At AAA Biotech, we provide a broad range of purified polyclonal antibodies (pAbs) that are able to all be browsed online through our website. Due to their high specificity and strong binding affinity, these antibodies are ideal for wide swathes of research and experimental applications.
Our polyclonal antibodies can easily support your work, whether you use them for Western Blotting, Immunocytochemistry (with or without Immunofluorescence used in conjunction), Immunohistochemistry, Immunoprecipitation, and ELISA tests. We highly encourage you to browse our range of pAbs and choose the one that best suits your experimental model.
IF (Immunofluorescence) (Immunofluorescence analysis of HeLa cells using SMO Polyclonal Antibody (AAA10769) at dilution of 1:100 (40x lens). Blue: DAPI for nuclear staining.)
IF (Immunofluorescence) (Immunofluorescence analysis of C6 cells using SMO Polyclonal Antibody (AAA10769) at dilution of 1:100 (40x lens). Blue: DAPI for nuclear staining.)
IHC (Immunohistochemistry) (Immunohistochemistry of paraffin-embedded rat brain using SMO antibody (40x lens).)
WB (Western Blot) (Western blot analysis of extracts of Mouse brain, using SMO antibody (AAA10769) at 1:500 dilution.Secondary antibody: HRP Goat Anti-Rabbit IgG (H+L) at 1:10000 dilution.Lysates/proteins: 25ug per lane.Blocking buffer: 3% nonfat dry milk in TBST. Detection: ECL Basic Kit. Exposure time: 180s)
WB (Western Blot) (Western blot analysis of extracts of various cell lines, using SMO antibody (AAA10769) at 1:500 dilution.Secondary antibody: HRP Goat Anti-Rabbit IgG (H+L) at 1:10000 dilution.Lysates/proteins: 25ug per lane.Blocking buffer: 3% nonfat dry milk in TBST. Detection: ECL Enhanced Kit. Exposure time: 120s)
WB (Western Blot) (Western blot analysis of extracts of various cell lines, using SMO antibody at 1:1000 dilution.Secondary antibody: HRP Goat Anti-Rabbit IgG (H+L) at 1:10000 dilution.Lysates/proteins: 25ug per lane.Blocking buffer: 3% nonfat dry milk in TBST.Detection: ECL Enhanced Kit.Exposure time: 30s)
IF (Immunofluorescence) (AAA31072 staining HeLa by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100, then blocked in 10% serum for 45 minutes at 25 degree C. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37 degree C. An Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibody.)
IF (Immunofluorescence) (AAA31072 staining COS7 cells by ICC/IF. Cells were fixed with PFA and permeabilized in 0.1% saponin prior to blocking in 10% serum for 45 minutes at 37 degree C. The primary antibody was diluted 1/400 and incubated with the sample for 1 hour at 37 degree C. A Alexa Fluor 594 conjugated goat polyclonal to rabbit IgG (H+L), diluted 1/600 was used as secondary antibody.)
IHC (Immunohistochemistry) (AAA31072 at 1/100 staining Mouse liver tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22 degree C. An HRP conjugated goat anti-rabbit antibody was used as the secondary.)
WB (Western Blot) (Western blot analysis of Phospho-LKB1 (Ser428) Antibody expression in PMA treated Hela cells lysates.The lane on the right is treated with the antigen-specific peptide.)
WB (Western Blot) (Western blot analysis of LKB1 phosphorylation expression in PMA treated HeLa whole cell lysates, The lane on the left is treated with the antigen-specific peptide.)
IF (Immunofluorescence) (Immunofluorescence analysis of U-251MG cells using VHL Polyclonal Antibody (AAA10644) at dilution of 1:100 (40x lens). Blue: DAPI for nuclear staining.)
IHC (Immunohistochemistry) (Immunohistochemistry analysis of paraffin-embedded human kidney using VHL Rabbit pAb at dilution of 1:100 (40x lens).Perform high pressure antigen retrieval with 10 mM citrate buffer pH 6.0 before commencing with IHC staining protocol.)
