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.
ICC (Immunocytochemistry) (ICC staining pro Caspase 7 in HepG2 cells (green). The nuclear counter stain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.)
ICC (Immunocytochemistry) (ICC staining pro Caspase 7 in Hela cells (green). The nuclear counter stain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.)
IHC (Immunohistochemisry) (Immunohistochemical analysis of paraffin-embedded human kidney tissue using anti-pro Caspase 7 antibody. Counter stained with hematoxylin.)
IHC (Immunohiostchemistry) (Immunohistochemical analysis of paraffin-embedded human liver tissue using anti-pro Caspase 7 antibody. Counter stained with hematoxylin.)
WB (Western Blot) (Western blot analysis of pro Caspase 7 on human lung lysates using anti-pro Caspase 7 antibody at 1/1, 000 dilution.)
FCM/FACS (Flow Cytometry) (Flow cytometric analysis of Hela cells with MuRF1 antibody at 1/100 dilution (green) compared with an unlabelled control (cells without incubation with primary antibody; red).)
ICC (Immunocytochemistry) (ICC staining MuRF1 (green) and Actin filaments (red) in Hela cells. The nuclear counter stain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.)
IHC (Immunohiostchemistry) (Immunohistochemical analysis of paraffin-embedded huamn muscle tissues using anti-MuRF1 antibody. Counter stained with hematoxylin.)
IHC (Immunohistochemistry) (Immunohistochemical analysis of paraffin-embedded human rectum cancer tissues using anti-MuRF1 antibody. Counter stained with hematoxylin.)
FCM/FACS (Flow Cytometry) (Flow cytometric analysis of Hela cells with PCDH9 antibody at 1/100 dilution (green) compared with an unlabelled control (cells without incubation with primary antibody; red).)
ICC (Immunocytochemistry) (ICC staining PCDH9 (green) and Actin filaments (red) in Hela cells. The nuclear counter stain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.)
WB (Western Blot) (Western blot analysis of PCDH9 on C6 cell lysate using anti-PCDH9 antibody at 1/1, 000 dilution.)
WB (Western Blot) (Western blot analysis of PCDH9 on HEK293 (1) and PCDH9-hIgGFc transfected HEK293 (2) cell lysate using anti-PCDH9 antibody at 1/1, 000 dilution.)
WB (Western Blot) (Western blot analysis of PCDH9 on human PCDH9 recombinant protein using anti-PCDH9 antibody at 1/1, 000 dilution.)
IHC (Immunohistochemistry) (Immunohistochemical analysis of paraffin-embedded human colon cancer tissue using anti-EpCAM antibody. Counter stained with hematoxylin.)
IHC (Immunohistochemistry) (Immunohistochemical analysis of paraffin-embedded human colon tissue using anti-EpCAM antibody. Counter stained with hematoxylin.)
IHC (Immunohistochemisry) (Immunohistochemical analysis of paraffin-embedded human liver tissue using anti-EpCAM antibody. Counter stained with hematoxylin.)
IHC (Immunohiostchemistry) (Immunohistochemical analysis of paraffin-embedded human tonsil tissue using anti-EpCAM antibody. Counter stained with hematoxylin.)
WB (Western Blot) (Western blot analysis of EpCAM on different lysates using anti-EpCAM antibody at 1/1, 000 dilution. Positive control: Lane 1: HCT116 Lane 2: SW480)
FCM/FACS (Flow Cytometry) (Flow cytometric analysis of Hela cells with Tuberin antibody at 1/50 dilution (red) compared with an unlabelled control (cells without incubation with primary antibody; black). Alexa Fluor 488-conjugated goat anti rabbit IgG was used as the secondary antibody.)
IHC (Immunohiostchemistry) (Immunohistochemical analysis of paraffin-embedded mouse placenta tissue using anti-Tuberin antibody. Counter stained with hematoxylin.)
WB (Western Blot) (Western blot analysis of Tuberin on Jurkat cell lysates using anti-Tuberin antibody at 1/1, 000 dilution.)
IHC (Immunohistochemistry) (Immunohistochemical analysis of paraffin-embedded mouse kidney tissue using anti-Histone H4 (tri methyl K20) antibody. Counter stained with hematoxylin.)
