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) (Immunocytochemistry staining of HeLa cells fixed with 4% Paraformaldehyde and using TBLR1 mouse mAb (dilution 1:200).)
IHC (Immunohistochemistry) (IHC of paraffin-embedded huma breast cancer using anti-TBLR1 mouse mAb diluted 1/500-1/1000)
WB (Western Blot) (Western blot detection of TBLR1 in Mouse brain.Mouse heart and K562 cell lysates using TBLR1 mouse mAb (1:1000 diluted).Predicted band size: 60KDa.Observed band size: 60Kda.)
WB (Western Blot) (Western blot detection of TBLR1 in Hela and K562 cell lysates using TBLR1 mouse mAb (1:1000 diluted).Predicted band size: 60KDa.Observed band size: 60Kda.)
IF (Immunofluorescence) (Immunofluorescence analysis of Mouse-liver tissue. 1.CD21 Monoclonal Antibody(2C5)(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 (Immunohistochemistry) (Immunohistochemical analysis of paraffin-embedded Rat-kidney tissue. 1.CD21 Monoclonal Antibody(2C5) 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 (Immunohistochemisry) (Immunohistochemical analysis of paraffin-embedded Mouse-kidney tissue. 1.CD21 Monoclonal Antibody(2C5) 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 (Immunohiostchemistry) (Immunohistochemical analysis of paraffin-embedded Human-stomach tissue. 1.CD21 Monoclonal Antibody(2C5) 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) (IHC staining of human tonsil tissue. diluted at 1:200.)
IHC (Immunohistochemistry) (Immunohistochemical analysis of paraffin-embedded Rat-heart tissue. 1.CD1 Monoclonal Antibody(9H6) 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 (Immunohistochemisry) (Immunohistochemical analysis of paraffin-embedded Mouse-heart tissue. 1.CD1 Monoclonal Antibody(9H6) 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 (Immunohiostchemistry) (Immunohistochemical analysis of paraffin-embedded human-tonsils using antibody diluted at 1:50.)
IHC (Immunohistochemistry) (Immunohistochemical analysis of paraffin-embedded Human-Tonsil tissue. 1.CD1 Monoclonal Antibody(9H6) 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 (Immunohiostchemistry) (Immunohistochemical analysis of paraffin-embedded Human-liver tissue. 1.CD16 Monoclonal Antibody(Q32) 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) Jurkat. 2) K562. diluted at 1:2000.)
IHC (Immunohistochemistry) (Immunohistochemical analysis of paraffin-embedded Human-lung-cancer tissue. 1.CD15 Monoclonal Antibody(Q89) 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 (Immunohistochemisry) (Immunohistochemical analysis of paraffin-embedded Human stomach. 1. Antibody was diluted at 1:200(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 stomach. 1. Antibody was diluted at 1:200(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 (Immunohistochemistry) (Immunohistochemical analysis of paraffin-embedded Human stomach. 1. Antibody was diluted at 1:200(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).)
IF (Immunofluorescence) (Immunofluorescence analysis of Rat-heart tissue. 1.Histone H2B Monoclonal Antibody(Mix)(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)
IF (Immunofluorescence) (Immunofluorescence analysis of Mouse-kidney tissue. 1.Histone H2B Monoclonal Antibody(Mix)(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)
IF (Immunofluorescence) (Immunofluorescence analysis of Human-liver-cancer tissue. 1.Histone H2B Monoclonal Antibody(Mix)(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)
IF (Immunofluorescence) (Immunofluorescence analysis of Hela cell. 1.Brp44L Polyclonal Antibody(green) was diluted at 1:200(4 degree overnight). (red) was diluted at 1:200(4 degree overnight). 2. Goat Anti Rabbit Alexa Fluor 488 was diluted at 1:1000(room temperature. 50min). Goat Anti Mouse Alexa Fluor 594 was diluted at 1:1000(room temperature. 50min).)
WB (Western Blot) (Western blot analysis of 1) Hela. 2) 3T3. 3) Raw264.7. 4) Rat Brain. 5) Rat Kidney. diluted at 1:2000. cells nucleus extracted by Minute TM Cytoplasmic and Nuclear Fractionation kit (SC-003.Inventbiotech.MN.USA).)
WB (Western Blot) (Western blot analysis of lysates from 1) Rat Heart Tissue. 2) huvec.3) Jurkat cells. (Green) primary antibody was diluted at 1:1000. 4 degree over night. secondary antibodywas diluted at 1:10000. 37 degree 1hour. (Red) Actin ? Polyclonal Antibody antibody was diluted at 1:5000 as loading control. 4 degree over night.secondary antibodywas diluted at 1:10000. 37 degree 1hour.)
