on Shi-fix coverslips stained with the chimeric rabbit IgG version of PO.3 at 10ug/ml for 1h followed by Alexa Fluor 488 secondary antibody (2ug/ml), showing membrane staining. The nuclear stain is DAPI (blue). Panels show from left-right, top-bottom DAPI, merged channels and an isotype control. The isotype control was an unknown specificity antibody followed by staining with Alexa Fluor 488 secondary antibody.)
FCM/FACS (Flow Cytometry) (Flow cytometry using the Anti-CD171 antibody L1-14.10 (AAA72139). Paraformaldehyde fixed HeLa cells were stained with anti-unknown specificity antibody or the mouse IgG1 version of L1-14.10 at a dilution of 1:100 for 1h at RT. After washing, the bound antibody was detected using a goat anti-mouse IgG AlexaFluor 488 antibody at a dilution of 1:1000 and cells analyzed using a FACSCanto flow-cytometer.)
WB (Western Blot) (Western Blot using anti-CD171 antibody L1-14.10 (AAA72139). HeLa(A) (0.03ug/ml), Kelly(B) cells (0.01ug/ml), human brain cerebellum(C) (0.003ug/ml) and cerebral cortex(D) (0.01ug/ml) tissue lysate (35ug protein in RIPA buffer) was resolved on an SDS PAGE gel and blots probed with the chimeric mouse IgG version of L1-14.10 before detection using an anti-mouse secondary antibody. A primary incubation of 1h was used and protein was detected by chemiluminescence.)
IF (Immunofluorescence) (Immunofluorescence staining of HeLa cells using anti-CD171 (AAA72139) L1-14.10 Immunofluorescence analysis of paraformaldehyde fixed HeLa cells stained with the chimeric mouse IgG version of L1-14.10 at 10ug/ml followed by Alexa Fluor 488 secondary antibody (2ug/ml), showing cytoplasmic staining. The nuclear stain is DAPI (blue). Panels show from left-right, top-bottom DAPI, merged channels and an isotype control. The isotype control was stained with anti-unknown antibody followed by Alexa Fluor 488 secondary antibody.)
WB (Western Blot) (Western Blot using anti-CD171 antibody L1-14.10 (AAA72139). HeLa(A) (0.03ug/ml), Kelly(B) cells (0.01ug/ml), human brain cerebellum(C) (0.003ug/ml) and cerebral cortex(D) (0.01ug/ml) tissue lysate (35ug protein in RIPA buffer) was resolved on an SDS PAGE gel and blots probed with the chimeric mouse IgG version of L1-14.10 before detection using an anti-mouse secondary antibody. A primary incubation of 1h was used and protein was detected by chemiluminescence.)
FCM/FACS (Flow Cytometry) (Flow cytometry using the Anti-CD53 antibody HD77 . Paraformaldehyde fixed Daudi cells were stained with anti-unknown specificity antibody or the rabbit IgG version of HD77 at a dilution of 1:100 for 1h at RT. After washing, the bound antibody was detected using a goat anti-rabbit IgG AlexaFluor 488 antibody at a dilution of 1:1000 and cells analyzed using a FACSCanto flow-cytometer.)
IF (Immunofluorescence) (Immunofluorescence staining of fixed Daudi cells with anti-CD53 antibody HD77 Immunofluorescence analysis of paraformaldehyde fixed Daudi cells on Shi-fix coverslips stained with the chimeric rabbit IgG version HD77 at 10ug/ml for 1h followed by Alexa Fluor 488 secondary antibody (2ug/ml), showing membrane staining. The nuclear stain is DAPI (blue). Panels show from left-right, top-bottom DAPI, merged channels and an isotype control. The isotype control was an unknown specificity antibody followed by staining with Alexa Fluor 488 secondary antibody.)
WB (Western Blot) (Western Blot using anti-CD53 antibody HD77 Human lymph node (A), human thymus (B) and human spleen (C) tissue lysates (35ug protein in RIPA buffer) were resolved on a SDS PAGE gel and blots were probed with the chimeric rabbit version of HD77 at 0.1ug/ml, 0.3ug/ml and 0.5ug/ml, respectively, before detection using an anti-rabbit secondary antibody. A primary incubation of 1h was used and protein was detected by chemiluminescence.)
