HRP conjugation / labeling in < 4 hrs with 30 secs hands-on time using HRP Conjugation Kit ab102890. 100% antibody recovery.
Rapid, reproducible HRP antibody conjugation kit (also compatible with other proteins and peptides):
Fast, easy protocol - add modifier to antibody and incubate for 3 hrs, then add quencher for 30 mins
HRP labeled antibody is ready for use in applications like WB, ELISA, and IHC, with no need for further purification
Compatible with most standard antibody formulations
Scalable; use the same conjugation method from 10µg-100mg of antibody
Use Lightning-Link® conjugation with over 45 labels, including Alexa Fluor®, DyLight®, tandem dyes, enzymes, oligonucleotides, and gold nanoparticles
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Publications
- Frontiers in immunology 14:13076932023Novel S2 subunit-specific antibody with broad neutralizing activity against SARS-CoV-2 variants of concern.Applications:Unspecified applicationReactive species:Unspecified reactive speciesChang-Kyu Heo,Won-Hee Lim,Jihyun Yang,Sumin Son,Sang Jick Kim,Doo-Jin Kim,Haryoung Poo,Eun-Wie ChoPubMed 38143750
- Microorganisms 11:2023Humoral Immune Responses in Patients with Severe COVID-19: A Comparative Pilot Study between Individuals Infected by SARS-CoV-2 during the Wild-Type and the Delta Periods.Applications:Unspecified applicationReactive species:Unspecified reactive speciesMaria Sukhova,Maria Byazrova,Artem Mikhailov,Gaukhar Yusubalieva,Irina Maslova,Tatyana Belovezhets,Nikolay Chikaev,Ivan Vorobiev,Vladimir Baklaushev,Alexander FilatovPubMed 37764191
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HRP conjugation / labeling in < 4 hrs with 30 secs hands-on time using HRP Conjugation Kit ab102890. 100% antibody recovery.
Rapid, reproducible HRP antibody conjugation kit (also compatible with other proteins and peptides):
Fast, easy protocol - add modifier to antibody and incubate for 3 hrs, then add quencher for 30 mins
HRP labeled antibody is ready for use in applications like WB, ELISA, and IHC, with no need for further purification
Compatible with most standard antibody formulations
Scalable; use the same conjugation method from 10µg-100mg of antibody
Use Lightning-Link® conjugation with over 45 labels, including Alexa Fluor®, DyLight®, tandem dyes, enzymes, oligonucleotides, and gold nanoparticles
Storage
- Shipped at conditions
Ambient - Cannot Ship with Ice
- Appropriate short-term storage conditions
-20°C
- Appropriate long-term storage conditions
-20°C
- Storage information
-20°C
Notes
HRP Conjugation Kit / HRP Labeling Kit ab102890 uses a simple and quick process for HRP labeling / conjugation of antibodies. It can also be used to conjugate other proteins or peptides. Learn about our . To conjugate an antibody to HRP using this kit: - add modifier to antibody and incubate for 3 hrs - add quencher and incubate for 30 mins The HRP conjugated antibody can be used immediately in WB, ELISA, IHC etc. No further purification is required and 100% of the antibody is recovered for use. Learn about buffer compatibility below; for incompatible buffers and low antibody concentrations, use our rapid . Use the to learn more about the technology, or about conjugating other proteins and peptides to HRP. Custom size conjugation kits up to 100 mg are available on demand. Please contact us to discuss your requirements.
This product is manufactured by Expedeon, an Abcam company, and was previously called Lightning-Link® HRP Labeling Kit. 701-0004 is the same as the 5 mg size. 701-0003 is the same as the 5 x 1 mg size. 701-0000 is the same as the 3 x 100 ug size. 701-0030 is the same as the 3 x 10 ug size. 701-0010 is the same as the 100 μg size. 701-0002 is the same as the 1 mg size.
Amount and volume of antibody for conjugation to HRP
| Kit size | Recommended amount of antibody1 | Maximum amount of antibody | Maximum antibody volume2 |
| 3 x 10 μg | 3 x 10 μg | 3 x 40 μg | 3 x 10 μL |
| 100 μg | 1 x 100 μg | 1 x 400 μg | 1 x 100 μL |
| 3 x 100 μg | 3 x 100 μg | 3 x 400 μg | 3 x 100 μL |
| 1 mg | 1 x 1 mg | 1 x 4 mg | 1 x 1 mL |
| 5 x 1 mg | 5 x 1 mg | 5 x 4 mg | 5 x 1 mL |
| 5 mg | 1 x 5 mg | 1 x 20 mg | 1 x 5 mL |
1 Recommended amount of antibody will give an HRP:antibody molar ratio of 4:1. Antibodies often also perform well at the maximum amount of antibody which is 1:1 molar ratio.
2 Ideal antibody concentration is 1mg/ml. 0.5 - 1 mg/ml can be used if the maximum antibody volume is not exceeded. Antibodies > 4 mg/ml or < 0.5 mg/ml should be diluted /concentrated.
Buffer Requirements for Conjugation
Buffer should be pH 6.5-8.5.
