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 (Immunohiostchemistry) (Immunohistochemistry of HIF1 beta in paraffin-embedded Human lung cancer tissue using HIF1 beta Rabbit mAb at dilution 1/50)
WB (Western Blot) (Western blot detection of HIF1 beta in Hela,CHO-K1,C6, Ramos using HIF1 beta Rabbit mAb(1:1000 diluted))
IF (Immunofluorescence) (Immunofluorescence of FH (green) in hela using FH Rabbit mAb at dilution 1/50, and DAPI(blue))
WB (Western Blot) (Western blot detection of FH/Fumarase in CHO-K1,C6,Jurkat cell lysates using FH/Fumarase Rabbit mAb(1:500 diluted).Predicted band size:55kDa.Observed band size:49kDa.)
FCM/FACS (Flow Cytometry) (Flow cytometric analysis of MSCS cells using DDX4 Monoclonal Antibody (green) and negative control (purple).)
IF (Immunofluorescence) (Immunofluorescence analysis of MSCs(left) and NTERA-2 (right) cells using DDX4 Monoclonal Antibody (green). Red: Actin filaments have been labeled with DY-554 phalloidin.)
IHC (Immunohiostchemistry) (Immunohistochemistry analysis of paraffin-embedded human lung cancer (A) and rectal cancer (B). showing cytoplasmic localization with DAB staining using DDX4 Monoclonal Antibody.)
WB (Western Blot) (Western Blot analysis using DDX4 Monoclonal Antibody against DDX4-hIgGFc transfected HEK293 cell lysate.)
IHC (Immunohiostchemistry) (Immunohistochemistry analysis of paraffin-embedded human recturn adenocarcinoma tissue showing cytoplasmic localization with DAB staining using FGF-2 Monoclonal Antibody.)
WB (Western Blot) (Western Blot analysis using FGF-2 Monoclonal Antibody against truncated FGF-2 recombinant protein.)
FCM/FACS (Flow Cytometry) (Flow cytometric analysis of PC-2 cells using AMPK?1 Monoclonal Antibody (green) and negative control (purple).)
IF (Immunofluorescence) (Immunofluorescence analysis of NTERA-2 cells using AMPK?1 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 ovarian cancer (left) and brain tissues (right) with DAB staining using AMPK?1 Monoclonal Antibody.)
WB (Western Blot) (Western Blot analysis using AMPK?1 Monoclonal Antibody against Jurkat (1). HeLa (2). HepG2 (3). MCF-7 (4). Cos7 (5). NIH/3T3 (6). K562 (7). HEK293 (8). and PC-12 (9) cell lysate.)
FCM/FACS (Flow Cytometry) (Flow cytometric analysis of Hela cells using Ku-80 Monoclonal Antibody (green) and negative control (purple).)
IF (Immunofluorescence) (Immunofluorescence analysis of Hela cells using Ku-80 Monoclonal Antibody (green). Red: Actin filaments have been labeled with Alexa Fluor-555 phalloidin.)
IHC (Immunohiostchemistry) (Immunohistochemistry analysis of paraffin-embedded human tonsil tissues (left) and human colon cancer tissues (right) with DAB staining using Ku-80 Monoclonal Antibody.)
WB (Western Blot) (Western Blot analysis using Ku-80 Monoclonal Antibody against HeLa (1). MCF-7 (2). A549 (3) and NIH/3T3 (4) cell lysate.)
IHC (Immunohiostchemistry) (Immunohistochemistry analysis of paraffin-embedded human striated muscle tissues with DAB staining using Lamin A Monoclonal Antibody.)
WB (Western Blot) (Western Blot analysis using Lamin A Monoclonal Antibody against Raw264.7 (1). PC-12 (2). THP-1 (3). A431 (4). MCF-7 (5) and Jurkat (6) cell lysate.)
IP (Immunoprecipitation) (Immunoprecipitation analysis of Hela cell lysates using STAT1 mouse mAb.)
WB (Western Blot) (Western blot detection of STAT1 in Hela.MCF7.COS7.SW480 and A549 cell lysates using STAT1 mouse mAb (1:1000 diluted).Predicted band size:91KDa.Observed band size:91KDa.)
IF (Immunofluorescence) (Immunofluorescent analysis of Hela cells fixed with 4% Paraformaldehyde and using anti-BRG1 mouse mAb (dilution 1:50). DAPI was used to stain nucleus(blue).)