IHC (Immunohistochemistry) (Immunohistochemical analysis of paraffin-embedded mouse colon tissue using anti-Histone H4 (tri methyl K20) antibody. Counter stained with hematoxylin.)
IHC (Immunohistochemisry) (Immunohistochemical analysis of paraffin-embedded mouse liver tissue using anti-Histone H4 (tri methyl K20) antibody. Counter stained with hematoxylin.)
IHC (Immunohiostchemistry) (Immunohistochemical analysis of paraffin-embedded human kidney tissue using anti-Histone H4 (tri methyl K20) antibody. Counter stained with hematoxylin.)
IHC (Immunohistochemistry) (Immunohistochemical analysis of paraffin-embedded human liver tissue using anti-Histone H4 (tri methyl K20) antibody. Counter stained with hematoxylin.)
IHC (Immunohistochemistry) (Immunohistochemical analysis of paraffin-embedded mouse brain tissue using anti-ULK1 antibody. Counter stained with hematoxylin.)
IHC (Immunohistochemistry) (Immunohistochemical analysis of paraffin-embedded human colon cancer tissue using anti-ULK1 antibody. Counter stained with hematoxylin.)
IHC (Immunohistochemisry) (Immunohistochemical analysis of paraffin-embedded rat skeleton muscle tissue using anti-ULK1 antibody. Counter stained with hematoxylin.)
IHC (Immunohiostchemistry) (Immunohistochemical analysis of paraffin-embedded human spleen tissue using anti-ULK1 antibody. Counter stained with hematoxylin.)
WB (Western Blot) (Western blot analysis of ULK1 on different cell lysate using anti-ULK1 antibody at 1/1, 000 dilution. Positive control�� Lane1: MCF-7 Lane2: Mouse spleen Lane3: SH-SY5Y)
FCM/FACS (Flow Cytometry) (Flow cytometric analysis of Hela cells with USP22 antibody at 1/100 dilution (red) compared with an unlabelled control (cells without incubation with primary antibody; black). Alexa Fluor 488-conjugated goat anti rabbit IgG was used as the secondary antibody.)
ICC (Immunocytochemistry) (ICC staining USP22 in SH-SY5Y cells (green). The nuclear counter stain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.)
ICC (Immunocytochemistry) (ICC staining USP22 in LOVO cells (green). The nuclear counter stain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.)
ICC (Immunocytochemistry) (ICC staining USP22 in Hela cells (green). The nuclear counter stain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.)
WB (Western Blot) (Western blot analysis of USP22 on Hela (1) and HepG2 (2) cell lysate using anti-USP22 antibody at 1/500 dilution.)
FCM/FACS (Flow Cytometry) (Flow cytometric analysis of Hela cells with ADAM17 antibody at 1/50 dilution (red) compared with an unlabelled control (cells without incubation with primary antibody; black). Alexa Fluor 488-conjugated goat anti rabbit IgG was used as the secondary antibody.)
ICC (Immunocytochemistry) (ICC staining ADAM17 in SW480 cells (red). The nuclear counter stain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.)
ICC (Immunocytochemistry) (ICC staining ADAM17 in SKOV-3 cells (red). The nuclear counter stain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.)
ICC (Immunocytochemistry) (ICC staining ADAM17 in HepG2 cells (red). The nuclear counter stain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.)
WB (Western Blot) (Western blot analysis of ADAM17 on Jurkat cells lysates using anti-ADAM17 antibody at 1/1, 000 dilution.)
ICC (Immunocytochemistry) (ICC staining Chromogranin A in PC-3M cells (red). The nuclear counter stain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.)
IHC (Immunohiostchemistry) (Immunohistochemical analysis of paraffin-embedded human pancreas tissue using anti-Chromogranin A antibody. Counter stained with hematoxylin.)
WB (Western Blot) (Western blot analysis of Chromogranin A on PC-12 cells lysates using anti-Chromogranin A antibody at 1/1, 000 dilution.)
IHC (Immunohistochemisry) (IHC of paraffin-embedded human breast cancer using anti- PPP1CA diluted 1/500-1/1000.)
ICC (Immunocytochemistry) (Immunocytochemistry stain of Hela using PPP1CA antibody (1:300).)