WB (Western Blot) (Western blot analysis of extracts of various cell lines, using VHL antibody (AAA10644) at 1:1000 dilution.Secondary antibody: HRP Goat Anti-Rabbit IgG (H+L) at 1:10000 dilution.Lysates/proteins: 25ug per lane.Blocking buffer: 3% nonfat dry milk in TBST.Detection: ECL Basic Kit.Exposure time: 30s.)
IHC (Immunohistochemistry) (Immunohistochemistry of paraffin-embedded human rectal cancer using MMP25 antibody at dilution of 1:200 (40x lens).)
IHC (Immunohistochemistry) (Immunohistochemistry of paraffin-embedded human lung cancer using MMP25 antibody at dilution of 1:200 (40x lens).)
WB (Western Blot) (Western blot analysis of extracts of various cell lines, using MMP25 antibody (AAA10688) at 1:400 dilution. Secondary antibody: HRP Goat Anti- Rabbit IgG (H+L) at 1:10000 dilution. Lysates/proteins: 25ug per lane.Blocking buffer: 3% nonfat dry milk in TBST)
IHC (Immunohistochemistry) (Immunohistochemistry of SMURF2 in human uterus tissue with SMURF2 antibody at 2 ug/ml)
IF (Immunofluorescence) (Immunofluorescence of SMURF2 in mouse liver tissue with SMURF2 antibody at 20 ug/ml. Green: SMURF2 Antibody (AAA10972) Blue: DAPI staining.)
IHC (Immunohistochemistry) (Immunohistochemistry of SMURF2 in mouse liver tissue with SMURF2 antibody at 2 μg/ml.)
IF (Immunofluorescence) (Immunofluorescence of SMURF2 in human uterus tissue with SMURF2 antibody at 20 μg/ml.Green: SMURF2 Antibody (AAA10972)Blue: DAPI staining)
IF (Immunofluorescence) (Immunofluorescence of SMURF2 in mouse liver tissue with SMURF2 antibody at 20 μg/mL.)
IHC (Immunohistochemistry) (Immunohistochemistry of SMURF2 in mouse liver tissue with SMURF2 antibody at 5 μg/mL.)
IF (Immunofluorescence) (Immunofluorescence of SHANK3 in human brain tissue with SHANK3 antibody at 20 μg/mL.)
IHC (Immunohistochemistry) (Immunohistochemistry of SHANK3 in human brain tissue with SHANK3 antibody at 2.5 μg/mL.)
WB (Western Blot) (Western blot analysis of SHANK3 in 3T3 cell lysate with SHANK3 antibody at 1 μg/ml in (A) the absence and (B) the presence of blocking peptide.)
IHC (Immunohistochemistry) (Figure 8 Immunohistochemistry Validation of ATF6 in Rat Brain Tissue Immunohistochemical analysis of paraffin-embedded Rat brain tissue using anti-ATF6 antibody (AAA10937) at 5 ug/ml. Tissue was fixed with formaldehyde and blocked with 10% serum for 1 h at RT; antigen retrieval was by heat mediation with a citrate buffer (pH6). Samples were incubated with primary antibody overnight at 4°C. A goat anti-rabbit IgG H&L (HRP) at 1/250 was used as secondary. Counter stained with Hematoxylin.)
IHC (Immunohistochemistry) (Figure 7 Immunohistochemistry Validation of ATF6 in Mouse Brain Tissue Immunohistochemical analysis of paraffin-embedded mouse brain tissue using anti-ATF6 antibody (AAA10937) at 5 ug/ml. Tissue was fixed with formaldehyde and blocked with 10% serum for 1 h at RT; antigen retrieval was by heat mediation with a citrate buffer (pH6). Samples were incubated with primary antibody overnight at 4°C. A goat anti-rabbit IgG H&L (HRP) at 1/250 was used as secondary. Counter stained with Hematoxylin.)