Application Data (The picture was kindly provided by our customer)
IHC (Immunohiostchemistry) (Immunohistochemical analysis of paraffin-embedded Human Breast Carcinoma Tissue using NFAT5 Mouse Monoclonal antibody diluted at 1:500.)
WB (Western Blot) (Western blot analysis of 1)Hela Cell. 2) Mouse Brain. 3) Rat Brain Tissue Lysate using NFAT5Mouse Monoclonal mAb diluted at 1:2.000.)
WB (Western Blot) (Western blot analysis of 1)PC12 Cell. 2) Mouse Brain Tissue Lysate using Tyrosine HydrolaseMouse Monoclonal mAb diluted at 1:2.000.)
WB (Western Blot) (Western blot analysis of 1)HepG2 Cell. 2) HepG2 Treated with CoCl2 cell Lysate using HIF-1?Mouse Monoclonal mAb diluted at 1:2.000.)
IHC (Immunohistochemistry) (Immunohistochemical analysis of paraffin-embedded Mouse Brain Tissue using STAT3Mouse mAb diluted at 1:200.)
IHC (Immunohistochemisry) (Immunohistochemical analysis of paraffin-embedded Human Colon Carcinoma using STAT3Mouse mAb diluted at 1:200.)
WB (Western Blot) (Western blot detection of STAT3 in human breast cancer cell line MCF-7(A). T47D(B). MDA-MB-231(C) and Cal51 (D) using STAT3 mouse mAb (AAA320494. 1:2000 diluted).Predicted band size: 86kDa.Observed band size:86kDa. Picture was kindly provided by our customer from Tianjin Medical University Cancer Institute and Hospital)
WB (Western Blot) (Western blot analysis of 1) Rat Heart Tissue. 2)Mouse Heart Tissue. 3) Hela with STAT3 Mouse mAb diluted at 1:2.000.)
IHC (Immunohistochemisry) (Immunohistochemical analysis of paraffin-embedded Human Pancreatic Carcinoma using Cyclophilin BMouse mAb diluted at 1:200.)
IHC (Immunohiostchemistry) (Immunohistochemical analysis of paraffin-embedded Human Heptacarcinoma using Cyclophilin BMouse mAb diluted at 1:200.)
WB (Western Blot) (Western blot analysis of 1) Hela. 2)Jurkat. 3)293T. 4)Rat Liver Tissue. 5) 3T3. 6) HepG2 with Cyclophilin B Mouse mAb diluted at 1:2.000.)
IF (Immunofluorescence) (Immunofluorescence analysis of mouse-spleen tissue. 1.PPAR Delta Mouse Monoclonal Antibody(2F9)(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 (Immunohistochemisry) (Immunohistochemical analysis of paraffin-embedded Mouse Brain Tissue using PPAR Delta Mouse mAb diluted at 1:200.)
IHC (Immunohiostchemistry) (Immunohistochemical analysis of paraffin-embedded Human-uterus tissue. 1.PPAR Delta Mouse Monoclonal Antibody(2F9) 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 Brain Tissue using PPAR Delta Mouse mAb diluted at 1:200.)
IF (Immunofluorescence) (Immunofluorescence analysis of rat-spleen tissue. 1.NBR1 Mouse Monoclonal Antibody(7C3)(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 (Immunohistochemisry) (Immunohistochemical analysis of paraffin-embedded Rat-lung tissue. 1.NBR1 Mouse Monoclonal Antibody(7C3) 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 (Immunohiostchemistry) (Immunohistochemical analysis of paraffin-embedded Human-liver tissue. 1.NBR1 Mouse Monoclonal Antibody(7C3) 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 Skeletal Muscle Tissue using NBR1 Mouse mAb diluted at 1:200.)
Application Data (Ma, Zhan, Shuping Lou, and Zheng Jiang. "PHLDA2 regulates EMT and autophagy in colorectal cancer via the PI3K/AKT signaling pathway." Aging (Albany NY) 12.9 (2020): 7985.)
IHC (Immunohistochemistry) (Immunohistochemical analysis of paraffin-embedded human tonsil. 1, Tris-EDTA,pH9.0 was used for antigen retrieval. 2 Antibody was diluted at 1:200(4 degree overnight.3,Secondary antibody was diluted at 1:200(room temperature, 45min).)
WB (Western Blot) (Western blot analysis of 1 293T cell, 2 293T Transfected ACE2 CellLysate using ACE2 Mouse Monoclonla Antibody diluted at 1:50,000.)
