Vector VIP Substrate Kit, Peroxidase (HRP)

The Vector VIP HRP substrate produces an intense, violet (purple) reaction product, and can be used as an alternative to DAB or as a second color for multiple antigen labeling.

Features:

• Greater sensitivity than conventional substrates
• Consistent and reliable
• Ideal for IHC/ICC/ISH and blots
• Permanent mounting
• Stock solutions supplied in convenient dropper bottles promoting ease of handling
• No wait times for mixing and dissolving powders or tablets
• Sufficient reagents to produce 300 ml of working solution

$195.00

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SKU: SK-4600
Chromogen Color
Purple
Detection Enzyme
Peroxidase
Microscopy
Brightfield, Darkfield, Electron, Spectral Imaging
Mounting Medium Type
Non-Aqueous (Permanent)
Unit Size
1 Kit
Applications
Immunohistochemistry / Immunocytochemistry, In situ hybridization, Blotting Applications, Elispot
Additional Substrate Properties
Contrast with Tissue Pigments, Multiple Labeling
Substrate Reaction Product
Precipitating Reaction Product
Kit Components
  • 7 ml Vector VIP Reagent 1
  • 5 ml Vector VIP Reagent 2
  • 5 ml Vector VIP Reagent 3
  • 7.2 ml Vector VIP Reagent 4
Technical Information

Vector VIP and ImmPACT VIP chromogens also provide excellent color contrast in pigmented tissues such as melanoma or retina (1). Sections stained with either substrate can be viewed by darkfield and electron microscopy. Vector VIP and ImmPACT VIP substrates can be used for both manual and automated staining methods. Stained sections should be dehydrated, cleared, and permanently mounted.

Vector VIP Substrate Kit contains stock solutions in convenient dropper bottles. The sensitivity of Vector VIP substrate is equivalent to Vector DAB Substrate. This product can also be used on blots. The kit provides all of the necessary reagents to prepare about 300 ml of working solution. When stored at 4° C, this kit is stable for one year.

Product review on Biocompare.com.

1. Duncan SM, Seigel GM. High-contrast enzymatic immunohistochemistry of pigmented tissues. J Biol Methods2016;3(3):e47. doi: 10.14440/jbm.2016.122

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