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.
WB (Western Blot) (K-562 cells were subjected to SDS PAGE followed by western blot with AAA248080 (SECTM1 Antibody) at dilution of 1:1000)
IHC (Immunohistochemistry) (Immunohistochemistry of paraffin-embedded human colon cancer tissue slide using AAA248080 (SECTM1 Antibody) at dilution of 1:200)
IHC (Immunohistochemistry) (Immunohistochemical analysis of paraffin-embedded mouse lung tissue using anti-Mast Cell Tryptase antibody. Counter stained with hematoxylin.)
IHC (Immunohistochemisry) (Immunohistochemical analysis of paraffin-embedded human lung tissue using anti-Mast Cell Tryptase antibody. Counter stained with hematoxylin.)
IHC (Immunohiostchemistry) (Immunohistochemical analysis of paraffin-embedded human tonsil tissue using anti-Mast Cell Tryptase antibody. Counter stained with hematoxylin.)
WB (Western Blot) (Western blot analysis of Mast Cell Tryptase on human skin lysates using anti-Mast Cell Tryptase antibody at 1/1, 000 dilution.)
FCM/FACS (Flow Cytometry) (Flow cytometric analysis of Daudi cells with FKBP51 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.)
IHC (Immunohistochemistry) (Immunohistochemical analysis of paraffin-embedded rat lung tissue tissue using anti-FKBP51 antibody. Counter stained with hematoxylin.)
IHC (Immunohistochemisry) (Immunohistochemical analysis of paraffin-embedded human kidney tissue using anti-FKBP51 antibody. Counter stained with hematoxylin.)
IHC (Immunohiostchemistry) (Immunohistochemical analysis of paraffin-embedded human tonsil tissue using anti-FKBP51 antibody. Counter stained with hematoxylin.)
WB (Western Blot) (Western blot analysis of FKBP51 on rat kidney tissue and Daudi cell lysate using anti-FKBP51 antibody at 1/500 dilution.)
ICC (Immunocytochemistry) (ICC staining NEDD8 in HepG2 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 breast carcinoma tissue using anti-NEDD8 antibody. Counter stained with hematoxylin.)
IHC (Immunohistochemistry) (Immunohistochemical analysis of paraffin-embedded human lung cancer tissue using anti-NEDD8 antibody. Counter stained with hematoxylin.)
Application Data (Analysis of Protein Array containing more than 19,000 full-length human proteins using APEX Nuclease I Mouse Monoclonal Antibody (CPTC-APEX1-2). 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.)
IHC (Immunohistochemistry) (Formalin-fixed, paraffin-embedded human Prostate Carcinoma stained with APEX Nuclease I Mouse Monoclonal Antibody (CPTC-APEX1-2).)
IF (Immunofluorescence) (Immunofluorescence analysis of Human-breast-cancer tissue. 1.Oct1 Monoclonal Antibody(7G1)(red) was diluted at 1:200(4 degree C.overnight). 2. Cy3 labled Secondary antibody was diluted at 1:300(room temperature. 50min).3. Picture B: DAPI(blue) 10min. Picture A:Target. Picture B: DAPI. Picture C: merge of A+B)
IHC (Immunohiostchemistry) (Immunohistochemical analysis of paraffin-embedded Human-breast-cancer tissue. 1.Oct1 Monoclonal Antibody(7G1) was diluted at 1:200(4 degree C.overnight). 2. Sodium citrate pH 6.0 was used for antibody retrieval(>98 degree C.20min). 3.Secondary antibody was diluted at 1:200(room temperature. 30min). Negative control was used by secondary antibody only.)
WB (Western Blot) (Western blot analysis of 1) Hela. 2) Jurkat. 3) HepG2. diluted at 1:2000 cells nucleus extracted by Minute TM Cytoplasmic and Nuclear Fractionation kit (SC-003.Inventbiotech.MN.USA).)
IHC (Immunohistochemistry) (Immunohistochemical analysis of paraffin-embedded Mouse-liver tissue. 1.Fibronectin Monoclonal Antibody(M9) was diluted at 1:200(4 degree C.overnight). 2. Sodium citrate pH 6.0 was used for antibody retrieval(>98 degree C.20min). 3.Secondary antibody was diluted at 1:200(room temperature. 30min). Negative control was used by secondary antibody only.)
IHC (Immunohistochemistry) (Immunohistochemical analysis of paraffin-embedded Human kidney. 1. Antibody was diluted at 1:100(4 degree overnight). 2. High-pressure and temperature EDTA. pH8.0 was used for antigen retrieval. 3.Secondary antibody was diluted at 1:200(room temperature. 30min).)
IHC (Immunohistochemisry) (Immunohistochemical analysis of paraffin-embedded Human kidney. 1. Antibody was diluted at 1:100(4 degree overnight). 2. High-pressure and temperature EDTA. pH8.0 was used for antigen retrieval. 3.Secondary antibody was diluted at 1:200(room temperature. 30min).)