IHC (Immunohiostchemistry) (Immunohistochemical analysis of paraffin-embedded Human Kidney Tissue using ACE2 Mouse monoclonal antibody diluted at 1:200.)
IF (Immunofluorescence) (IF analysis of 293T Transfected ACE2 CellLysate using ACE2 Mouse Monoclonla Antibody diluted at 1:500.)
WB (Western Blot) (Western blot analysis of 1) Jurkat, 2) 293T, 3) Rat Brain Tissue, 4) Mouse Brain Tissue with Phosphotyrosine Mouse mAb diluted at 1:2,000)
IHC (Immunohistochemistry) (Immunohistochemical analysis of paraffin-embedded Human Breast Caricnoma using PhosphotyrosineMouse mAb diluted at 1:200.)
SDS-PAGE (Various whole cell lysates were separated by 10% SDS-PAGE, and the membrane was blotted with anti-IL-1?(PTR2541) antibody. The HRP-conjugated Goat anti-M)
SDS-PAGE (Whole cell lysates of A549 were separated by 10% SDS-PAGE, and the membrane was blotted with anti-Integrin ?3(PTR2555) antibody. The HRP-conjugated Goat anti-M)
SDS-PAGE (Whole cell lysates were separated by 10% SDS-PAGE, and the membrane was blotted with anti-GSK3?/?(PTR2350) antibody. The HRP-conjugated Goat anti-M)
SDS-PAGE (Whole cell lysates were separated by 10% SDS-PAGE, and the membrane was blotted with anti-CD19 (PTR2046) antibody. The HRP-conjugated Goat anti-M)
ICC (Immunocytochemistry) (Immunocytochemistry of HeLa cells using anti-CDC2/CDK1 mouse mAb diluted 1:50.)
WB (Western Blot) (Western blot detection of CDC2/CDK1 in K562.A549.Jurkat and Hela cell lysates using CDC2/CDK1 mouse mAb (1:100 diluted).Predicted band size: 34KDa.Observed band size: 34KDa.)
ICC (Immunocytochemistry) (Immunocytochemistry staining of HeLa cells fixed with 4% Paraformaldehyde and using SAFB1 mouse mAb (dilution 1:200).)
WB (Western Blot) (Western blot detection of SAFB1 in HelaNE.A431.MDA-MB-468.Breast cancer.ZR75-1 and MCF7 cell lysates using SAFB1 mouse mAb (1:4000 diluted).Predicted band size: 130kDa.Observed band size: 130kDa.)
ICC (Immunocytochemistry) (Immunocytochemistry staining of HeLa cells fixed with -20? Methanol and using Fyn mouse mAb (dilution 1:50).)
WB (Western Blot) (Western blot detection of Fyn in Hela.3T3.C6.COS7.CEM.Ramos and Jurkat cell lysates using Fyn mouse mAb (1:500 diluted).Predicted band size:59KDa.Observed band size:59KDa.)
ICC (Immunocytochemistry) (Immunocytochemistry staining of HeLa cells fixed with 4% Paraformaldehyde and using TORC1 mouse mAb (dilution 1:200).)
WB (Western Blot) (Western blot detection of TORC1 in Hela.mouse brain.SW480.COS7.C6 and 3T3 cell lysates using TORC1 mouse mAb (1:2000 diluted).Predicted band size:78KDa.Observed band size:78KDa.)
IP (Immunoprecipitation) (Immunoprecipitation analysis of Hela cell lysate using SWAP70 mouse mAb.)
WB (Western Blot) (Western blot detection of SWAP70 in COS7.293T.C6.3T3 and Hela cell lysates and using SWAP70 mouse mAb (1:1000 diluted).Predicted band size: 70KDa.Observed band size: 70KDa.)
IP (Immunoprecipitation) (Immunoprecipitation analysis of Hela and 3T3 cell lysates using RAD9A mouse mAb.)
WB (Western Blot) (Western blot detection of RAD9A in Hela.MCF7.3T3.COS7 and Rat testis cell lysates using RAD9A mouse mAb (1:500 diluted).Predicted band size:43KDa.Observed band size:55KDa.)
IP (Immunoprecipitation) (Immunoprecipitation analysis of Hela cell lysates using PEG10 mouse mAb.)
WB (Western Blot) (Western blot detection of PEG10 in Hela cell lysates using PEG10 mouse mAb (1:1000 diluted).Predicted band size:55KDa.Observed band size:55KDa.95KDa.)
