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AB102887

Glucose Oxidase Conjugation Kit - Lightning-Link®

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(9 제품이 사용된 논문 )

Glucose Oxidase Conjugation Kit - Lightning-Link® (ab102887) offers several standout features:

- Rapid Conjugation: achieve Glucose Oxidase (GOx) labeling in under 4 hours with just 30 seconds of hands-on time.
- High Efficiency: ensures 100% antibody recovery, meaning no loss of valuable antibodies.
- Versatility: suitable for conjugating antibodies, proteins, and peptides. GOx-labeled antibodies can be used immediately in applications such as Western blot, ELISA, and Immunohistochemistry (IHC) without further purification.
3 이미지
Schematic Diagram - Glucose Oxidase Conjugation Kit - Lightning-Link® (AB102887)
  • Schematic Diagram

Supplier Data

This illustration demonstrates a general procedure of how Lightning-Link® labeling technology enables the direct labeling of antibodies or proteins.

Simply pipette your antibody or biomolecule of choice into the vial of a lyophilized mixture containing the label of interest and incubate for around 3 hours. Please see the ab102887 protocol booklet for more details.

Learn more about our Lightning-Link® conjugation kits here

Other - Glucose Oxidase Conjugation Kit - Lightning-Link® (AB102887)
  • Other

Lab

Representative image of Glucose Oxidase Conjugation Kit - Lightning-Link® (ab102887)

Components shown from left to right :

Glucose Oxidase mix (1 vial for 100 µg, 1 mg)

Modifier reagent (1 vial)

Quencher reagent (1 vial)

Securitainer

Note : The vial labels shown in this image use generic names for illustrative purposes only and may not exactly match the specific component names included in the conjugation kit.

Note : Color of the lyophilized material in image may not precisely match the color shade in the actual kit.

Other - Glucose Oxidase Conjugation Kit - Lightning-Link® (AB102887)
  • Other

Lab

Representative image of Glucose Oxidase Conjugation Kit - Lightning-Link® (ab102887)

Components shown from left to right :

Glucose Oxidase mix (3 vials for 3x 10 µg, 3x 100 µg)

Modifier reagent (1 vial)

Quencher reagent (1 vial)

Securitainer

Note : The vial labels shown in this image use generic names for illustrative purposes only and may not exactly match the specific component names included in the conjugation kit.

Note : Color of the lyophilized material in image may not precisely match the color shade in the actual kit.

주요 정보

제품 세부 정보

Glucose Oxidase Conjugation Kit / Glucose Oxidase Labeling Kit ab102887 uses a simple and quick process for glucose oxidase labeling / conjugation of antibodies. It can also be used to conjugate other proteins or peptides. Learn about our . To conjugate an antibody to Glucose Oxidase using this kit: - add modifier to antibody and incubate for 3 hrs - add quencher and incubate for 30 mins The glucose oxidase 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 Glucose Oxidase. 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® GOx Labeling Kit. 706-0015 is the same as the 1 mg size. 706-0010 is the same as the 3 x 100 ug size. 706-0030 is the same as the 3 x 10 ug size.

Amount and volume of antibody for conjugation to Glucose Oxidase

Kit size Recommended maximum
amount of antibody
Maximum antibody
volume1
3 x 10 μg 3 x 10 μg 3 x 10 μL
3 x 100 μg 3 x 100 μg 3 x 100 μL
1 mg 1 x 1 mg 1 x 1 mL

1 Ideal antibody concentration is 1mg/ml. 0.5 - 1 mg/ml can be used if the maximum antibody volume is not exceeded. Antibodies > 1 mg/ml or < 0.5 mg/ml should be diluted /concentrated.

Buffer Requirements for Conjugation

Buffer should be pH 6.5-8.5.

Compatible buffer constituents
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.

50mM / 0.6% Tris1 0.1% BSA 50% glycerol
0.1% sodium azide PBS Potassium phosphate
Sodium chloride HEPES Sucrose
Sodium citrate EDTA Trehalose

1 Tris buffered saline is almost always ≤ 50 mM / 0.6%

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.

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.

제품 구성

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특성 및 보관 정보

배송 시 보관 조건
Ambient - Cannot Ship with Ice
적절한 단기 보관 조건
-20°C
적절한 장기 보관 조건
-20°C
보관 정보
-20°C

제품 프로토콜

타겟 정보

제품이 사용된 논문 (9)

Recent publications for all applications. Explore the 전체 목록 and refine your search

Biosensors 12: PubMed35323432

2022

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Yitao Liang,Bin Zhang,Zexin Xue,Xuesong Ye,Bo Liang

Sensors (Basel, Switzerland) 21: PubMed33670868

2021

Paper-Based Competitive Immunochromatography Coupled with an Enzyme-Modified Electrode to Enable the Wireless Monitoring and Electrochemical Sensing of Cotinine in Urine.

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Nutcha Larpant,Pramod K Kalambate,Tautgirdas Ruzgas,Wanida Laiwattanapaisal

Biosensors & bioelectronics 148:111824 PubMed31698303

2019

Impact of assay format on miRNA sensing: Electrochemical microfluidic biosensor for miRNA-197 detection.

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Hazal Kutluk,Richard Bruch,Gerald A Urban,Can Dincer

Advanced materials (Deerfield Beach, Fla.) 31:e1905311 PubMed31663165

2019

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Richard Bruch,Julia Baaske,Claire Chatelle,Mailin Meirich,Sibylle Madlener,Wilfried Weber,Can Dincer,Gerald Anton Urban

Biosensors & bioelectronics 126:102-107 PubMed30396016

2018

A bisulfite treatment and PCR-free global DNA methylation detection method using electrochemical enzymatic signal engagement.

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Ripon Bhattacharjee,Sofia Moriam,Nam-Trung Nguyen,Muhammad J A Shiddiky

Biosensors & bioelectronics 126:82-87 PubMed30396021

2018

Calorimetric sandwich-type immunosensor for quantification of TNF-α.

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Saif Mohammad Ishraq Bari,Louis G Reis,Gergana G Nestorova

Proceedings of the National Academy of Sciences of 113:6403-8 PubMed27217569

2016

Enzymatically enhanced collisions on ultramicroelectrodes for specific and rapid detection of individual viruses.

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Jeffrey E Dick,Adam T Hilterbrand,Lauren M Strawsine,Jason W Upton,Allen J Bard

Talanta 148:200-8 PubMed26653441

2015

Rapid detection of Escherichia coli O157:H7 and Salmonella Typhimurium in foods using an electrochemical immunosensor based on screen-printed interdigitated microelectrode and immunomagnetic separation.

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Meng Xu,Ronghui Wang,Yanbin Li

Analytical chemistry 85:4863-8 PubMed23663141

2013

Glucose-oxidase label-based redox cycling for an incubation period-free electrochemical immunosensor.

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Amardeep Singh,Seonhwa Park,Haesik Yang
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