IHC (Immunohiostchemistry) (Immunohistochemical analysis of paraffin-embedded Human kidney. 1. Antibody was diluted at 1:100(4 degree overnight). 2. High-pressure and temperature EDTA. pH8.0 was used for antigen retrieval. 3.Secondary antibody was diluted at 1:200(room temperature. 30min).)
WB (Western Blot) (Western blot analysis of Hela. diluted at 1:2000.)
IHC (Immunohistochemisry) (Immunohistochemical analysis of paraffin-embedded Human Breast Carcinoma using Acetyl Lysine Monoclonal Antibody.)
IP (Immunoprecipitation) (Immunoprecipitate analysis of A431 whole cell lysate (pretreated with Trichostatin A) by Acetyl Lysine Monoclonal Antibody(10B10) . lane1: Histone H3 (Acetyl Lys9) Polyclonal Antibody Primary Antibody was diluted at 1:1000. lane2:p53 (Acetyl Lys381) Polyclonal Antibody Primary Antibody was diluted at 1:1000. lane3:NF?B-p65 (Acetyl Lys310) Polyclonal AntibodyPrimary Antibody was diluted at 1:1000. Secondary antibody)
WB (Western Blot) (Western blot analysis of 1) Mouse Brain Tissue. 2) Hela. 3) Hela+TSA Treated using Acetyl Lysine Monoclonal Antibody.)
FCM/FACS (Flow Cytometry) (Flow cytometric analysis of EC cells using NGFR p75 Monoclonal Antibody (green) and negative control (purple).)
IF (Immunofluorescence) (Immunofluorescence analysis of EC cells using NGFR p75 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 NGFR p75 Monoclonal Antibody against NGFR-hIgGFc transfected HEK293 cell lysate.)
FCM/FACS (Flow Cytometry) (Flow cytometric analysis of Lovo cells using PDK1 Monoclonal Antibody (green) and negative control (purple).)
IF (Immunofluorescence) (Immunofluorescence analysis of HELA cells using PDK1 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 PDK1 Monoclonal Antibody.)
WB (Western Blot) (Western Blot analysis using PDK1 Monoclonal Antibody against NIH/3T3 (1). HeLa (2). Jurkat (3). HepG2 (4). PC-12 (5). and Cos7 (6) cell lysate.)
WB (Western Blot) (Western Blot analysis using PGC-1? Monoclonal Antibody against HEK293 (1) and PGC-1alpha-hIgGFc transfected HEK293 (2) cell lysate.)
IHC (Immunohiostchemistry) (Immunohistochemistry analysis of paraffin-embedded human ovarian cancer (left) and breast cancer (right) tissues with DAB staining using PMR1 Monoclonal Antibody.)
WB (Western Blot) (Western Blot analysis using PMR1 Monoclonal Antibody against A431 (1). HeLa (2) and HEK293 (3) cell lysate.)
FCM/FACS (Flow Cytometry) (Flow cytometric analysis of HepG2 cells using RBP4 Monoclonal Antibody (green) and negative control (purple).)
IF (Immunofluorescence) (Immunofluorescence analysis of HepG2 cells using RBP4 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 liver cancer tissues (left) and stomach cancer tissues (right) with DAB staining using RBP4 Monoclonal Antibody.)
WB (Western Blot) (Western Blot analysis using RBP4 Monoclonal Antibody against HEK293 (1) and RBP4-hIgGFc transfected HEK293 (2) cell lysate.)
WB (Western Blot) (Western blot detection of IMP3 in MCF7.SKVO3.NTERA2.Jurkat.Hela and K562 cell lysates using IMP3 mouse mAb (1:1000 diluted).Predicted band size:70KDa.Observed band size:70KDa.)
WB (Western Blot) (Western blot detection of OLIG2 in CHO-K1 cell lysate(B)and CHO-K1 transfected by EGFP-OLIG2 fragment(A)cell lysate using OLIG2 mouse mAb (1:1000 diluted).)
ICC (Immunocytochemistry) (Immunocytochemistry staining of HeLa cells fixed with -20? Methanol and using anti-RPA32/RPA2 antibody (dilution 1:200).)
IP (Immunoprecipitation) (Immunoprecipitation analysis of Hela cell lysates using RPA32/RPA2 mouse mAb.)
WB (Western Blot) (Western blot detection of RPA32/RPA2 in MCF7.Hela and HUVEC cell lysates using RPA32/RPA2 mouse mAb (1:2000 diluted).Predicted band size:32KDa.Observed band size:32KDa.Exposure time:20s.)
ICC (Immunocytochemistry) (Immunocytochemistry staining of MDA-MB-468 cells fixed with 4% Paraformaldehyde and using EGFR mouse mAb (dilution 1:200).)