IP (Immunoprecipitation) (Immunoprecipitation analysis of K562 cell lysates using BRG1 mouse mAb (201025).)
WB (Western Blot) (Western blot detection of BRG1 in Hela NE.F9 and K562 cell lysates using BRG1 mouse mAb (1:1000 diluted).Predicted band size:220KDa.Observed band size:220KDa.)
IP (Immunoprecipitation) (Immunoprecipitation analysis of Hela cell lysates using FEN-1 mouse mAb.)
WB (Western Blot) (Western blot detection of FEN-1 in Hela.Jurkat.3T3.C6.CEM and Ramos cell lysates using FEN-1 mouse mAb (1:1000 diluted).Predicted band size:45KDa.Observed band size:45KDa.)
WB (Western Blot) (Western blot detection of FEN-1 in Hela.Hela NE.Jurkat.K562 and 3T3 cell lysates using FEN-1 mouse mAb (1:1000 diluted).Predicted band size:45KDa.Observed band size:45KDa.)
IP (Immunoprecipitation) (Immunoprecipitation analysis of Hela cell lysates using SIRT1 mouse mAb.)
WB (Western Blot) (Western blot detection of SIRT1 in Hela.Jurkat.Ramos.A549 and CEM cell lysates using SIRT1 mouse mAb (1:1000 diluted).Predicted band size:120KDa.Observed band size:120KDa.)
SDS-PAGE (HepG2 whole cell lysates were separated by 10% SDS-PAGE, and the membrane was blotted with anti-Glypican-3(ABT180) 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 13 (ABT057) antibody. The HRP-conjugated Goat anti-M)
WB (Western Blot) (Western blot analysis of 1) Hela Cell Lysate, 2) Mouse Heart Tissue Lysate, 3)Rat Heart Tissue Lysate using GSK 3? Mouse mAb diluted at 1:1000.)
IHC (Immunohistochemistry) (Immunohistochemical analysis of paraffin-embedded Human Lung Carcinoma Tissue using GSK3? Mouse mAb diluted at 1:200.)
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)
IHC (Immunohiostchemistry) (Immunohistochemical analysis of paraffin-embedded Human Lung Carcinoma Tissue using S100A8+A9 ComplexMouse mAb diluted at 1:200.)
WB (Western Blot) (Western blot analysis of A) A549 Cell. B) Mouse Spleen Tissue. 3)Rat Lung Tissue Lysate using S100A8+A9 Complex Mouse mAb diluted at 1:2.000.)
IP (Immunoprecipitation) (Immunoprecipitating MYC-tag with transfected HEK293Lane 1: Mouse control IgG (1ug)instead of AAA119424 in transfected HEK293 whole cell lysate. For western blotting,a HRP-conjugated Protein G antibody was used as the secondary antibody (1/2000)Lane 2: AAA119424 (6ug)+ transfected HEK293 whole cell lysate (1mg)Lane 3: Transfected HEK293 whole cell lysate (10ug))
IF (Immunofluorescence) (Immunofluorescence staining of transfected HEK293 cells with AAA119424 at 1:100, counter-stained with DAPI. The cells were fixed in 4% formaldehyde, permeabilized using 0.2% Triton X-100 and blocked in 10% normal Goat Serum. The cells were then incubated with the antibody overnight at 4 degree C.The secondary antibody was Alexa Fluor 488-congugated AffiniPure Goat Anti-Mouse IgG (H+L).)
WB (Western Blot) (WB:Mouse anti Myc-tagged fusion protein Monoclonal antibody at 1.6ug/mlLane 1:Recombinant Myc-tagged fusion Protein at 50ngLane 2:Recombinant Myc-tagged fusion Protein at 25ngLane 3:Recombinant Myc-tagged fusion Protein at 12.5ngLane 4:Recombinant Myc-tagged fusion Protein at 6.25ngLane 5:Recombinant Myc-tagged fusion Protein at 3.125ngLane 6:Recombinant Myc-tagged fusion Protein at 1.5625ngSecondaryGoat polyclonal to Mouse IgG at 1/50000 dilutionPredicted band size: 50kdObserved band size: 50kd)
IF (Immunofluorescence) (ICC/IF analysis of PDCL3 in HeLa cells line, stained with DAPI (Blue) for nucleus staining and monoclonal anti-human PDCL3 antibody (1:100) with goat anti-mouse IgG-Alexa fluor 488 conjugate (Green). ICC/IF analysis of PDCL3 in PC3 cells line, stained with DAPI (Blue) for nucleus staining and monoclonal anti-human PDCL3 antibody (1:100) with goat anti-mouse IgG-Alexa fluor 488 conjugate (Green).)
