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AB102907

PerCP Conjugation Kit - Lightning-Link®

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(7 제품이 사용된 논문 )

PerCP Conjugation Kit - Lightning-Link® (ab102907) offers several standout features:

- Rapid Conjugation: achieve PerCP 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. PerCP labeled antibodies can be used immediately in applications such as Western blot (WB), ELISA, and Immunohistochemistry (IHC) without further purification.
3 이미지
Schematic Diagram - PerCP Conjugation Kit - Lightning-Link® (AB102907)
  • 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 ab102907 protocol booklet for more details.

Learn more about our Lightning-Link® conjugation kits here

Other - PerCP Conjugation Kit - Lightning-Link® (AB102907)
  • Other

Lab

Representative image of PerCP Conjugation Kit - Lightning-Link® (ab102907)

Components shown from left to right :

PerCP 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.

Other - PerCP Conjugation Kit - Lightning-Link® (AB102907)
  • Other

Lab

Representative image of PerCP Conjugation Kit - Lightning-Link® (ab102907)

Components shown from left to right :

PerCP 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.

주요 정보

제품 세부 정보

PerCP Conjugation Kit - Lightning-Link® (ab102907) uses a simple and quick process for labeling / conjugation of antibodies. It can also be used to conjugate other proteins or peptides.

To conjugate an antibody to PerCP using this kit:
- add modifier to antibody and incubate for 3 hrs
- add quencher and incubate for 30 min

The PerCP conjugated antibody can be used immediately in Flow cytometry, WB, ELISA, IHC etc. No further purification is required and 100% of the antibody is recovered for use.

Learn about our antibody labeling kits and their advantages here.

Learn about buffer compatibility below; for incompatible buffers and low antibody concentrations, use our antibody purification and concentration kits.
Custom size conjugation kits up to 100 mg are available on demand. Please contact us to discuss your requirements.

Amount and volume of antibody for conjugation to PerCP

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

This product is manufactured by Expedeon, an Abcam company, and was previously called Lightning-Link® PerCP Labeling Kit. 718-0015 is the same as the 1 mg size. 718-0010 is the same as the 3 x 100 µg size. 718-0030 is the same as the 3 x 10 µg size. 718-0005 is the same as the 100 µg size.

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 (7)

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

Veterinary and comparative oncology 20:427-436 PubMed34797014

2021

Evaluation of lymphocyte-specific programmed cell death protein 1 receptor expression and cytokines in blood and urine in canine urothelial carcinoma patients.

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Christopher J Pinard,Ashley A Stegelmeier,Byram W Bridle,Anthony J Mutsaers,R Darren Wood,Geoffrey A Wood,J Paul Woods,Samuel E Hocker

Scientific reports 10:18848 PubMed33139767

2020

Hepatobiliary malignancies have distinct peripheral myeloid-derived suppressor cell signatures and tumor myeloid cell profiles.

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Defne Bayik,Adam J Lauko,Gustavo A Roversi,Emily Serbinowski,Lou-Anne Acevedo-Moreno,Christopher Lanigan,Mushfig Orujov,Alice Lo,Tyler J Alban,Adam Kim,Daniel J Silver,Laura E Nagy,J Mark Brown,Daniela S Allende,Federico N Aucejo,Justin D Lathia

Nature neuroscience 23:771-781 PubMed32341540

2020

Single-nucleus transcriptomics of the prefrontal cortex in major depressive disorder implicates oligodendrocyte precursor cells and excitatory neurons.

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Corina Nagy,Malosree Maitra,Arnaud Tanti,Matthew Suderman,Jean-Francois Théroux,Maria Antonietta Davoli,Kelly Perlman,Volodymyr Yerko,Yu Chang Wang,Shreejoy J Tripathy,Paul Pavlidis,Naguib Mechawar,Jiannis Ragoussis,Gustavo Turecki

Translational research : the journal of laboratory 172:73-83.e1 PubMed27012475

2016

Circulating fibrocytes as predictors of adverse events in unstable angina.

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Ellen C Keeley,Robert C Schutt,Mark A Marinescu,Marie D Burdick,Robert M Strieter,Borna Mehrad

Avian pathology : journal of the W.V.P.A 44:452-62 PubMed26305169

2015

In vitro characterization of chicken bone marrow-derived dendritic cells following infection with very virulent infectious bursal disease virus.

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A R Yasmin,S K Yeap,S W Tan,M Hair-Bejo,S Fakurazi,P Kaiser,A R Omar

Biomedical optics express 6:3303-12 PubMed26417502

2015

In vivo imaging of activated microglia in a mouse model of focal cerebral ischemia by two-photon microscopy.

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Seoyeon Bok,Taejun Wang,Chan-Ju Lee,Seong-Uk Jeon,Young-Eun Kim,Jeongwoo Kim,Beom-Ju Hong,Calvin Jinse Yoon,Sungjee Kim,Seung-Hoon Lee,Hak Jae Kim,Il Han Kim,Ki Hean Kim,G-One Ahn

Glia 63:768-79 PubMed25557204

2015

IL-17A activates ERK1/2 and enhances differentiation of oligodendrocyte progenitor cells.

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Jane M Rodgers,Andrew P Robinson,Elen S Rosler,Karen Lariosa-Willingham,Rachael E Persons,Jason C Dugas,Stephen D Miller
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