IF (Immunofluorescence) (Figure 6 Immunofluorescence Validation of ATF6 in Human Testis Cells Immunofluorescent analysis of 4% paraformaldehydefixed human testis labeling ATF6 with AAA10937 at 20 ug/mL, followed by goat anti-rabbit IgG secondary antibody at 1/500 dilution (green) and DAPI staining (blue).)
IF (Immunofluorescence) (Figure 5 Immunofluorescence Validation of ATF6 In A549 Cells Immunofluorescent analysis of 4% paraformaldehydefixed A549 cells labeling ATF6 with AAA10937 at 20 ug/mL, followed by goat anti-rabbit IgG secondary antibody at 1/500 dilution (green) and DAPI staining (blue).)
WB (Western Blot) (Loading: 15 ug of rat kidney lysate Antibodies: ATF6 (AAA10937), 1 ug/mL , 1 h incubation at RT in 5% NFDM/TBST. Secondary: Goat Anti-Rabbit IgG HRP conjugate at 1:10000 dilution.)
WB (Western Blot) (Figure 3 WB Validation in Mouse Tissue Loading: 15 ug of mouse tissue lysate Antibodies: ATF6 (AAA10937), 1 ug/mL , 1 h incubation at RT in 5% NFDM/TBST. Secondary: Goat Anti-Rabbit IgG HRP conjugate at 1:10000 dilution.)
WB (Western Blot) (Figure 2 WB Validation in Human Cell Lines Loading: 15 ug of human cell lysate Antibodies ATF6 (AAA10937), 1 ug/mL , 1 h incubation at RT in 5% NFDM/TBST. Secondary: Goat Anti-Rabbit IgG HRP conjugate at 1:10000 dilution. Secondary: Goat Anti-Rabbit IgG HRP conjugate at 1:10000 dilution. conjugate at 1:10000 dilution.Secondary: Goat Anti-Rabbit IgG HRP conjugate at 1:10000 dilution. conjugate at 1:10000 dilution.)
WB (Western Blot) (Loading: 15 ug of human HeLa cell lysate Antibodies ATF6 (150934), 0.5 ug/mL , 1 h incubation at RT in 5% NFDM/TBST. Secondary: Goat Anti-Rabbit IgG HRP conjugate at 1:10000 dilution.)
Western Blot, Immunohistochemistry, Immunofluorescence
Purity
IL-9 Antibody is affinity chromatography purified via peptide column.
Pricing
WB (Western Blot) (Western blot analysis of extracts of various cell lines, using BMPR1A antibody (AAA10766) at 1:1000 dilution.Secondary antibody: HRP Goat Anti-Rabbit IgG (H+L) at 1:10000 dilution.Lysates/proteins: 25ug per lane.Blocking buffer: 3% nonfat dry milk in TBST.Detection: ECL Enhanced KitExposure Time: 90s)
IHC (Immunohistchemistry) (Immunohistochemistry of paraffin-embedded human trachea using ATPIF1 antibody at dilution of 1:100 (40x lens).)
IHC (Immunohistochemistry) (Immunohistochemistry of paraffin-embedded human liver cancer using ATPIF1 antibody at dilution of 1:100 (40x lens).)
IHC (Immunohistochemistry) (Immunohistochemistry of paraffin-embedded human stomach using ATPIF1 antibody at dilution of 1:100 (40x lens).)