WB (Western Blot) (Fig. 1: The extract of Jurkat (40ug), A549 (40ug) were resolved by SDS-PAGE, transferred to PVDF membrane and probed with anti-human PDCL3 antibody (1:1000). Proteins were visualized using a goat anti-mouse secondary antibody conjugated to HRP and an ECL detection system. Fig. 2: The Human Recombinant protein PDCL3 (100ng) was resolved by SDS-PAGE, transferred to PVDF membrane and probed with anti-human PDCL3 antibody (1:1000). Proteins were visualized using a goat anti-mouse secondary antibody conjugated to HRP and an ECL detection system.)
Scheme (Figure 2. A: The scheme of Anti-BCMA BiTE molecule. B: Tumor cell killing assay. NCI-H929 cells (stably transfected with luciferase), were incubated with freshly isolated human PBMC, and different concentration of BiTE antibodies constructed from rabbit Anti-Human BCMA/TNFRSF17 Clone DM4 (red line), or BB2121 originated huC11D5.3 clone (blue line) or a no BCMA binding clone as negative control (black line). After 48hrs incubation, the viable NCI-H929 tumor cells were measured by luciferase activity assay.)
Scheme (Figure 2. A: The scheme of Anti-BCMA BiTE molecule. B: Tumor cell killing assay. NCI-H929 cells (stably transfected with luciferase), were incubated with freshly isolated human PBMC, and different concentration of BiTE antibodies constructed from rabbit Anti-Human BCMA/TNFRSF17 Clone DM4 (red line), or BB2121 originated huC11D5.3 clone (blue line) or a no BCMA binding clone as negative control (black line). After 48hrs incubation, the viable NCI-H929 tumor cells were measured by luciferase activity assay.)
IHC (Immunohistochemisry) (Immunohistochemical analysis of NUCB1 protein in paraffin embedded Carcinoma of Human bladder tissue using NUCB1 antibody)
WB (Western Blot) (Western Blot analysis of HEK293T cell lysates (5 ug) transfected with either recombinant NUCB1 protein (Right) or empty vector (Left) detected with NUCB1 antibody)
FCM/FACS (Flow Cytometry) (Flow Cytometric analysis of HEK293T cells transfected with either recombinant NUCB1 protein (red) or empty vector (blue) stained using NUCB1 antibody)
IF (Immunofluorescence) (ICC/IF analysis of VIM in HeLa cells line, stained with DAPI (Blue) for nucleus staining and monoclonal anti-human VIM antibody (1:100) with goat anti-mouse IgG-Alexa fluor 488 conjugate (Green).)
WB (Western Blot) (The cell lysates (40ug) were resolved by SDS-PAGE, transferred to PVDF membrane and probed with anti-human VIM antibody (1:1000). Proteins were visualized using a goat anti-mouse secondary antibody conjugated to HRP and an ECL detection system. Lane 1 : Jurkat cell lysate Lane 2 : K562 cell lysate Lane 3 : 293T cell lysate Lane 4 : A549 cell lysate Lane 5 : SK-OV-3 cell lysate Lane 6 : HeLa cell lysate)
FCM/FACS (Flow Cytometry) (Flow cytometry analysis of KIR/CD158 in PBMC. The cell was stained at 2-5ug for 1x10^6cells (red). A Goat anti mouse IgG (Alexa fluor 488) was used as the secondary antibody. Mouse monoclonal IgG was used as the isotype control (dark gray), cells without incubation with primary and secondary antibody was used as the negative control (light gray).)