ICC (Immunocytochemistry) (Immunocytochemistry staining of HeLa cells using EGFR mouse mAb (dilution 1:200).)
IP (Immunoprecipitation) (Immunoprecipitation analysis of Hela cell lysates using EGFR mouse mAb.)
WB (Western Blot) (Western blot detection of EGFR in A549.MDA-MB-468 and COS7 cell lysates using EGFR mouse mAb(dilution 1:1000).Predicted band size:134 Kda.Observed band size:175KDa.)
FCM/FACS (Flow Cytometry) (Flow cytometric analysis of HepG2 cells using UBC9 Monoclonal Antibody (green) and negative control (red).)
IF (Immunofluorescence) (Immunofluorescence analysis of HepG2 cells using UBC9 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 prostate tissues with DAB staining using UBC9 Monoclonal Antibody.)
WB (Western Blot) (Western Blot analysis using UBC9 Monoclonal Antibody against HeLa (1). HepG2 (2). and Cos7 (3) cell lysate.)
FCM/FACS (Flow Cytometry) (Flow cytometric analysis of K562 cells stained with TORC1 Monoclonal Antibody (red). followed by FITC-conjugated goat anti-mouse IgG. Blue line histogram represents the isotype control. normal mouse IgG.)
WB (Western Blot) (Western Blot analysis using TORC1 Monoclonal Antibody against HeLa. Jurkat cell lysate.)
IP (Immunoprecipitation) (Immunoprecipitation analysis of Hela cell lysates using PRMT4/CARM1 mouse mAb.)
WB (Western Blot) (Western blot detection of PRMT4/CARM1 in Hela.A431 and K562 cell lysates using PRMT4/CARM1 mouse mAb (1:200-1:500 diluted).Predicted band size:63KDa.Observed band size:63KDa.)
ICC (Immunocytochemistry) (Immunocytochemistry staining of HeLa cells fixed with 4% Paraformaldehyde and using anti-pyruvate dehydrogenase (lipoamide) alpha 1 mouse mAb(dilution 1:100).)
WB (Western Blot) (Western blot detection of pyruvate dehydrogenase (lipoamide) alpha 1 in 293.1299.mEsc and Tc1 cell lysates using pyruvate dehydrogenase (lipoamide) alpha 1 mouse mAb (1:1000 diluted).Predicted band size: 43KDa.Observed band size: 43KDa.)
IHC (Immunohiostchemistry) (Immunohistochemistry analysis of paraffin-embedded rectum cancer tissues (left) and stomach cancer tissues (right) with DAB staining using CD66e Monoclonal Antibody.)
WB (Western Blot) (Western Blot analysis using CD66e Monoclonal Antibody against HEK293 (1) and CEA-hIgGFc transfected HEK293 (2) cell lysate.)
IHC (Immunohiostchemistry) (Immunohistochemistry analysis of paraffin-embedded cervical cancer tissues (left) and tonsil tissues (right) with DAB staining using Cortactin Monoclonal Antibody.)
WB (Western Blot) (Western Blot analysis using Cortactin Monoclonal Antibody against HeLa (1). A431 (2). MCF-7 (3). SR-BR-3 (4). HepG2 (5) and NIH/3T3 (6) cell lysate.)
IHC (Immunohiostchemistry) (Immunohistochemistry analysis of paraffin-embedded human brain tumor tissue. showing nuclear and cytoplasmic localization with DAB staining using Elk1 Monoclonal Antibody.)
WB (Western Blot) (Western Blot analysis using Elk1 Monoclonal Antibody against truncated ELK1 recombinant protein (1) and K562 cell lysate (2).)
IHC (Immunohiostchemistry) (Immunohistochemistry analysis of paraffin-embedded human stomach carcinoma (left) and breast carcinoma (right). showing cytoplasmic localization with DAB staining using Fibulin-5 Monoclonal Antibody.)
WB (Western Blot) (Western Blot analysis using Fibulin-5 Monoclonal Antibody against truncated fibulin5 recombinant protein (1) and HeLa cell lysate (2).)
IF (Immunofluorescence) (Confocal immunofluorescence analysis of PANC-1 cells using FoxP3 Monoclonal Antibody (green). Red: Actin filaments have been labeled with Alexa Fluor-555 phalloidin.)
IHC (Immunohiostchemistry) (Immunohistochemistry analysis of paraffin-embedded human lymphocyto tissue. showing cytoplasmic and nuclear localization with DAB staining using FoxP3 Monoclonal Antibody.)
WB (Western Blot) (Western Blot analysis using FoxP3 Monoclonal Antibody against truncated Foxp3 recombinant (1) and HEK293 cell lysate (2).)
FCM/FACS (Flow Cytometry) (Flow cytometric analysis of K562 cells using GSTP1 Monoclonal Antibody (green) and negative control (purple).)