IP (Immunoprecipitation) (Immunoprecipitation analysis of 300 ug extracts of K-562 cells using 3ug [KO Validated] ATPIF1 Rabbit pAb (AAA10772). Western blot was performed from theimmunoprecipitate using [KO Validated] ATPIF1 Rabbit pAb (AAA10772) at a dilution of 1:3000)
IF (Immunofluorescence) (Immunofluorescence analysis of U2OS cells using [KO Validated] ATPIF1 Rabbit pAb (AAA10772) at dilution of 1:100. Secondary antibody: Cy3 Goat Anti-Rabbit IgG (H+L) at 1:500 dilution. Blue: DAPI for nuclear staining)
WB (Western Blot) (Western blot analysis of lysates from wild type(WT) and ATPIF1 knockout (KO) 293T(KO)cells, using [KO Validated] ATPIF1 Rabbit pAb (AAA10772) at 1:1000 dilution.Secondary antibody: HRP Goat Anti-Rabbit IgG (H+L) (at 1:10000 dilution. Lysates/proteins: 25?g per lane. Blocking buffer: 3% nonfat dry milk in TBST. Detection: ECL Basic Kit Exposure time: 1s.)
IHC (Immunohistchemistry) (Immunohistochemistry of paraffin-embedded human brain using Myelin Basic Protein Rabbit pAb (AAA10723) at dilution of 1:100 (40x lens).)
IHC (Immunohistochemistry) (Immunohistochemistry of paraffin-embedded rat brain using Myelin Basic Protein Rabbit pAb (AAA10723) at dilution of 1:100 (40x lens))
IHC (Immunohistochemistry) (Immunohistochemistry of paraffin-embedded mouse brain using Myelin Basic Protein Rabbit pAb (AAA10723) at dilution of 1:100 (40x lens))
IHC (Immunohistochemistry) (Immunohistochemistry of paraffin-embedded mouse kidney using MBP antibody at dilution of 1:200 (40x lens).)
IHC (Immunohistochemistry) (Immunohistochemistry of paraffin-embedded rat kidney using MBP antibody at dilution of 1:200 (40x lens).)
WB (Western Blot) (Western blot analysis of extracts of various cell lines, using MBP antibody at 1:1000 dilution.Secondary antibody: HRP Goat Anti-Rabbit IgG (H+L) at 1:10000 dilution.Lysates/proteins: 25ug per lane.Blocking buffer: 3% nonfat dry milk in TBST.)
IF (Immunofluorescence) (Immunofluorescence analysis of MCF-7 cells using MID1 antibody (AAA28180). Blue: DAPI for nuclear staining.)
WB (Western Blot) (Western blot analysis of extracts of HeLa cells, using MID1 Rabbit pAb (AAA28180) at 1:1000 dilution.Secondary antibody: HRP Goat Anti-Rabbit IgG (H+L) at 1:10000 dilution.Lysates/proteins: 25ug per lane. Blocking buffer: 3% nonfat dry milk in TBST.Detection: ECL Basic Kit (RM00020).Exposure time: 60s.)
WB (Western Blot) (Western blot analysis of extracts of various cell lines, using MID1 antibody (AAA28180) at 1:1000 dilution.Secondary antibody: HRP Goat Anti-Rabbit IgG (H+L) at 1:10000 dilution.Lysates/proteins: 25ug per lane.Blocking buffer: 3% nonfat dry milk in TBST.Detection: ECL Enhanced Kit.Exposure time: 90s.)
IHC (Immunohistochemistry) (Immunohistochemistry of paraffin-embedded human liver cancer using CYP24A1 antibody at dilution of 1:200 (40x lens).)
IHC (Immunohistochemistry) (Immunohistochemistry of paraffin-embedded human liver cancer using CYP24A1 antibody at dilution of 1:200 (40x lens).)
IHC (Immunohistchemistry) (Immunohistochemistry of paraffin-embedded mouse kidney using CYP24A1 antibody at dilution of 1:200 (40x lens).)
IHC (Immunohistochemistry) (Immunohistochemistry of paraffin-embedded rat pancreas using CYP24A1 antibody at dilution of 1:200 (40x lens).)
IHC (Immunohistochemistry) (Immunohistochemistry of paraffin-embedded rat kidney using CYP24A1 antibody at dilution of 1:200 (40x lens).)
IHC (Immunohistochemistry) (Immunohistochemistry of paraffin-embedded rat lung using CYP24A1 antibody at dilution of 1:200 (40x lens).)