WB (Western Blot) (The cell lysates (40ug) were resolved by SDS-PAGE, transferred to PVDF membrane and probed with anti-human KIR/CD158 antibody (1:10000). Proteins were visualized using a goat anti-mouse secondary antibody conjugated to HRP and an ECL detection system.;Lane 1.: 293T cell lysate;Lane 2.: MCF7 cell lysate;Lane 3.: HepG2 cell lysate;Lane 4.: K562 cell lysate)
WB (Western Blot) (Western Blot analysis of Human cartilage lysates showing detection of SOD3 protein using Mouse Anti-SOD3 Monoclonal Antibody, Clone 4GG11G6. Primary Antibody: Mouse Anti-SOD3 Monoclonal Antibody at 1:1000. Left: Control, Middle: Young cartilage, Right: Cartilage sample with osteoarthritis-arthritis.)
ICC (Immunocytochemistry) (Immunocytochemistry/Immunofluorescence analysis using Mouse Anti-SOD3 Monoclonal Antibody, Clone 4GG11G6. Tissue: cartilage. Species: Human. Primary Antibody: Mouse Anti-SOD3 Monoclonal Antibody at 1:1000. Left: control, middle: young cartilage, right: cartilage with osteoarthritis.)
IF (Immunofluorescence) (ICC/IF analysis of NME2 in HeLa cells. The cell was stained with ATGA0475 (1:100). The secondary antibody (green) was used Alexa Fluor 488. DAPI was stained the cell nucleus (blue).)
WB (Western Blot) (The cell lysates (40ug) were resolved by SDS-PAGE, transferred to PVDF membrane and probed with anti-human NME2 antibody (1:1000). Proteins were visualized using a goat anti-mouse secondary antibody conjugated to HRP and an ECL detection system. Lane 1.: HeLa cell lysate Lane 2.: A549 cell lysate Lane 3.: MCF7 cell lysate Lane 4.: LnCap cell lysate The cell lysates (5ug) were resolved by SDS-PAGE, transferred to PVDF membrane and probed with anti-human NME2 antibody (1:1000). Proteins were visualized using a goat anti-mouse secondary antibody conjugated to HRP and an ECL detection system. Lane 1.: 293T cell lysate Lane 2.: NME2 transfected 293T cell lysate)
WB (Western Blot) (Western Blot analysis of Rat brain membrane lysate showing detection of PSD95 protein using Mouse Anti-PSD95 Monoclonal Antibody, Clone 6G6. Primary Antibody: Mouse Anti-PSD95 Monoclonal Antibody at 1:1000.)
ICC (Immunocytochemistry) (Immunocytochemistry/Immunofluorescence analysis using Mouse Anti-PSD95 Monoclonal Antibody, Clone 6G6. Tissue: dissociated hippocampal neurons. Species: Rat. Fixation: Cold 4% paraformaldehyde/0.2% glutaraldehyde in 0.1M sodium phosphate buffer. Primary Antibody: Mouse Anti-PSD95 Monoclonal Antibody at 1:1000 for 12 hours at 4 degree C. Secondary Antibody: FITC Goat Anti-Mouse IgG (green) at 1:50 for 30 minutes at RT. Magnification: 10X. Courtesy of: Mary Kennedy, Caltech.)
ICC (Immunocytochemistry) (Immunocytochemistry/Immunofluorescence analysis using Mouse Anti-PSD95 Monoclonal Antibody, Clone 6G6. Tissue: HaCaT cells. Species: Human. Fixation: Cold 100% methanol for 10 minutes at -20 degree C. Primary Antibody: Mouse Anti-PSD95 Monoclonal Antibody at 1:100 for 1 hour at RT. Secondary Antibody: FITC Goat Anti-Mouse (green) at 1:50 for 1 hour at RT. Localization: Junction staining.)
WB (Western Blot) (Western Blot analysis of Human Cervical cancer cell line (HeLa) lysate showing detection of FKBP51 protein using Mouse Anti-FKBP51 Monoclonal Antibody, Clone Hi51B. Load: 15 ug. Block: 1.5% BSA for 30 minutes at RT. Primary Antibody: Mouse Anti-FKBP51 Monoclonal Antibody at 1:1000 for 2 hours at RT. Secondary Antibody: Sheep Anti-Mouse IgG: HRP for 1 hour at RT.)
WB (Western Blot) (HepG2 cells were subjected to SDS PAGE followed by western blot with AAA102721 (CASP8 antibody) at dilution of 1:1000)
Application Data
IF (Immunofluorescence) (Immunofluorescent analysis of (-20 degree C Ethanol) fixed HeLa cells using AAA102721 (Caspase 8 Antibody) at dilution of 1:100 and Alexa Fluor 488-congugated AffiniPure Goat Anti-Mouse IgG (H+L))
IHC (Immunohistochemistry) (Immunohistochemistry of paraffin-embedded human liver cancer tissue slide using AAA102721 (Caspase 8 Antibody) at dilution of 1:200 heat mediated antigen retrieved with Tris-EDTA buffer (pH9) .)
