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.
FCM/FACS (Flow Cytometry) (Flow cytometric analysis of 2% paraformaldehyde-fixed Jurkat (Human T cell leukemia cells from peripheral blood) cells labeling CD3E with M25095 at 1/200 dilution (red) compared with a mouse monoclonal IgG isotype control (black) and an unlabelled control (cells without incubation with primary antibody, blue). Goat anti-mouse IgG (FITC) at 1/300 dilution was used as the secondary antibody.)
IP (Immunoprecipitation) (CD3E was immunoprecipitated from 1mg of Jurkat cells membrane fraction, blotted with M25095 of 10 ug. Western blot was performed from the immunoprecipitate using M25095 at 1/1000 dilution. Anti-Mouse-IgG(HRP), specific to the non-reduced form of IgG, was used as secondary antibody at 1/10000 dilution. Lane 1: Jurkat cells membrane fraction. Lane2: IP product of Jurkat cells membrane fraction.Predicted band size : 23 KDaObserved band size : 23 KDaBlocking and dilution buffer and concentration:5% milk/TBST.)
IHC (Immunohiostchemistry) (Immunohistochemical analysis of ANXA10 protein in paraffin embedded Human liver tissue using ANXA10 antibody)
WB (Western Blot) (Western Blot analysis of HEK293T cell lysates (5 ug) transfected with either recombinant ANXA10 protein (Right) or empty vector (Left) detected with ANXA10 antibody)
ICC (Immunocytochemistry) (Immunostaining analysis in HeLa cells. HeLa cells were fixed with 4% paraformaldehyde and permeabilized with 0.1% Triton X-100 in PBS. The cells were immunostained with anti-BRF1 mAb. [Lot No. BRF1G2A8-2])
Quality Control #2 (Arrow indicates the region of immunized recombinant protein carrying 50-200 amino acids.)
Quality Control (Western blot analysis of immunized recombinant protein, using anti-BRF1 monoclonal antibody.)
ICC (Immunocytochemistry) (Immunostaining analysis in HeLa cells. HeLa cells were fixed with 4% paraformaldehyde and permeabilized with 0.1% Triton X-100 in PBS. The cells were immunostained with anti-TUPLE1 mAb. [Lot No.374C6a-1])
Quality Control #2 (Arrow indicates the region of immunized recombinant protein carrying 50-200 amino acids.)
Quality Control (Western blot analysis of immunized recombinant protein, using anti-TUPLE1 monoclonal antibody.)
FCM/FACS (Flow Cytometry) (Flow-cytometry using anti-human IL11RA antibody.HeLa cells were stained with an irrelevant antibody (Blue Histogram) or an anti-human IL11RA antibody monoclonal antibody (Catalog # RHG84901 ,Green Histogram) at a concentration of 5 ?ug/ml for 30 mins at RT. After washing, bound antibody was detected using a FITC conjugated goat anti-human antibody (Catalog # PHB96441) and cells analysed on a NovoCyte Flow Cytometer.)
FCM/FACS (Flow Cytometry) (Flow-cytometry using anti-human IL11RA antibody.IL11RA Transfected CHO cells were stained with an irrelevant antibody (Blue Histogram) or an anti-human IL11RA antibody monoclonal antibody (Catalog # RHG84901 ,Green Histogram) at a concentration of 5 ?ug/ml for 30 mins at RT. After washing, bound antibody was detected using a FITC conjugated goat anti-human antibody (Catalog # PHB96441) and cells analysed on a NovoCyte Flow Cytometer.)
SDS-PAGE (SDS-PAGE Analysis Purified CD86 Mouse Monoclonal Antibody (BU63) Confirmation of Integrity and Purity of Antibody.)
IF (Immunofluorescence) (mmunofluorescencestaining of PFA fixed Ramos cells using CD86 Mouse Monoclonal Antibody (BU63) followed by goat anti-mouse IgG conjugated to CF488 (green). Nuclei are stained with Reddot.)
FCM/FACS (Flow Cytometry) (Flow Cytometric Analysis of PFA fixed Ramos Cells. CD86 Mouse Monoclonal Antibody (BU63). followed byGoat anti-mouse IgG-CF488 (Blue); Isotype Control (Red).)