WB (Western Blot) (Western blot analysis of extracts of Mouse kidney, using CYP24A1 antibody (AAA10721) at 1:1000 dilution.Secondary antibody: HRP Goat Anti-Rabbit IgG (H+L) at 1:10000 dilution.Lysates/proteins: 25ug per lane. Blocking buffer: 3% nonfat dry milk in TBST. Detection: ECL Enhanced Kit. Exposure time: 180s.)
WB (Western Blot) (Western blot analysis of extracts of various cell lines, using CYP24A1 antibody at 1:1000 dilution.Secondary antibody: HRP Goat Anti-Rabbit IgG (H+L) at 1:10000 dilution.Lysates/proteins: 25ug per lane.Blocking buffer: 3% nonfat dry milk in TBST.)
IHC (Immunohistochemistry) (EIF2S1 Antibody (N-term) (Cat. #AAA28744)immunohistochemistry analysis in formalin fixed and paraffin embedded human stomach tissue followed by peroxidase conjugation of the secondary antibody and DAB staining.This data demonstrates the use of EIF2S1 Antibody (N-term) for immunohistochemistry. Clinical relevance has not been evaluated.)
IF (Immunofluorescence) (Confocal immunofluorescent analysis of EIF2S1 Antibody (N-term) (Cat#AAA28744) with Hela cell followed by Alexa Fluor 488-conjugated goat anti-rabbit lgG (green). DAPI was used to stain the cell nuclear (blue).)
WB (Western Blot) (EIF2S1 Antibody (N-term) (Cat. #AAA28744) western blot analysis in mouse bladder tissue lysates (35ug/lane).This demonstrates the EIF2S1 antibody detected the EIF2S1 protein (arrow).)
IF (Immunofluorescence) (Figure 12 Immunohistochemistry Validation of PD-L1in Human Tumors (Gadiot et al., 2011)Immunohistochemical analysis of patient tumors labeling PD-L1 with anti-PD-L1 antibodies (AAA10941). Several anti-PD-L1 antibodies were tested for staining, “Only 1 antibody gave no background staining and was competitively blocked by the addition of PD-L1Fc protein (AAA10941)”.)
IF (Immunofluorescence) (Figure 11 Immunofluorescence Validation of PD-L1 intumors in Human Cells (Dhar et al., 2018)(A) Several antibody brands were first tested with RBCs,WBCs, and HeLa cells. (AAA10941) was chosen as it provided the highest staining intensity. (B, C) Using the optimal conditions of anti-PDL1 at a concentration of 50ug/mL, following by goat anti-rabbit Alexa Fluor 647, PDL-1 staining was tested on several lung cancer cell lines: (adenocarcinoma), adenocarcinoma), (squamous) and WBCs asa control. (D) Once validated, patient samples were stained for PD-L1, CK, CD45, DAPI.)
IF (Immunofluorescence) (Figure 10 Immunofluorescence Validation of PD-L1 in Rat HeartImmunofluorescence analysis of 4% paraformaldehyde-fixed rat heart tissue labeling PD-L1 with AAA10941 at 20 ug/ml,followed by goat anti-rabbit IgG secondary antibody at 1/250 dilution (red).)
IHC (Immunohistchemistry) (Figure 9 Immunohistochemistry Validation of PD-L1 in Human HeartImmunohistochemical analysis of paraffin-embedded human heart tissue using anti-PD-L1 antibody (AAA10941) at 2.5 °g/ml. Tissue was fixed with formalde hyde and blocked with 10% serum for 1 h at RT; antigen retrieval was by heat mediation with a citrate buffer (pH6). Samples were incubated with primary antibody overnight at 4°C. A goat anti-rabbit IgG H&L (HRP) at 1/250 was used assecondary. Counter stained with Hematoxylin.)