Buffer constituent compatibility
If a concentration is shown, then the constituent should be no more than the concentration shown. If several constituents are close to the limit of acceptable concentration, then this can inhibit conjugation.
| Compatible buffer constituents | ||
| 50mM / 0.6% Tris1 | 0.1% BSA | 50% glycerol |
| 0.1% sodium azide2 | PBS | Potassium phosphate |
| Sodium chloride | HEPES | Sucrose |
| Sodium citrate | EDTA | Trehalose |
1 Tris buffered saline is almost always ≤ 50 mM / 0.6%
2 Sodium azide irreversibly inhibits HRP; antibodies with azide should be purified before using the HRP conjugation kit.
| Incompatible buffer constituents | ||
| Thiomerosal | Proclin | Glycine |
| Arginine | Glutathione | DTT |
If a constituent of the buffer containing your antibody or protein is not listed above, please contact us.
Only purified antibodies are suitable for use, ie. where other proteins, peptides, or amino acids are not present: antibodies in ascites fluid, serum or hybridoma culture media are incompatible.
Storing and handling conjugation kits
Lyophilized Lightning-Link® components are hygroscopic.
Kits are intentionally shipped at ambient temperature with silica gel to avoid exposure to moisture. Upon receipt, store the kit frozen and protect from moisture. Before opening the outer container, allow the lyophilized components to reach room temperature to minimize condensation.
Product promise
We are dedicated to supporting your work with high quality reagents and we are here for you every step of the way should you need us.
In the unlikely event of one of our products not working as expected, you are covered by our product promise.
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9 product images
Image from Parkash, Om, et al., Diagnostics (Basel), 11(1):33; doi: 10.3390/diagnostics11010033. Reproduced under the Creative Commons license https://creativecommons.org/licenses/by/4.0/Conjugation - HRP Conjugation Kit - Lightning-Link® (ab102890)
Parkash, Om, et al used HRP Conjugation Kit - Lightning-Link® (ab102890) as part of the development and evaluation of a biosensor based on screen-printed carbon electrodes (SPCEs) for the detection of dengue-specific immunoglobulin M (IgM) antibodies. They used the kit to conjugate HRP to anti-dengue antibody for use in conjugation.
(A) Schematic diagram of the screen printed carbon electrode (SCPE)-based dengue IgM biosensor. The biosensor was constructed by sequentially adding optimised concentration of anti-human IgM capture antibody, blocking agent, human IgM antibody or serum sample, dengue antigen and detection antibody, with washing steps in between. Electrochemical signal was generated following addition of TMB substrate. (B) Comparison of various immobilisation techniques for the goat anti-human IgM capture antibody. NC: negative control consisting of a dengue IgM negative serum sample; PC: dengue IgM positive serum sample. (C) Field Emission Scanning Electron Microscopy (FESEM) surface images of (left panel) a bare carbon electrode and (right panel) a carbon electrode modified with an anti-human IgM antibody using the streptavidin/biotin immobilisation system. Both capture and detection antibodies were labeled using Lightning-Link® conjugation kits (Biotinylation Kit / Biotin Conjugation Kit (Fast, Type B) - Lightning-Link® ab201796 and ab102890).
Image from Rackus et al., Lab Chip., 17(13):2272-2280; doi: 10.1039/c7lc00440k.Reproduced under the Creative Commons license https://creativecommons.org/licenses/by/3.0/Conjugation - HRP Conjugation Kit - Lightning-Link® (ab102890)
Rackus, Darius G., et al used HRP Conjugation Kit - Lightning-Link® (ab102890) as part of examining digital microfluidics for detection a malaria biomarker. They used the kit to conjugate HRP to anti-Plasmodium falciparum LDH antibody for use in pre-concentration by liquid intake by paper (P-CLIP).
DMF immunoassay for PfLDH. Comparison of mean signals obtained by traditional DMF-ELISA (black) and P-CLIP modified DMF-ELISA (grey) for concentrations below the limit of detection (7 ng mL-1) and limit of quantitation (70 ng mL-1) of the traditional DMF-ELISA. Error bars ± 1 std. dev. (n = 3).
Image from Lemaire, Katleen, et al., PloS one, 6(4): e18517; doi: 10.1371/journal.pone.0018517. Reproduced under the Creative Commons license https://creativecommons.org/licenses/by/4.0/Western blot - HRP Conjugation Kit - Lightning-Link® (ab102890)
Lemaire, Katleen, et al used HRP Conjugation Kit - Lightning-Link® (ab102890) as part of examining protein interactions. They used the kit to conjugate HRP to anti-BIP and anti-UFBP1 antibodies for use in detection by western blot after immunoprecipitation.
Co-immunoprecipitation with BiP, UFL1 and UFM1 specific antibodies. BiP and UFBP1 antibodies were conjugated to HRP using ab102890 for detection after immunoprecipitation.
Image from Cervin, Jakob, et al., PLoS pathogens?14.2 (2018): e1006862. Reproduced under the Creative Commons license https://creativecommons.org/licenses/by/4.0/ELISA - HRP Conjugation Kit - Lightning-Link® (ab102890)
ELISA - HRP Conjugation Kit Lightning-Link.