IF (Immunofluorescence) (Immunofluorescence staining of fixed Daudi cells with anti-CD53 antibody HD77 Immunofluorescence analysis of paraformaldehyde fixed Daudi cells on Shi-fix coverslips stained with the chimeric rabbit IgG version HD77 at 10ug/ml for 1h followed by Alexa Fluor 488 secondary antibody (2ug/ml), showing membrane staining. The nuclear stain is DAPI (blue). Panels show from left-right, top-bottom DAPI, merged channels and an isotype control. The isotype control was an unknown specificity antibody followed by staining with Alexa Fluor 488 secondary antibody.)
FCM/FACS (Flow Cytometry) (Flow cytometry using the anti-CCR5 (phosphoserine 349) antibody E11/19 (AAA72175). U937 cells were fixed using 2% PFA and stained with anti-unknown specificity antibody or the rabbit IgG1 version of E11/19 (, blue line) at a dilution of 1:100 for 1h at RT. After washing, the bound antibody was detected using a goat anti-rabbit IgG AlexaFluor 488 antibody at a dilution of 1:1000 and cells analyzed using a FACSCanto flow-cytometer.)
IF (Immunofluorescence) (Immunofluorescence staining of fixed U937 cells with anti-CCR5 (phosphoserine 337) antibody V14/2 (AAA72175) Immunofluorescence analysis of paraformaldehyde fixed U937 cells on Shi-fix coverslips stained with the chimeric rabbit IgG version of V14/2 () at 10ug/ml for 1h followed by Alexa Fluor 488 secondary antibody (2ug/ml), showing membrane staining. The nuclear stain is DAPI (blue). Panels show from left-right, top-bottom , DAPI, merged channels and an isotype control. The isotype control was an unknown specificity antibody followed by staining with Alexa Fluor 488 secondary antibody.)
WB (Western Blot) (Western Blot using anti-CCR5 (phosphoserine 337) antibody V14/2 (AAA72175) K562 cell lysate (35ug protein in RIPA buffer) was resolved on a SDS PAGE gel and blots were probed with the chimeric rabbit version of V14/2 () at 2ug/ml before detection using an anti-rabbit secondary antibody. A primary incubation of 1h was used and protein was detected by chemiluminescence.)
WB (Western Blot) ( Western Blot using anti-HLA class II histocompatibility antigen DR antibody F3.3 Human spleen (A), human tonsil (B) and Daudi cell lysate (C) samples (35ug protein in RIPA buffer) were resolved on a 10% SDS PAGE gel and blots probed with the chimeric rabbit version of F3.3 at 0.01 ug/ml before detection using an anti-rabbit secondary antibody. A primary incubation of 1h was used and protein was detected by chemiluminescence. The expected band size for HLA II DR is ~30 kDa, depending upon the exact DR isoform expressed (c.f. Klitz et al, PMID: 12974796). successfully detected human HLA class II histocompatibility antigen DR in human spleen and tonsil lysate as well as Daudi cell lysate.)
FCM/FACS (Flow Cytometry) ( Flow-cytometry using the anti-HLA II DR antibody F3.3 Daudi cells were stained with unimmunized rabbit IgG antibody (black line) or the rabbit-chimeric version of F3.3 at a concentration of 10 ug/ml for 30 mins at RT. After washing, bound antibody was detected using anti-rabbit IgG JK (FITC-conjugate) antibody (129936) at 2 ug/ml and cells analyzed on a FACSCanto flow-cytometer.)
FCM/FACS (Flow Cytometry) ( Flow-cytometry using anti-HLA class II antibody F3.3 Human leukocytes were stained with an isotype control or the rabbit-chimeric version of F3.3 at a concentration of 1 ug/ml for 30 mins at RT. After washing, bound antibody was detected using a AF488 conjugated donkey anti-rabbit antibody and cells analysed on a FACSCanto flow-cytometer.)
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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