IHC (Immunohistochemistry) (Figure 8 Immunohistochemistry Validation of PD-L1 in Rat HeartImmunohistochemical analysis of paraffin-embedded rat heart tissue using anti-PD-L1 antibody (AAA10941) at 5 ug/ml.Tissue was fixed with formaldehyde and blocked with 10% serum for 1 h at RT; antigen retrieval was by heat mediation with a citrate buffer (pH6). Samples were incubated with primary antibody overnight at 4°C. A goatanti-rabbit IgG H&L (HRP) at 1/250 was used as secondary.Counter stained with Hematoxylin)
FCM (Flow Cytometry) (Figure 7 Flow Cytometry Validation of PD-L1Overlay histogram showing A-20 cells stained with AAA10941 (red line, 1ug/1x106 cells). 1 h incubation at 4°C in 2% FBS/PBS. Followed by secondary antibody 488 goat anti-rabbit IgG (H+L) at 1/500 dilution for 1 h 4°C. Isotype control antibody (Green line) was mouse IgG1 (1ug/1x106 cells) used under the same conditions. Acquisition of >10,000 events was performed.)
IF (Immunofluorescence) (Figure 6 Immunofluorescence Validation of PD-L1 in Human HeartImmunofluorescent analysis of 4% paraformaldehyde-fixed human heart tissue labeling PD-L1 with AAA10941 at 20μg/mL, followed by goat anti-rabbit IgG secondaryantibody at 1/500 dilution (red). Image showing both membrane and cytoplasmic staining on human heart tissue.)
IHC (Immunohistochemistry) (Figure 5 Immunohistochemistry Validation of PD-L1 in Human Tonsil CellsImmunohistochemical analysis of paraffin-embedded human tonsil tissue using anti-PD-L1 antibody (AAA10941) at 5ug/ml. Tissue was fixed with formalde hyde and blocked with 10% serum for 1 h at RT; antigen retrieval was by heat mediation with a citrate buffer (pH6). Samples were incubated with primary antibody overnight at 4°C. A goat anti-rabbit IgG H&L (HRP) at 1/250 was used as secondary. Counter stained with Hematoxylin.)
WB (Western Blot) (Figure 4 Validation with PD-L1 over expression in 293 cellsLoading: Lysates/proteins at 15 μg per lane. Lane 1: non-transfected 293 cells Lane 2: PD-L1 overexpressed 293 cells Antibodies: AAA10941 (1 μg/mL). 1 h incubation at RT in 5% NFDM/TBST. Secondary: Goat anti-rabbit IgGHRP conjugate at 1:10000 dilution.)
WB (Western Blot) (Figure 3 Validation with PD-L1 siRNA Knockdown in HeLa CellsHeLa cells were transfected with control siRNAs (lane 1) orPD-L1 siRNAs (lane 2) Loading: 10 ug of HeLa whole cell lysates per lane. Antibodies: (2 ug/mL) and GAPDH (, 0.02 ug/mL), 1 h incubation at RT in 5% NFDM/TBST. Secondary: Goat anti-mouse IgG HRP conjugate at 1:5000 dilution.)
WB (Western Blot) (Figure 2 Independent Antibody Validation (IAV) via Protein Expression Profile in Human and Mouse cell linesLoading: 15 ug of lysates per lane. Antibodies: AAA10941 (2ug/mL), (2 ug/mL), and beta-actin (1 ug/mL), 1 h incubation at RT in 5% NFDM/TBST. Secondary: Goat anti-rabbit and or anti-mouse IgG HRP conjugate at 1:10000 and 1:5000 dilution, respectively.)
WB (Western Blot) (Figure 1 Western Blot Validation of PD-L1 in HeLa CellsLoading: 15ug of lysates per lane. Antibodies: AAA10941 (1 ug/mL), 1 h incubation at RT in 5% NFDM/TBST. Secondary: Goat anti-rabbit IgG HRP conjugate at 1:10000 dilution.)
