Overview

  • Product name

  • Tested applications

    Suitable for: WB, ELISA, SDS-PAGE, IPmore details
  • General notes

    Abcam’s 10X RIPA lysis buffer is an efficient means of cell lysis and protein solubilization for both adherent and suspension cultured mammalian cells. This reagent effectively extracts cytoplasmic, nuclear and membrane proteins. It is compatible with many downstream applications, including SDS-PAGE, Western blot, immunoprecipitation, ELISA and BCA assays.

    10X RIPA Buffer may precipitate when stored at + 4ºC. To dissolve crystals, warm briefly at + 37ºC and mix by inversion. After diluting to 1X bring solution to + 4ºC prior to extracting your samples.

Properties

  • Form

    Liquid
  • Storage instructions

    Store at +4°C.
  • Storage buffer

    pH: 7.50
    Constituents: 0.22% Beta glycerophosphate, 10% Tergitol-NP40, 0.18% Sodium orthovanadate, 5% Sodium deoxycholate, 0.38% EGTA, 1% SDS, 6.1% Tris, 0.29% EDTA, 8.8% Sodium chloride, 1.12% Sodium pyrophosphate decahydrate
  • Concentration information loading...
  • Research areas

Applications

Our Abpromise guarantee covers the use of ab156034 in the following tested applications.

The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.

Application Abreviews Notes
WB Use at an assay dependent concentration. Suggested working concentration: 1X
ELISA Use at an assay dependent concentration. Suggested working concentration: 1X
SDS-PAGE Use at an assay dependent concentration. Suggested working concentration: 1X
IP Use at an assay dependent concentration. Suggested working concentration: 1X

Images

  • HeLa cell extraction using ab156034.
    2.5 million HeLa cells were lysed on ice for 15 minutes with 0.5 mL of 1X ab156034. Next the sample was centrifuged at 14,000 rpm at 4ºC for 15 minutes: the supernatant ( = cleared lysate) was removed and the pellet ( = insoluble material) was resuspended in 0.5 mL lysis buffer and solubilized by sonication. Equivalent loads of the cleared lysate and solubilized pellet were analyzed by SDS-PAGE and Coomassie stain.
    BCA protein concentration determination of the soluble and insoluble material indicates that a total of 1.1mg of protein was recovered and 82% was in the soluble cleared cell lysate.

    Lane 1: MW marker
    Lane 2: Cleared lysate
    Lane 3: Non-soluble

References

This product has been referenced in:

  • Yang Q  et al. Overexpression of microRNA-101 causes anti-tumor effects by targeting CREB1 in colon cancer. Mol Med Rep 19:3159-3167 (2019). Read more (PubMed: 30816471) »
  • Kasai H  et al. Efficient siRNA delivery and gene silencing using a lipopolypeptide hybrid vector mediated by a caveolae-mediated and temperature-dependent endocytic pathway. J Nanobiotechnology 17:11 (2019). Read more (PubMed: 30670041) »
See all 38 Publications for this product

Customer reviews and Q&As

1-4 of 4 Abreviews or Q&A

quick and easy

Excellent Excellent 5/5 (Ease of Use)
Abreviews
We use the 10x RIPA buffer in the 1x concentration to extract proteins for the western blot.
It works very well to extract cytoplasmic, nuclear and membrane proteins. It's quick and easy.

Abcam user community

Verified customer

Submitted Apr 06 2018

Abreview for ab156034 - 10X RIPA Buffer

Good Excellent 5/5 (Ease of Use)
Abreviews
This 10X RIPA Buffer is very convenient to use.

Abcam user community

Verified customer

Submitted Aug 07 2015

Answer

Yes the 10x concentrated RIPA buffer (ab156034) should be diluted to a 1x concentration using distilled water.

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Question
Answer

Please use distilled water to dilute the 10X RIPA buffer. Thanks!

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Please note: All products are "FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC PROCEDURES"
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