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ProLite™ His-Tag Protein Gel Staining Kit *Green Fluorescence*

The polyhistidine tag (His-Tag) is widely used for protein purification, detection, and immobilization. The ProLite™ His-Tag Protein Gel Staining Kit provides a fast, sensitive, and highly specific fluorescent stain for visualizing His-tagged fusion proteins directly in a polyacrylamide gel following electrophoresis. This kit requires very little hands-on time, allowing for rapid protein expression screening in a variety of gel types using an imaging equipment with a standard FITC filter. It detects nanogram of His-tagged proteins directly in gels, thus eliminating the additional western blotting step. AAT Bioquest offers the largest selection of the His-Tag detection and purification products.

Example protocol

PREPARATION OF STOCK SOLUTIONS

Unless otherwise noted, all unused stock solutions should be divided into single-use aliquots and stored at -20 °C after preparation. Avoid repeated freeze-thaw cycles.

ProLite™ His-Tag Protein Gel Stain stock solution
Prepare a ProLite™ His-Tag Protein Gel Stain stock solution by adding  60 µL of DMSO to a vial of ProLite™ His-Tag Protein Gel Stain. Note: 1 vial of stock solution is suitable for two gels. Store any unused stock solution at -20 °C.

PREPARATION OF WORKING SOLUTION

ProLite™ His Tag Protein Gel Stain working solution
Prepare a ProLite™ His-Tag Protein Gel Stain working solution by adding 30 µL of ProLite™ His-Tag Protein Gel Stain stock solution to 30 mL of PBS. Note: Make enough working solution that the gel is completely immersed in the working solution. Do not reuse the working solution.

SAMPLE EXPERIMENTAL PROTOCOL

The following protocol should be used as a guideline.

Post-staining protocol
  1. Run gels based on your standard protocol.
  2. Place the gel in a suitable container, and fix the gel in a fixing solution for 60 minutes. Note: 40% ethanol + 10% acetic acid can be used as a fixing solution.
  3. Wash the gel twice with ultra-pure water.
  4. Incubate the gel in the ProLite™ His-Tag Protein Gel Stain working solution for 60 minutes. Be sure the gel is immersed in the working solution.
  5. Remove the working solution and wash the gel twice with PBS.
  6. Proceed to imaging the gel immediately. 

Spectrum

References

View all 43 references: Citation Explorer
Simplified detection of polyhistidine-tagged proteins in gels and membranes using a UV-excitable dye and a multiple chelator head pair.
Authors: Raducanu, Vlad-Stefan and Isaioglou, Ioannis and Raducanu, Daniela-Violeta and Merzaban, Jasmeen S and Hamdan, Samir M
Journal: The Journal of biological chemistry (2020): 12214-12223
A bispecific circular aptamer tethering a built-in universal molecular tag for functional protein delivery.
Authors: Pan, Xiaoshu and Yang, Yu and Li, Long and Li, Xiaowei and Li, Qiang and Cui, Cheng and Wang, Bang and Kuai, Hailan and Jiang, Jianhui and Tan, Weihong
Journal: Chemical science (2020): 9648-9654
The surface syndecan protein from Macrobrachium rosenbergii could function as mediator in bacterial infections.
Authors: Yang, Hui and Xiong, Haoran and Mi, Kaihang and Zhang, Yingying and Zhang, Xiaojun and Chen, Guohong
Journal: Fish & shellfish immunology (2020): 62-68
[Cloning and expression of SmDXS2 gene in Swertia mussotii].
Authors: Li, Wen-Jing and Xiang, Bei-Bei and Sun, Yan-Xiang and Hou, Xiao-Qiang and Han, Mei-Ling and Li, Xiao-Xue and Wang, Yong and Guo, Shuo
Journal: Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica (2019): 935-941
Overexpression, Purification and Functional Characterisation of Wild-Type HIV-1 Subtype C Protease and Two Variants Using a Thioredoxin and His-Tag Protein Fusion System.
Authors: Zondagh, Jake and Williams, Alison and Achilonu, Ikechukwu and Dirr, Heini W and Sayed, Yasien
Journal: The protein journal (2018): 369-379
Page updated on December 17, 2024

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Catalog Number18010
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Physical properties

Solvent

DMSO

Spectral properties

Absorbance (nm)

487

Correction Factor (260 nm)

0.32

Correction Factor (280 nm)

0.35

Extinction coefficient (cm -1 M -1)

800001

Excitation (nm)

498

Emission (nm)

517

Quantum yield

0.79001, 0.952

Storage, safety and handling

H-phraseH303, H313, H333
Hazard symbolXN
Intended useResearch Use Only (RUO)
R-phraseR20, R21, R22

Storage

Freeze (< -15 °C); Minimize light exposure
UNSPSC12171501

Platform

Gel Imager

ExcitationBlue laser
EmissionLong path green filter (SYBR filter)
Two-fold dilution series of&nbsp;His-tagged annexin V were separated on a NuPAGE&reg; 4&ndash;12% Bis-Tris gel and stained with the ProLite&trade; His-Tag Protein Gel Staining Kit according to standard protocols. <strong>Lane 1:</strong> His-tagged protein ladder, <strong>Lane 2 to 5:</strong>&nbsp;two-fold dilution of His-tagged annexin V.
Two-fold dilution series of&nbsp;His-tagged annexin V were separated on a NuPAGE&reg; 4&ndash;12% Bis-Tris gel and stained with the ProLite&trade; His-Tag Protein Gel Staining Kit according to standard protocols. <strong>Lane 1:</strong> His-tagged protein ladder, <strong>Lane 2 to 5:</strong>&nbsp;two-fold dilution of His-tagged annexin V.
Two-fold dilution series of&nbsp;His-tagged annexin V were separated on a NuPAGE&reg; 4&ndash;12% Bis-Tris gel and stained with the ProLite&trade; His-Tag Protein Gel Staining Kit according to standard protocols. <strong>Lane 1:</strong> His-tagged protein ladder, <strong>Lane 2 to 5:</strong>&nbsp;two-fold dilution of His-tagged annexin V.