WB (Western Blot) (Western blot detection of PPP1CA in MCF7, K562,Hela,HEPG2 &Jurkat Whole cell lysates using PPP1CA antibody (1:1000 diluted).Predicted band size: 38KDaObserved band size: 38KDa)
ICC (Immunocytochemistry) (Immunocytochemistry of Raf1 (green) in MCF-7 using Raf1 antibody at dilution 1/20, and DAPI(blue))
WB (Western Blot) (Western blot detection of Raf1 in C6,3T3,Hela cell lysates using Raf1 Rabbit mAb(1:1000 diluted).Predicted band size:73kDa.Observed band size:73kDa.)
ICC (Immunocytochemistry) (Immunocytochemistry of TRIM56(green) in Hela cells using TRIM56 Rabbit mAb at dilution 1/50, and DAPI(blue))
WB (Western Blot) (Western blot detection of TRIM56 in Hela cell lysates using TRIM56 Rabbit mAb(1:1000 diluted).Predicted band size:82kDa.Observed band size:82kDa.)
ICC (Immunocytochemistry) (Immunocytochemistry analysis of PBR/TSPO (green) in Hela using PBR/TSPO antibody,and DAPI(blue))
IHC (Immunohiostchemistry) (Immunohistochemistry analysis of paraffin-embedded Human breast cancer using PBR antibody.High-pressure and temperature Sodium Citrate pH 6.0 was used for antigen retrieval.)
WB (Western Blot) (Western blot analysis of PBR/TSPO in 3T3, Hela lysates using PBR antibody)
IP (Immunoprecipitation) (Immunoprecipitating PIK3CB in K562 whole cell lysateLane 1: Rabbit control IgG instead of in K562 whole cell lysate. For western blotting,a HRP-conjugated Protein G antibody was used as the secondary antibody (1/2000)Lane 2: K562 whole cell lysate?500ug?Lane 3: K562 whole cell lysate (10ug))
WB (Western Blot) (Western BlotPositive WB detected in: Hela whole cell lysate, K562 whole cell lysateAll lanes: PIK3CB antibody at 1:1500SecondaryGoat polyclonal to rabbit IgG at 1/50000 dilutionPredicted band size: 123 kDaObserved band size: 110 kDa)
IHC (Immunohiostchemistry) (IHC image diluted at 1:100 and staining in paraffin-embedded human kidney tissue performed on a Leica BondTM system. After dewaxing and hydration, antigen retrieval was mediated by high pressure in a citrate buffer (pH 6.0). Section was blocked with 10% normal goat serum 30min at RT. Then primary antibody (1% BSA) was incubated at 4 degree C overnight. The primary is detected by a Goat anti-rabbit IgG polymer labeled by HRP and visualized using 0.05% DAB.)
WB (Western Blot) (Western BlotPositive WB detected in: 293T whole cell lysate, U-251 whole cell lysate, U-87 whole cell lysateAll lanes: Osteopontin Antibody at 1:1000SecondaryGoat polyclonal to rabbit IgG at 1/50000 dilutionPredicted band size: 36, 34, 33, 34, 34 kDaObserved band size: 36 kDa)
WB (Western Blot) (HeLa cells were subjected to SDS PAGE followed by western blot with AAA249053 (PARP1 Antibody) at dilution of 1:20000)
IF (Immunofluorescence) (Immunofluorescent analysis of HeLa cells using AAA249053 (PARP1 antibody) at dilution of 1:100 and Alexa Fluor 488-conjugated Goat Anti-Mouse IgG (H+L))
IHC (Immunohistochemistry) (Immunohistochemistry of paraffin-embedded human breast cancer using AAA249053 (PARP1 antibody) at dilution of 1:600)
WB (Western Blot) (HeLa cells were subjected to SDS PAGE followed by western blot with AAA247976 (LMNB1 antibody) at dilution of 1:10000)
IP (Immunoprecipitation) (IP Result of anti-Lamin B1 (IP: AAA247976, 4ug; Detection: AAA247976 1:40000) with HeLa cells lysate 2000ug.)
IHC (Immunohistochemistry) (Immunohistochemistry of paraffin-embedded human pancreas cancer tissue slide using AAA247976 (Lamin B1 antibody) at dilution of 1:1000)
IHC (Immunohistochemisry) (Immunohistochemical analysis of paraffin-embedded Mouse BrainTissue using PI3 Kinase P85 ? Mouse mAb diluted at 1:200.)