FCM/FACS (Flow Cytometry) (Flow Cytometric Analysis of human PBMC's Cells. usingCD86 Mouse Monoclonal Antibody (BU63); Goat anti-mouse IgG-CF488 (red); Isotype Control (green).)
IHC (Immunohistochemistry) (Formalin-fixed, paraffin-embedded human Esophageal Tumor stained with CD86 Monoclonal Antibody (BU63).)
IHC (Immunohiostchemistry) (Formalin-fixed, paraffin-embedded human Small Cell Lung Carcinoma stained with Chromogranin A Monoclonal Antibody (LK2H10))
IHC (Immunohistochemistry) (Formalin-fixed, paraffin-embedded human Adrenal Gland stained with Chromogranin A Monoclonal Antibody (LK2H10))
WB (Western Blot) (Figure 2. Western blot analysis of Tyrosine Hydroxylase using anti- Tyrosine Hydroxylase antibody (AAA44891).Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions.Lane 1: rat brain tissue lysates.After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti- Tyrosine Hydroxylase antigen affinity purified polyclonal antibody at 0.5ug/mL overnight at 4 degree C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit with Tanon 5200 system. A specific band was detected for Tyrosine Hydroxylase at approximately 59KD. The expected band size for Tyrosine Hydroxylase is at 59KD.)
IHC (Immunohistochemistry) (Figure 1. IHC analysis of Tyrosine Hydroxylase using anti- Tyrosine Hydroxylase antibody (AAA44891).Tyrosine Hydroxylase was detected in paraffin-embedded section of rat brain tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti- Tyrosine Hydroxylase Antibody (AAA44891) overnight at 4 degree C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 degree C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC) with DAB as the chromogen.)
IHC (Immunohiostchemistry) (Immunohistochemistry of 41701 in paraffin-embedded Human tonsil using 14-3-3 Rabbit mAb at dilution 1/100)
WB (Western Blot) (Western blot detection of 41701 in K562, Rat Brain,C6,3T3,Hela cell lysates using 14-3-3 Rabbit mAb(1:1000 diluted).Predicted band size:28kDa.Observed band size:28kDa.)
IHC (Immunohistochemistry) (Immunohistochemical analysis of paraffin-embedded mouse brain tissue using anti-Lysyl tRNA synthetase antibody. Counter stained with hematoxylin.)
IHC (Immunohistochemistry) (Immunohistochemical analysis of paraffin-embedded human prostate cancer tissue using anti-Lysyl tRNA synthetase antibody. Counter stained with hematoxylin.)
IHC (Immunohistochemisry) (Immunohistochemical analysis of paraffin-embedded human colon tissue using anti-Lysyl tRNA synthetase antibody. Counter stained with hematoxylin.)
IHC (Immunohiostchemistry) (Immunohistochemical analysis of paraffin-embedded rat testis tissue using anti-Lysyl tRNA synthetase antibody. Counter stained with hematoxylin.)
WB (Western Blot) (Western blot analysis of Lysyl tRNA synthetase on SiHa (1) and MCF-7 (2) cell lysate using anti-Lysyl tRNA synthetase antibody at 1/2, 000 dilution.)
ICC (Immunocytochemistry) (ICC staining Ephrin B2 in Hela 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 Ephrin B2 in 293T 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 Ephrin B2 on different tissue lysate using anti-Ephrin B2 antibody at 1/1, 000 dilution. Positive control�� Lane1: Human kidney Lane2: Mouse lung Lane3: Rat brain)
FCM/FACS (Flow Cytometry) (Flow cytometric analysis of Hela cells with PDIA6 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 PDIA6 in NIH/3T3 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 PDIA6 in HepG2 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 PDIA6 in Hela 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 PDIA6 on different lysates using anti-PDIA6 antibody at 1/1, 000 dilution. Positive control: Lane 1: HepG2 Lane 2: K562)
Application Data (Immunoperoxidase staining of formalin fixed, paraffin-embedded human placenta tissue showing cytoplasmic staining of trophoblastic cells at low (A) and high (B) magnification.)
