Many protein analysis techniques utilize antibodies to detect analytes in complex biological samples. The antibodies used in these immunoassays, such as immunocytochemistry (ICC), immunohistochemistry (IHC), flow cytometry, Western blot, and ELISA, are typically conjugated to enzymatic or fluorescent labels that produce signals to visualize analyte detection. Both primary and secondary antibodies can be conjugated. The decision to use a conjugated primary antibody versus a conjugated secondary antibody is dependent upon whether the protein is being detected by direct or indirect methods.
- Direct detection is a one-step labeling procedure. It uses a primary conjugated antibody to identify the target analyte.
- Indirect detection is a two-step labeling procedure. It utilizes an unconjugated primary antibody to bind to the target protein. A secondary antibody is then used to detect the bound primary antibody and produce the signal.
Bio-Techne offers an extensive collection of primary conjugated antibodies for your research needs.
Benefits of Using a Primary Conjugated Antibody
Less Background Staining
Using a conjugated primary antibody for direct detection of analytes eliminates any non-specific binding that may occur with secondary antibodies, thereby reducing background signals.
Species Cross-Reactivity Minimized
Using a primary conjugated antibody for direct detection of analytes minimizes species cross-reactivity that may occur with secondary antibodies.
Procedures Simplified
Using a conjugated primary antibody for direct detection of analytes shortens protocols as only one labeling step is required.
Fluorescent Conjugates Available from Bio-Techne
Fluorescent conjugates use fluorochromes to produce a fluorescent signal. They become excited by absorbing a specific wavelength of light. The excited fluorescent dye will then emit light at a longer wavelength. Fluorescent-conjugated primary antibodies can be used for multiplex techniques including immunofluorescence, flow cytometry, and FACS. Additionally, fluorescently labeled primary antibodies are ideal tools for multiplexing. The key is to choose fluorophores that have distinct absorption and emission spectra so that there is no cross-channel fluorescence. Bio-Techne offers a wide variety of fluorescent-labeled primary antibodies. Explore our antibodies by type of fluorescent conjugate.
Bio-Techne offers a wide variety of fluorescent-labeled primary antibodies. Explore our antibodies by type of fluorescent conjugate.
Commonly Used Fluorescent Conjugates for Primary Antibodies
Fluorescent Conjugate | Excitation Wavelength (nm) | Emission Wavelength (nm) | Emission Color |
---|---|---|---|
DyLight 405 | 400 | 420 | Blue |
Alexa Fluor® 405 | 401 | 421 | Blue |
DyLight 350 | 353 | 432 | Blue |
Alexa Fluor 350 | 346 | 442 | Blue |
mFluor™ Violet 450 | 406 | 445 | Blue |
mFluor Violet 500 | 410 | 501 | Green |
NorthernLights™ 493 | 493 | 514 | Green |
DyLight 488 | 493 | 518 | Green |
Fluorescein (FITC) | 498 | 519 | Green |
Alexa Fluor 488 | 490 | 525 | Green |
Alexa Fluor 532 | 532 | 554 | Yellow |
Janelia Fluor® 549 | 549 | 571 | Yellow |
Phycoerythrin (PE) | 498, 565 | 573 | Yellow |
NorthernLights 557 | 557 | 574 | Yellow |
DyLight 550 | 562 | 576 | Yellow |
mFluor Violet 610 | 421 | 613 | Orange |
Alexa Fluor 594 | 590 | 617 | Orange |
DyLight 594 | 593 | 618 | Orange |
PE/Atto594 | 498,566 | 632 | Red |
NorthernLights 637 | 637 | 658 | Red |
Allophycocyanin (APC) | 650 | 660 | Red |
Janelia Fluor 646 | 646 | 664 | Red |
Alexa Fluor 647 | 653 | 669 | Red |
DyLight 650 | 652 | 672 | Red |
PerCP | 488 | 675 | Red |
PE/Cy5.5 | 498, 566 | 700 | Red |
DyLight 680 | 692 | 712 | Near Infrared |
Alexa Fluor 700 | 696 | 720 | Near Infrared |
Alexa Fluor 750 | 749 | 775 | Near Infrared |
PE/Cy7 | 489, 566 | 782 | Near infrared |
APC/Cy7 | 652 | 790 | Near infrared |
Enzyme Conjugates Available from Bio-Techne
In addition to fluorescent conjugates, antibodies can also be conjugated to enzymes such as horseradish peroxidase (HRP) and alkaline phosphatase (AP). These enzymes catalyze chromogenic substrates to produce an insoluble, colored precipitate at the site of the antibody-antigen complex. Though the range of colored signals is not as extensive as that with fluorescent conjugates, chromogenic detection of analytes offers several advantages over fluorescence including being amenable to light microscopy and producing a longer lasting signal. Chromogenic detection is ideal for IHC, Western blot, and ELISA.
View Our HRP-Conjugated Primary Antibodies
View Our AP-Conjugated Primary Antibodies
Products for Signal Amplification
Biotin-Conjugated Antibodies
Biotin-Conjugated Antibodies
If the expression of the target analyte is low, Biotin-conjugated antibodies can be used, in conjunction with a labeled-Streptavidin molecule, to amplify the detection signal.