Application Data (Wang. L.. Xiong. Q.. Li. P. et al. The negative charge of the 343 site is essential for maintaining physiological functions of CXCR4. BMC Mol and Cell Biol 22. 8 (2021). )
WB (Western Blot) (Western blot analysis of 1)3T3. 2) Rat LiverTissue with PI3 Kinase P85? Mouse mAb diluted at 1:2.000.)
IHC (Immunohistochemisry) (Immunohistochemical analysis of paraffin-embedded Human Colon Carcinoma Tissue using Gamma Tubulin Mouse mAb diluted at 1:200.)
IHC (Immunohiostchemistry) (Immunohistochemical analysis of paraffin-embedded Human Breast Carcinoma Tissue using Gamma Tubulin Mouse mAb diluted at 1:200.)
WB (Western Blot) (Western Blot analysis of paraffin-embedded JurkatHelaMouse-brainRat-brain using Gamma Tubulin Mouse mAb diluted at 1:1000.)
SDS-PAGE (Various whole cell lysates were separated by 12% SDS-PAGE, and the membrane was blotted with anti-CK7 (ABT436)antibody. The HRP-conjugated Goat anti-M)
FCM/FACS (Flow Cytometry) (Flow cytometric analysis of K562 cells using HXK II Monoclonal Antibody (green) and negative control (purple).)
IHC (Immunohiostchemistry) (Immunohistochemistry analysis of paraffin-embedded esophagus cancer tissues (left) and human lung cancer (right) with DAB staining using HXK II Monoclonal Antibody.)
WB (Western Blot) (Western Blot analysis using HXK II Monoclonal Antibody against Jurkat (1). HeLa (2) and HEK293 (3) cell lysate.)
FCM/FACS (Flow Cytometry) (Flow cytometric analysis of A549 cells using IKK? Monoclonal Antibody (blue) and negative control (red).)
IF (Immunofluorescence) (Immunofluorescence analysis of NIH/3T3 cells using IKK? 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 IKK? Monoclonal Antibody against Raji (1). Jurkat (2). THP-1 (3) and K562 (4) cell lysate.)
FCM/FACS (Flow Cytometry) (Flow cytometric analysis of Hela cells using JAK3 Monoclonal Antibody (blue) and negative control (red).)
IF (Immunofluorescence) (Confocal immunofluorescence analysis of Hela (left) and HepG2 (right) cells using JAK3 Monoclonal Antibody (green). Red: Actin filaments have been labeled with DY-554 phalloidin. Blue: DRAQ5 fluorescent DNA dye.)
WB (Western Blot) (Western Blot analysis using JAK3 Monoclonal Antibody against Jurkat cell lysate (1).)
IF (Immunofluorescence) (Immunofluorescence analysis of Hela cells using JMJD1A 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 JMJD1A Monoclonal Antibody against HeLa (1) and HepG2 (2) cell lysate.)
IF (Immunofluorescence) (Confocal immunofluorescence analysis of methanol-fixed HEK293 cells trasfected with LCN1-hIgGFc using Lipocalin-1 Monoclonal Antibody (green). showing membrane localization. Blue: DRAQ5 fluorescent DNA dye.)
IHC (Immunohiostchemistry) (Immunohistochemistry analysis of paraffin-embedded human Prostate tissues with AEC staining using Lipocalin-1 Monoclonal Antibody.)
WB (Western Blot) (Western Blot analysis using Lipocalin-1 Monoclonal Antibody against HEK293 (1) and LCN1-hIgGFc transfected HEK293 cell lysate (2).)
FCM/FACS (Flow Cytometry) (Flow cytometric analysis of Hela cells using MEK-2 Monoclonal Antibody (green) and negative control (purple).)
IF (Immunofluorescence) (Immunofluorescence analysis of Hela cells using MEK-2 Monoclonal Antibody (green). Red: Actin filaments have been labeled with DY-554 phalloidin. Blue: DRAQ5 fluorescent DNA dye.)
WB (Western Blot) (Western Blot analysis using MEK-2 Monoclonal Antibody against PC-12 (1). Jurkat (2). HeLa (3) and NIH/3T3 (4) cell lysate.)