WB (Western Blot) (Western Blot analysis of Ang-2 expression in HUV-EC-C (A) and TF-1 (B) whole cell lysates.)
IHC (Immunohiostchemistry) (Immunohistochemistry of GSK3 beta in paraffin-embedded Human Cholangiocarcinoma using GSK3 beta Rabbit mAb at dilution 1:20)
WB (Western Blot) (Western blot detection of GSK3 beta in Jurkat,C6,CHO-K1,Hela cell lysates using GSK3 beta Rabbit mAb(1:1000 diluted).Predicted band size:47kDa.Observed band size:47kDa.)
IF (Immunofluorescence) (Immunofluorescence analysis of Jurkat cells using Btk Monoclonal Antibody.)
IHC (Immunohiostchemistry) (Immunohistochemistry analysis of paraffin-embedded human lymph-node tissues (left) and human lymph follicle tissues (right). showing cytoplasmic and membrane localization with DAB staining using Btk Monoclonal Antibody.)
WB (Western Blot) (Western Blot analysis using Btk Monoclonal Antibody against K562 (1). MCF-7 (2). Jurkat (3) and HEK293 (4) cell lysate.)
WB (Western Blot) (Western Blot analysis of HEK293T cell lysates (5 ug) transfected with either recombinant PON1 protein (Right) or empty vector (Left) detected with PON1 antibody)
FCM/FACS (Flow Cytometry) (Flow Cytometric analysis of HEK293T cells transfected with either recombinant PON1 protein (red) or empty vector (blue) stained using PON1 antibody)
IHC (Immunohiostchemistry) (Immunohistochemical analysis of paraffin-embedded human lung carcinoma, using TRAF6 Antibody(AAA46897)TRAF6 was detected in paraffin-embedded tissue section. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-TRAF6 Antibody (AAA46897)overnight at 4 degree C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 degree C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC) with DAB as the chromogen.)
WB (Western Blot) (Western blot analysis of TRAF6 expression in Jurkat cell lysate (AAA46897).Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions.After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-TRAF6 monoclonal antibody overnight at 4 degree C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit with Tanon 5200 system. A specific band was detected for TRAF6)
WB (Western Blot) (Western blot analysis of NF-kB p65 expression in HeLa cell lysate (AAA46923).Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions.After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-RELA monoclonal antibody overnight at 4 degree C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit with Tanon 5200 system. A specific band was detected for RELA)
IHC (Immunohistochemistry) (Immunohistochemical analysis of paraffin-embedded human transitional cell carcinoma of bladder, using NF-kB p65 Antibody(AAA46923)RELA was detected in paraffin-embedded tissue section. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-RELA Antibody (AAA46923)overnight at 4 degree C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 degree C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC) with DAB as the chromogen.)
WB (Western Blot) (Western blot analysis of Topoisomerase II alpha expression in (1) HeLa cell lysate; (2) Jurkat cell lysate (AAA47007).Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions.After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-TOP2A monoclonal antibody overnight at 4 degree C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit with Tanon 5200 system. A specific band was detected for TOP2A)
IHC (Immunohistochemistry) (Immunohistochemical analysis of paraffin-embedded human colon cancer, using Topoisomerase II alpha Antibody(AAA47007)TOP2A was detected in paraffin-embedded tissue section. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-TOP2A Antibody (AAA47007)overnight at 4 degree C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 degree C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC) with DAB as the chromogen.)
