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SNAP2MINI

Millipore

SNAP id® 2.0 Protein Detection System-Mini

7.5 x 8.4 cm, Unique vacuum-driven technology & a built-in flow distributor actively drive reagents through the membrane

Synonym(s):

Protein detection kit

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About This Item

UNSPSC Code:
41116010
eCl@ss:
42029053
NACRES:
NB.22

product name

SNAP id® 2.0 Protein Detection System-Mini (7.5 x 8.4 cm), Developed to meet the needs of our Western blotting customers, the SNAP i.d. 2.0 system produces blots of a very high quality. Unique vacuum-driven technology & a built-in flow distributor actively drive reagents through the membrane..

manufacturer/tradename

SNAP id®

technique(s)

western blot: suitable

compatibility

for use with Commercially available blocking reagents
for use with Luminata Western HRP Substrates
for use with Nitrocellulose
for use with PVDF (Immobilon membranes)
for use with blØk<TMSYMBOL></TMSYMBOL>-CH Buffer (cat. no. WBAVDCH01)
for use with blØk<TMSYMBOL></TMSYMBOL>-FL Buffer (cat. no. WBAVDFL01)
for use with blØk<TMSYMBOL></TMSYMBOL>-PO Buffer (cat. no. WBAVDP001)
for use with commercially available detection reagents

detection method

chemiluminescent
colorimetric
fluorometric

shipped in

ambient

storage temp.

room temp

General description

The newly developed SNAP id 2.0 Protein Detection System is the second generation of the SNAP i.d. method for detecting immunoreactive proteins on western blots. With this unique vacuum-driven system, the length of time required for immunodetection is greatly reduced. The classical western blotting time frame of 4- 24 hours is now accomplished in 30 minutes with no quality and signal compromisation. All immunodetection steps after protein transfer to a membrane (i.e., blocking, washing, and primary and secondary antibody incubations) can be performed with the SNAP id 2.0 system. SNAP id 2.0 Mini Blot Holder accepts up to 7.5 × 8.4 cm blots.

Application

SNAP id 2.0 Protein Detection System-Mini (7.5 x 8.4 cm) has been used in western blot analysis.

Features and Benefits

SNAP id 2.0 Protein Detection System Features:
  • Processing of up to four blots at a time on a vacuum base with two individually controlled sides
  • Comprises of three removable blot holding frame sizes: MultiBlot, Mini, and Midi, to accommodate different blot sizes
  • Disposable blot holders, sized for MultiBlot, Mini, and Midi frames
  • Blot spacer required with first-generation SNAP id system is now integrated into the new blot holder
  • Extended and off-line blot processing options: frames have lids and can be removed from the base for extended incubation (one hour to overnight), incubation in a shaker, or incubation at 4 °C
  • Stackable frames so multiple blots can be processed at the same time;30-minute immunodetection with uniform signal across the blot
  • Greater than 80% antibody recovery using the SNAP id 2.0 Antibody Collection Trays
  • Compatible with nitrocellulose and polyvinylidene fluoride (PVDF) membranes
  • Works with the most blocking buffers and visualization methodologies (e.g. chemiluminescence, fluorescence, or colorimetric)

Packaging

This system includes the SNAP i.d.® 2.0 Base, two Mini Blot Holding Frames, two Antibody Collection Trays, vacuum tubing, Rolling Pad & Blot Roller, two Wetting Trays and a Quick Start Guide

Linkage

Replaces: WBAVDBASE

Other Notes

The SNAP i.d.® 2.0 Protein Detection System is intended for research use only. It is not for use in diagnostic procedures.

Legal Information

SNAP id is a registered trademark of Merck KGaA, Darmstadt, Germany

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Articles

Explore the impact of water quality on protein electrophoresis and Western blotting. Learn about the role of ultrapure water and its effect on chemiluminescent signals in Western blotting.

Protocols

The SNAP i.d. 2.0 Protein Detection System is the second generation of the SNAP i.d. method for detecting immunoreactive proteins on Western blots.

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

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