ICC (Immunocytochemistry) (Immunocytochemistry of HeLa cells fixed by Paraformaldehyde and using DR5 mouse mAb diluted 1:100.)
WB (Western Blot) (Western blot detection of DR5 in Mouse kindey.Mouse brain.HCT116 and Hela cell lysates using DR5 mouse mAb (1:500-1:2000 diluted).Predicted band size:40/48KDa.Observed band size:40/48KDa.)
IF (Immunofluorescence) (Immunofluorescent analysis of Hela cells using Ku80 mouse mAb (1:400).)
IP (Immunoprecipitation) (Immunoprecipitation analysis of Hela cell lysates using Ku80 mouse mAb.)
WB (Western Blot) (Western blot detection of Ku80 in COS7.Jurkat.Hela.MCF7 and A549 cell lysates using Ku80 mouse mAb (1:1000 diluted). Predicted band size:86KDa. Observed band size:86KDa.)
IHC (Immunohiostchemistry) (Immunohistochemistry analysis of paraffin-embedded human skeletal muscle tissue showing cytoplasmic localization with DAB staining using Myoglobin Monoclonal Antibody.)
WB (Western Blot) (Western Blot analysis using Myoglobin Monoclonal Antibody against truncated Myoglobin recombinant protein.)
FCM/FACS (Flow Cytometry) (Flow cytometric analysis of Jurkat cells using ETS1 Monoclonal Antibody (green) and negative control (purple).)
IF (Immunofluorescence) (Immunofluorescence analysis of NIH/3T3 cells using ETS1 Monoclonal Antibody (green). Blue: DRAQ5 fluorescent DNA dye.)
IHC (Immunohiostchemistry) (Immunohistochemistry analysis of paraffin-embedded human Colon. Adipocytes tissues with AEC staining using ETS1 Monoclonal Antibody.)
WB (Western Blot) (Western Blot analysis using ETS1 Monoclonal Antibody against Jurkat (1). HepG2 (2) and ETS1-hIgGFc transfected HEK293 (3) cell lysate.)
IHC (Immunohiostchemistry) (Immunohistochemistry analysis of paraffin-embedded human cerebrum tumor (A). endothelium of vessel (B). lymphocyte of thymus(C). showing cytoplasmic localization with DAB staining using Fes Monoclonal Antibody.)
WB (Western Blot) (Western Blot analysis using Fes Monoclonal Antibody against truncated Fes recombinant protein.)
Application Data (Analysis of Protein Array containing more than 19,000 full-length human proteins using Cytokeratin 20 (KRT20) Mouse Monoclonal Antibody (KRT20/1991). Z- and S- Score: The Z-score represents the strength of a signal that a monoclonal antibody (MAb) (in combination with a fluorescently-tagged anti-IgG secondary antibody) produces when binding to a particular protein on the HuProtTM array. Z-scores are described in units of standard deviations (SD's) above the mean value of all signals generated on that array. If targets on HuProtTM are arranged in descending order of the Z-score, the S-score is the difference (also in units of SD's) between the Z-score. S-score therefore represents the relative target specificity of a MAb to its intended target. A MAb is considered to specific to its intended target, if the MAb has an S-score of at least 2.5. For example, if a MAb binds to protein X with a Z-score of 43 and to protein Y with a Z-score of 14, then the S-score for the binding of that MAb to protein X is equal to 29.)
SDS_PAGE (SDS-PAGE Analysis Purified Cytokeratin 20 (KRT20) Mouse Monoclonal Antibody (KRT20/1991). Confirmation of Purity and Integrity of Antibody.)
WB (Western Blot) (Western Blot Analysis of human HT29 Cell lysate using Cytokeratin 20 (KRT20) Mouse Monoclonal Antibody (KRT20/1991).)
IHC (Immunohiostchemistry) (Formalin-fixed, paraffin-embedded human Normal Colon stained with Cytokeratin 20 (KRT20) Mouse Monoclonal Antibody (KRT20/1991).)
IHC (Immunohistochemistry) (Formalin-fixed, paraffin-embedded human Colon Carcinoma stained with Cytokeratin 20 (KRT20) Mouse Monoclonal Antibody (KRT20/1991).)
The purified antibody is conjugated with R-phycoerythrin (PE) under optimum conditions. The conjugate is purified by size-exclusion 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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