IHC (Immunohistochemistry) (Formaldehyde-fixed paraffin-embedded (FFPE) Tissue Slides. Human heart ventricle following immunostaining with cMHC 3-48 and irrelevant Neuro monoClonal antibody at low microscopical magnification. A: cMHC 3-48-labeled cardiomyocytes. FFPE section of human heart ventricle was submitted to HIAR condition with citrate B buffer prior to immunostaining. Immunostaining was revealed following incubation with biotinylated goat anti-mouse IgG, 20 minutes at 20C and horse radish peroxidase-diaminobemzidine enzymatic reaction causing brown precipitate to appear atthe sites of primary antibody binding. B: Control immunostaining performed following HIAR condition on the same microscopical slide with Neuro monoclonal antibody showing no immunostaining but presence of light background, emphasizing specificity of immunostaining in (A). Magnification x30 C: Fragment of the same slide as in (A) with heart ventricle cardiomyocytes immunostained (brown). Magnification x580)
Cardiac Myosin Heavy Chain Mouse Monoclonal (3-48_G5C7)
Gene Names
MYH7; CMH1; MPD1; SPMD; SPMM; CMD1S; MYHCB
Reactivity
Human, Rat, Mouse Predicted: Canine, Bovine and Rabbit
Applications
Immunohistochemistry, Immunofluorescence, Western Blot
Pricing
Application Data (Sandwich ELISA: In combination with anti-human IL-17A clone 4C1 coated ELISA plate, the anti-human IL-17A antibody clone 3H11, when conjugated with Biotin, can be used for quantitative measurement of human IL-17A in sandwich ELISA. The dynamic range of the standard curve is 1000pg/ml to 15.6pg/ml.)
FCM/FACS (Flow Cytometry) (Flow Cytometry / FACS analysis: Detection of ATPase Na+/K+ alpha 1 in fixed Hela cells)
Application Data (Image: Immunocytochemistry: Detection of ATPA1 (Green) in HepG2 cells using ATPase Na+/K+ alpha 1. Nuclei (Blue) were counterstained using Hoechst 33258.)
WB (Western Blot) (Western Blotting: Detection of ATPase Na+/K+ alpha 1 in in porcine proximal tubule protein)
FCM/FACS (Flow Cytometry) (Flow cytometry analysis of PPARGC1A in HeLa cells. The cell was stained with AAA48935 at 2-5ug for 1x106cells (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).)
IF (Immunofluorescence) (ICC/IF analysis of PPARGC1A in HeLa cells. The cell was stained with AAA48935 (1:100). The secondary antibody (green) was used Alexa Fluor 488. DAPI was stained the cell nucleus (blue).)
WB (Western Blot) (The cell and tissue lysates (40ug) were resolved by SDS-PAGE, transferred to PVDF membrane and probed with anti-human PPARGC1A 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 lysateLane 2.: MCF7 cell lysateLane 3.: HepG2 cell lysateLane 4.: 293T cell lysateLane 5.: Mouse brain tissue lysate)
ELISA (Figure 2 ELISA Validation of HIV-1 p24 Antibody with HIV-1 p24 Protein Coating Antigen: HIV-1 p24 recombinant protein, 1ug/mL, incubated at 4 degree C overnight. Detection Antibodies: HIV-1 p24 antibody, PM-6329, dilution: 0.3-1000 ng/mL, incubated at RT for 1 hr. Secondary Antibodies: Goat anti-mouse HRP at 1:5,000, incubated at RT for 1 hr.)
WB (Western Blot) (Figure 1 Western Blot Validation with HIV-1 p24 Protein Loading: 30 ng HIV-1 p24 recombinant protein. Antibodies: HIV-1 p24, PM-6329, 0.5ug/mL, 1h incubation at RT in 5% NFDM/TBST. Secondary: Goat anti-mouse IgG HRP conjugate at 1:5,000 dilution.)
FCM/FACS (Flow Cytometry) (Flow Cytometric analysis using CCR7 antibodyStaining of C57BL/6 splenocytes with CD4 antibody (FITC) and 0.5 ug of Rat IgG2a kappa Isotype Control (biotin) (left) or 0.5 ug of CD197 antibody (biotin) (right) followed by Streptavidin (PE). Staining with CD197 antibody was carried out at 37deg C for 0.5 hours and Fc receptor binding was blocked by staining cells with CD16/CD32 antibody. Cells in the lymphocyte gate were used for analysis.)
FCM/FACS (Flow Cytometry) (Flow Cytometric analysis using CCR7 antibodyStaining of C57BL/6 splenocytes with CD4 antibody (FITC) and 0.5 ug of Rat IgG2a kappa Isotype Control (biotin) (left) or 0.5 ug of CD197 antibody (biotin) (right) followed by Streptavidin (PE). Staining with CD197 antibody was carried out at 37deg C for 0.5 hours and Fc receptor binding was blocked by staining cells with CD16/CD32 antibody. Cells in the lymphocyte gate were used for analysis.)
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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