IF (Immunofluorescence) (Confocal immunofluorescence analysis of U2OS cells using TOMM40 Polyclonal Antibody at dilution of 1:200. Blue: DAPI for nuclear staining.)
WB (Western Blot) (Western blot analysis of extracts of various cell lines, using TOMM40 antibody at 1:1000 dilution.Secondary antibody: HRP Goat Anti-Rabbit IgG (H+L) at 1:10000 dilution.Lysates/proteins: 25ug per lane.Blocking buffer: 3% nonfat dry milk in TBST.Detection: ECL Basic Kit.Exposure time: 60s.)
Western Blot, Immunohistochemistry, Immunofluorescence, Immunocytochemistry
Purity
Affinity Purification
Pricing
What are Polyclonal Antibodies?
Polyclonal antibodies are antibodies that come from multiple B cell clones of a host animal. The typical hosts used for the majority of polyclonal antibody production are rabbits, goats, sheep, and donkeys. These polyclonal antibodies, once having identified their target, will bind to different epitopes located at different regions or sequences on the same protein/antigen. As a result, they are ideal at locating and binding to the target, even if the target is in very low concentrations (due to many different antibodies being able to bind to the same target molecule, which allows for significant amplification of a downstream signal).
Polyclonal antibodies are typically produced by injecting an antigen into a host animal, which causes the animal’s immune system to attack the foreign antigen by mass generating antibodies against it. After a period of time, serum is collected from the animal and purified using physicochemical fractionation, class-specific affinity purification, and/or antigen-affinity purification.
Key Uses of Polyclonal Antibodies
Western Blotting: This method is used to find specific proteins in biological samples after separating them by size.
Immunohistochemistry: IHC helps visualize the location of proteins in tissue sections using various staining techniques.
ELISA: (Enzyme-Linked Immunosorbent Assay) is typically used to identify specific protein quantities in a sample. ELISAs can be either “Quantitative” or “Qualitative”.
Flow Cytometry: technique that identifies and measures the specific protein on the surface or inside the cells in a fluid suspension.
Immunoprecipitation: IP isolates and studies a specific protein from a complex mixture using antibodies.
Why Buy Polyclonal Antibodies from AAA Biotech?
1. Ideal for Various Applications
Our antibodies are generally going to be validated for use in multiple types of assays, including ELISA, Western Blotting, Immunohistochemistry, Immunoprecipitation, amongst others. They are ideal for a wide range of research applications.
2. Rigorous Quality Control
All of the antibodies in our catalog undergo strict quality testing to ensure specificity, sensitivity, and consistent performance. We are confident in the ability of our antibodies to provide you with accurate results.
3. Wide Assortment of Antibodies
Antibodies in are catalog can be found for both common and exotic species, and these antibodies are also available in both conjugated and recombinant forms to suit many diverse experimental needs.
4. Highly Purified
Our antibodies are available in purified forms with over 85% purity, as confirmed by SDS-PAGE. They are also available with tags such as His, Flag, GST, or MBP. We cater to customers worldwide.
FAQ
1. How are polyclonal antibodies produced?
Traditionally, polyclonal antibodies are produced by injecting an antigen into a host animal (such as a rabbit or goat), which then triggers an immune response from the host animal. The animal’s B cells produce antibodies that will recognize different parts of the injected antigen. These antibodies are then collected from the animal’s blood and purified for use.
2. How do polyclonal antibodies differ from monoclonal antibodies?
Polyclonal antibodies are a mix of antibodies that bind to different locations (epitopes) of the same antigen, while monoclonal antibodies are identical and bind to just one specific epitope. This makes polyclonal antibodies more versatile and better at detecting proteins that may be present in low quantities or in altered/modified forms.
3. How should I store polyclonal antibodies?
Polyclonal antibodies should be stored at 4°C for short-term use (up to a few weeks) and at -20°C or -80°C for long-term storage. Avoid repeated freeze-thaw cycles by dividing them into small aliquots. Always check the datasheet for specific storage instructions.
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