Cervin, Jakob, et al used HRP Conjugation Kit - Lightning-Link® (ab102890) as part of examining binding of Cholera Toxin subunit B (CTB) to blood group antigen LewisX (LeX). They used the kit to conjugate HRP to CTB and G33D (mutated version of CTB) for use in ELISA.
ELISA with titrated amounts human serum albumin-linked oligosaccharides (HSA-OS), immobilized to wells and detected with (B) CTB-HRP and (C) G33D-HRP. Graph shows absorbance values from three independent experiments.
Image from Gram M et al.,PLoS One, 10(9):e0138111. Fig 1.; doi: 10.1371/journal.pone.0138111. Reproduced under the Creative Commons license https://creativecommons.org/licenses/by/4.0/Conjugation - HRP Conjugation Kit - Lightning-Link® (ab102890)
HRP Conjugation Kit - Lightning-Link® labeling monoclonal and polyclonal rabbit IgG for ELISA.
Gram M et al. used ab102890 to assess levels of cell free fetal haemoglobin (HbF) and haptoglobin (Hp) by ELISA.
Samples were from normal pregnancies (Control) and women diagnosed with PE. The cell-free HbF plasma concentration of each patient sample (Control and PE) was plotted against the Hp plasma concentration.
Image from Rasmussen DG et al., PLoS One, 12(1):e0170023. Fig 2.; doi: 10.1371/journal.pone.0170023. Reproduced under the Creative Commons license https://creativecommons.org/licenses/by/4.0/Conjugation - HRP Conjugation Kit - Lightning-Link® (ab102890)
HRP Conjugation Kit - Lightning-Link® labeling C3C antibody for competitive ELISA.
Rasmussen DG et al. used ab102890 to determine levels of C3C by competitive ELISA.
(A) Standard curve and inhibition of the competitive ELISA signal using healthy human serum, (B) human heparin plasma and (C) human EDTA plasma. The native material was run from undiluted and up to 8-fold diluted as indicated. (D) Neo-epitope specificity of the C3C ELISA was shown by comparing reactivity towards an elongated peptide, i.e. a peptide with an additional amino acid at the N-terminal generated by cleavage, a non-sense peptide, i.e. a peptide with a different sequence, and the standard peptide. The standard peptide (i.e. standard curve), elongated peptide, and non-sense peptide were diluted 2-fold from 100 ng/mL. The data is presented as percent (%) of background absorbance, which is the absorbance with only assay buffer present, as a function of peptide concentration.
Image from Laura RP et al., PloS One, 11(2):e0149391. Fig 2.; doi: 10.1371/journal.pone.0149391. Reproduced under the Creative Commons license https://creativecommons.org/licenses/by/4.0/Conjugation - HRP Conjugation Kit - Lightning-Link® (ab102890)
HRP Conjugation Kit - Lightning-Link® labeling polyclonal goat and Mab-16E3 anti-MPO antibodies for ELISA.
Laura RP et al. used ab102890 to determine concentrations of MPO by ELISA.
The relative amounts of secreted versus cellular myeloperoxidase (MPO) were calculated for each cell line.
Image from Kristensen JH et al., BMC Pulm Med., 15:53. Fig 3.; doi: 10.1186/s12890-015-0048-5. Reproduced under the Creative Commons license https://creativecommons.org/licenses/by/4.0/Conjugation - HRP Conjugation Kit - Lightning-Link® (ab102890)
HRP Conjugation Kit - Lightning-Link® labeling monoclonal EL-NE antibody for competitive ELISA.
Kristensen JH et al. used ab102890 for the quantification of neutrophil elastase (NE)-degraded elastin (EL).
EL-NE fragment levels in serum from patients with IPF (n = 10) compared with controls (n = 9).
** p < 0.01. (B): EL-NE fragment levels in serum from patients diagnosed with lung cancer (n = 40 in total), SCC (n = 16), adenocarcinoma (n = 16) and SCLC (n = 8) compared with controls (n = 12). **** p < 0.0001. Groups were compared by T-test with Welch correction. Data are shown as the geometric mean (95% CI).
Abbreviations: IPF, idiopathic pulmonary fibrosis; SCC, squamous cell carcinoma; SCLC, small cell lung carcinoma.
Sandwich ELISA - HRP Conjugation Kit - Lightning-Link® (ab102890)
HRP conjugation kit ab102890 is used by Abcam extensively in ELISA development. It is used for development / manufacturing of Abcam's SimpleStep ELISA® kits, including the Frataxin ELISA kit Human Frataxin ELISA Kit ab176112 used to produce the image above.
Transformed B lymphocyte cells from Friedreich's Ataxia (FA) samples were compared to heterozygous carrier B lymphocyte cells (Carrier) and control B lymphocyte cells (Control). B lymphocyte cell extracts were analyzed across a 7-point titration (0.1-100 μg/mL) and frataxin levels were interpolated from the standard curve. Average interpolated values of Frataxin are plotted.
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