IF (Immunofluorescence) (Immunofluorescent analysis of A549 cells fixed with 4% Paraformaldehyde and using anti-Lamin A/C mouse mAb (dilution 1:200).)
WB (Western Blot) (Western blot detection of Lamin A/C in MCF7.A549 and Hela cell lysates using Lamin A/C mouse mAb (1:1000 diluted).Predicted band size:74.63KDa.Observed band size:74.63KDa.)
IF (Immunofluorescence) (Immunofluorescent analysis of Phosphorylation of H2A.X at Serine 139 in A549(upper.untreated or Hydroxyurea-treated) and Hela(lower.untreated or Hydroxyurea-treated) using Phospho-Histone H2A.X (Ser139) mouse mAb (1:400).)
IF (Immunofluorescence) (Immunofluorescent analysis of Phosphorylation of H2A.X at Serine 139 in 3T3 or Hydroxyurea-treated 3T3 cells using Phospho-Histone H2A.X)
WB (Western Blot) (Western blot detection of Phosphorylation of H2A.X at Serine 139 in 3T3 or Hydroxyurea-treated 3T3 cell lysates using Phospho-Histone H2A.X (Ser139) mouse mAb (1:2000 diluted).Predicted band size:15KDa.Observed band size:15KDa.)
WB (Western Blot) (Western blot analysis of extracts from untreated or Hydroxyurea-treated Hela and A549 cells. using Histone H2A.X(Phospho-Ser139) mouse mAb (1:1000 diluted)(upper) or ?-Actin Mouse mAb (200068-8F10)(lower).Predicted band size:15KDa.Observed band size:15KDa.)
ICC (Immunocytochemistry) (Immunocytochemistry staining of Hela cells fixed with 4% Paraformaldehyde and using anti-MAP2(N-term) mouse mAb (dilution 1:100).)
IP (Immunoprecipitation) (Immunoprecipitation analysis of Hela cell lysates using MAP2 (N-terminus) mouse mAb.)
WB (Western Blot) (Western blot detection of MAP2(N-terminus) in Mouse Brain tissue and Hela cell lysates using MAP2(N-terminus) mouse mAb (1:1000 diluted).Predicted band size: 202KDa.Observed band size: 300KDa.)
IHC (Immunohiostchemistry) (Immunohistochemistry analysis of paraffin-embedded ovarian cancer (left) and kidney cancer (right) with DAB staining using MEK-6 Monoclonal Antibody.)
WB (Western Blot) (Western Blot analysis using MEK-6 Monoclonal Antibody against HepG2 (1). MCF-7 (2) and NIH/3T3 (3) cell lysate.)
IHC (Immunohiostchemistry) (Immunohistochemistry analysis of paraffin-embedded ovarian cancer (left) and lung cancer (right) with DAB staining using p63 Monoclonal Antibody.)
WB (Western Blot) (Western Blot analysis using p63 Monoclonal Antibody against A431 (1). HeLa (2). Jurkat (3). THP-1 (4). NIH/3T3 (5). Cos7 (6) and PC-12 (7) cell lysate.)
FCM/FACS (Flow Cytometry) (Flow cytometric analysis of Jurkat cells using PARP-1 Monoclonal Antibody (green) and negative control (purple).)
WB (Western Blot) (Western Blot analysis using PARP-1 Monoclonal Antibody against Jurkat (1). K562 (2). HeLa (3). Raji (4).THP-1 (5) and SW620 (6) cell lysate.)
IF (Immunofluorescence) (Confocal immunofluorescence analysis of methanol-fixed HepG2 cells using PEG10 Monoclonal Antibody (green). showing cytoplasmic localization. Blue: DRAQ5 fluorescent DNA dye.)
IHC (Immunohiostchemistry) (Immunohistochemistry analysis of paraffin-embedded human Placenta tissues with AEC staining using PEG10 Monoclonal Antibody.)
WB (Western Blot) (Western Blot analysis using PEG10 Monoclonal Antibody against truncated Trx-PEG10 recombinant protein (1).truncated GST-PEG10 (aa1-120) recombinant protein (2) and full-length PEG10 (aa1-325)-hIgGFc transfected CHO-K1 cell lysate (3).)
IHC (Immunohiostchemistry) (Immunohistochemistry analysis of paraffin-embedded ovarian cancer (A). stomach cancer (B) with DAB staining using PLAP Monoclonal Antibody.)
WB (Western Blot) (Western Blot analysis using PLAP Monoclonal Antibody against HepG2 (1). A431 (2) and MCF-7 (3) cell lysate.)
Immunofluorescence, Immunohistochemistry, Western Blot
Purity
Affinity purification
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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