Streptavidin Conjugates
Streptavidin Conjugates
Chromogenic- or fluorescent-conjugated Streptavidin is used with Biotin-conjugated antibodies to detect low expressed analytes. A single Streptavidin molecule can bind up to four Biotins, thus amplifying the detection signal.
VisUCyte™ HRP Polymer
VisUCyte™ HRP Polymer
The VisUCyte HRP Polymer from R&D Systems, a Bio-Techne brand, is a Biotin-free detection reagent for IHC. It overcomes the problems related to the Avidin-Biotin detection chemistry, thus producing cleaner IHC results.
Additional Antibody Products
Antibody Labeling Kits
Antibody Labeling Kits
The Lightning-Link™ Antibody Labeling Kits from Novus allows you to label primary antibodies in less than 30 seconds hands-on time. Over 40 fluorescent, enzymatic, and biotin labels are available.
Isotype Control Antibodies
Isotype Control Antibodies
We offer isotype control antibodies for negative controls. Our selection includes unconjugated- and conjugated- antibodies for many species and antibody isoforms.
Flow Cytometry Workflow Solutions
Flow Cytometry Workflow Solutions
We offer a range of products for the entire flow cytometry workflow. Explore our portfolio of flow-validated antibodies and multicolor flow cytometry kits.
Additional Antibody Resources
Immunohistochemistry (IHC) Handbook
Immunohistochemistry (IHC) Handbook
Download Bio-Techne’s IHC Handbook to get information on techniques, protocols, and troubleshooting methods to help with your IHC experiment.
Flow Cytometry Handbook
Flow Cytometry Handbook
Download Bio-Techne’s Flow Cytometry Handbook to get detailed protocols and troubleshooting information for flow cytometry experiments.
Western Blot Handbook
Western Blot Handbook
Request this Western Blot Handbook from Novus to learn more about techniques, protocols, and troubleshooting tips for Western blot.
FAQs
Labeling chemistries often exploit primary amine groups to covalently attach labels to antibody molecules. The N-terminus of polypeptide chains and the side chain of lysine amino acid residues contain primary amines. It is possible to link labels to antibodies by using chemical groups that react with amines. The four main chemical approaches for antibody labeling are summarized below:
- NHS Esters: In the case of fluorescent dyes, it is typical to purchase an activated form of the dye with an inbuilt NHS ester (also called a ‘succinimidyl ester’). Linking the activated dye to an antibody by chemical conjugation occurs under physiological or alkaline conditions to generate stable amide bonds. Excess reactive dye is removed by one of several possible methods, often column chromatography before the labeled antibody is used in an immunoassay.
Find out more about reactivity of fluorescent dyes.
- Heterobifunctional Reagents: If the label is a protein molecule (e.g. HRP, alkaline phosphatase, or phycoerythrin), then the antibody labeling procedure is complicated by the fact that both the antibody and label contain multiple amine groups. To restrict conjugation to the antibody, lysine residues on the antibody are modified to create a new reactive group (X), while lysine residues on the label are modified to create another reactive group (Y). A ‘heterobifunctional reagent’ is used to introduce the Y groups, which subsequently react with X groups when the antibody and label are mixed, thus creating heterodimeric conjugates. There are many variations on this theme.
- Carbodiimides: Carbodiimides are commonly used to conjugate antibodies to carboxylated particles (e.g. latex particles, magnetic beads) and to other carboxylated surfaces, such as microwell plates or chip surfaces. Carbodiimides are rarely used to attach dyes or protein labels to antibodies, although they are important in the production of NHS-activated dyes (see above).These reagents are used to create covalent links between amine- and carboxyl-containing molecules. Carbodiimides activate carboxyl groups, and the activated intermediate is then attacked by an amine (e.g. provided by a lysine residue on an antibody).
- Sodium Periodate: Although this chemical is not compatible with the majority of labels, it is applicable to HRP, the most popular diagnostic enzyme. Periodate activates carbohydrate chains on the HRP molecule to create aldehyde groups, which are capable of reacting with lysine residues on antibody molecules. Since HRP itself has very few lysine residues, it is relatively easy to create antibody-HRP conjugates without significant HRP polymerization.
Why DyLight®?
DyLight® Fluorescent Dyes are a family of high-intensity, photostable fluorescent tags for labeling antibodies and other molecular probes, which may be used for flow cytometry, ELISA, fluorescence microscopy, and other array platforms. DyLight® dyes have absorption maxima ranging from 350nm-800nm, covering the entire visible light spectrum as well as several key near-IR and IR wavelengths. DyLight® dyes are trusted and relied on by researchers around the globe.
DyLight® Antibody Labeling Kits
Lightning-Link® Rapid DyLight® Antibody Labeling Kits combine the quick labeling efficiency of Lightning-Link® antibody labeling technology with the trust and stability of the DyLight® dye brand. Label your antibody or protein directly with a Lightning-Link® Rapid DyLight® Antibody Labeling Kit - 10 different DyLight® dyes are available.
A tandem dye, also called a FRET pair or FRET dye, is a pair of covalently linked fluorescent molecules, comprising a donor and an acceptor molecule. The donor molecule emits energy that is absorbed by the acceptor molecule through a phenomenon known as Förster- or fluorescence-resonance energy transfer (FRET). FRET is a technique widely used in biology, to study for example protein-protein interactions, membrane fluidity and receptor-ligand binding.
To learn more about tandem dyes read our Tandem Dye Conjugated Antibodies FAQs.