WB (Western Blot) (Western Blot analysis of HEK293T cell lysates (5 ug) transfected with either recombinant TUBAL3 protein (Right) or empty vector (Left) detected with TUBAL3 antibody)
FCM/FACS (Flow Cytometry) (Flow Cytometric analysis of HEK293T cells transfected with either recombinant TUBAL3 protein (red) or empty vector (blue) stained using TUBAL3 antibody)
IF (Immunofluorescence) (Immunofluorescent staining of COS7 cells transiently transfected with recombinant KCTD14 protein using KCTD14 antibody)
IHC (Immunohiostchemistry) (Immunohistochemical analysis of KCTD14 protein in paraffin embedded Adenocarcinoma of Human colon tissue using KCTD14 antibody)
WB (Western Blot) (Western Blot analysis of HEK293T cell lysates (5 ug) transfected with either recombinant KCTD14 protein (Right) or empty vector (Left) detected with KCTD14 antibody)
IF (Immunofluorescence) (Immunofluorescent staining of COS7 cells transiently transfected with recombinant LOX protein using LOX antibody)
IHC (Immunohiostchemistry) (Immunohistochemical analysis of LOX protein in paraffin embedded Adenocarcinoma of Human colon tissue using LOX antibody)
WB (Western Blot) (Western Blot analysis of HEK293T cell lysates (5 ug) transfected with either recombinant LOX protein (Right) or empty vector (Left) detected with LOX antibody)
WB (Western Blot) (Western Blot analysis of HEK293T cell lysates (5 ug) transfected with either recombinant NDUFA7 protein (Right) or empty vector (Left) detected with NDUFA7 antibody)
FCM/FACS (Flow Cytometry) (Flow Cytometric analysis of HEK293T cells transfected with either recombinant NDUFA7 protein (red) or empty vector (blue) stained using NDUFA7 antibody)
FCM/FACS (Flow Cytometry) (Figure 1. ELISA plate pre-coated by 2 ug/ml (100 ul/well) Human CTLA-4 protein, mFc-His tagged protein (PME100017) can bind Rabbit anti-CTLA-4 monoclonal antibody(clone: DM50) in a linear range of 1-100 ng/ml.)
FCM/FACS (Flow Cytometry) (Figure 1. ELISA plate pre-coated by 2 ug/ml (100 ul/well) Human CTLA-4 protein, mFc-His tagged protein (PME100017) can bind Rabbit anti-CTLA-4 monoclonal antibody(clone: DM50) in a linear range of 1-100 ng/ml.)
ELISA (Figure 1. ELISA plate pre-coated by 2 ug/ml (100 ul/well) Human CTLA-4 protein, mFc-His tagged protein (PME100017) can bind Rabbit anti-CTLA-4 monoclonal antibody(clone: DM50) in a linear range of 1-100 ng/ml.)
WB (Western Blot) (Western Blot analysis of HEK293T cell lysates (5 ug) transfected with either recombinant NIF3L1 protein (Right) or empty vector (Left) detected with NIF3L1 antibody)
IHC (Immunohistochemistry) (Immunohistochemical analysis of NIF3L1 protein in paraffin embedded Adenocarcinoma of Human breast tissue using NIF3L1 antibody)
IF (Immunofluorescence) (Immunofluorescent staining of COS7 cells transiently transfected with recombinant FAM84B protein using FAM84B antibody)
WB (Western Blot) (Western Blot analysis of HEK293T cell lysates (5 ug) transfected with either recombinant FAM84B protein (Right) or empty vector (Left) detected with FAM84B antibody)
FAM84B antibody was purified by affinity chromatography.
Pricing
ICC (Immunocytochemistry) (The CCF STTG1 cell line was fixed with 5% acetic acid methanol solution for 30 minutes followed by a 5% BSA/PBS blocking. The cells were permeabilized by 0.1 % Triton x/PBS for 15 minutes and stained with Mouse Anti-Human GFAP-CY3. The slides were mounted with DAPI-Fluormount-G(R))
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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