IF (Immunofluorescence) (Confocal immunofluorescence analysis of HepG2 (left) and L-02 (right) cells using GSTP1 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 prostate tissues with DAB staining using GSTP1 Monoclonal Antibody.)
WB (Western Blot) (Western Blot analysis using GSTP1 Monoclonal Antibody against PC3 cell lysate (1) and human cerebellum tissue lysate (2).)
IHC (Immunohiostchemistry) (Immunohistochemistry analysis of paraffin-embedded human lung cancer (A). recturn(B). prostate (C). colon cancer (D) showing cytoplasmic localization with DAB staining using IGFBP2 Monoclonal Antibody.)
WB (Western Blot) (Western Blot analysis using IGFBP2 Monoclonal Antibody against truncated IGFBP2-His recombinant protein (1) and truncated IGFBP2 (aa40-328)-hIgGFc transfected CHO-K1 cell lysate (2).)
IHC (Immunohiostchemistry) (Immunohistochemistry analysis of paraffin-embedded ovarian cancer tissues using IGF-IR Monoclonal Antibody with DAB staining.)
WB (Western Blot) (Western Blot analysis using IGF-IR Monoclonal Antibody against truncated IGF-IR recombinant protein.)
IF (Immunofluorescence) (Confocal immunofluorescence analysis of HEK293 cells trasfected with full-length ISL1-hIgGFc using Islet-1 Monoclonal Antibody (green). Blue: DRAQ5 fluorescent DNA dye.)
IHC (Immunohiostchemistry) (Immunohistochemistry analysis of paraffin-embedded human lung cancer (left) and cervical carcinoma (right). showing nuclear localization with DAB staining using Islet-1 Monoclonal Antibody.)
WB (Western Blot) (Western Blot analysis using Islet-1 Monoclonal Antibody against full-length ISL1 (aa1-349)-hIgGFc transfected HEK293 cell lysate(1).)
IF (Immunofluorescence) (Immunofluorescence staining of methanol-fixed A431 (left) and Hela (right) cells showing cytoplasmic and membrane localization using JNK3 Monoclonal Antibody.)
WB (Western Blot) (Western Blot analysis using JNK3 Monoclonal Antibody against NIH/3T3 (1) and SKN-SH (2) cell lysate.)
IHC (Immunohiostchemistry) (Immunohistochemistry analysis of paraffin-embedded human brain tissues with DAB staining using KLHL21 Monoclonal Antibody.)
WB (Western Blot) (Western Blot analysis using KLHL21 Monoclonal Antibody against recombinant KLHL21 protein (1).)
IF (Immunofluorescence) (Immunofluorescence analysis of Hela cells using LHX2 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 LHX2 Monoclonal Antibody against human LHX2 (AA: 200-406) recombinant protein.)
IHC (Immunohiostchemistry) (Immunohistochemistry analysis of paraffin-embedded human cervical carcinoma. showing cytoplasmic localization with DAB staining using LysRS Monoclonal Antibody.)
WB (Western Blot) (Western Blot analysis using LysRS Monoclonal Antibody against truncated Trx-LysRS recombinant protein (1). truncated MBP-LysRS (aa90-174) and full length LysRS (aa1-188) transfected CHO-K1 cell lysate (3).)
IF (Immunofluorescence) (Immunofluorescence analysis of Hela cells using Matrilin-1 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 Matrilin-1 Monoclonal Antibody against HEK293 (1) and MATN1-hIgGFc transfected HEK293 (2) cell lysate.)
IHC (Immunohistochemistry) (Immunohistochemical analysis of paraffin-embedded Human-breast tissue. 1.ATG5 Mouse Monoclonal Antibody(3C7) was diluted at 1:200(4 degree C.overnight). 2. Sodium citrate pH 6.0 was used for antibody retrieval(>98 degree C.20min). 3.Secondary antibody was diluted at 1:200(room temperature. 30min). Negative control was used by secondary antibody only.)
IHC (Immunohistochemistry) (Immunohistochemical analysis of paraffin-embedded Human Ovarian Carcinoma Tissue using ATG5 Mouse mAb diluted at 1:200.)
IHC (Immunohistochemisry) (Immunohistochemical analysis of paraffin-embedded Human Breast Carcinoma Tissue using ATG5 Mouse mAb diluted at 1:200.)
Application Data (Deng. Z.. Sun. M.. Wu. J. et al. SIRT1 attenuates sepsis-induced acute kidney injury via Beclin1 deacetylation-mediated autophagy activation. Cell Death Dis 12. 217 (2021). )
WB (Western Blot) (Western blot analysis of Hela Cell Lysate using ATG5 Mouse mAb diluted at 1:10000)
Immunoprecipitation, Immunohistochemistry, Western Blot, Immunocytochemistry, Immunofluorescence
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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