http://www.mountsinai.org/Education/School%20of%20Medicine
home.html
sorianosoriano.htmlshapeimage_3_link_0
protocolssorianopro.htmlshapeimage_4_link_0
ES cell culturesorianoescc.htmlshapeimage_5_link_0
PCRsorianopcr.htmlshapeimage_6_link_0
ES screening by PCRsorianoespcr.htmlshapeimage_7_link_0
southern blotsorianoblot.htmlshapeimage_8_link_0
ES screening by southernssorianoess.htmlshapeimage_9_link_0
http://gallery.me.com/drbsinai#100039&bgcolor=black&view=mosaic&sel=0
 

Soriano Lab - Protocols

3sorianopro.html

X-gal Staining

    Fixative solution for embryos, embryo sections, and ES cells: 2% formaldehyde (from a 37% stock), and 0.2% glutaraldehyde (grade I, from a 25% stock) in PBS; make fresh for each use.  Fix on ice for following times:


Volumes are suitable for a litter of up to 12 embryos.

    Staining solution for embryos, embryo sections, and ES cells: 1 mg/ml X-Gal, 5 mM potassium ferricyanide, 5 mM potassium ferrocyanide, 2 mM MgCI, 0.01% sodium deoxycholate, and 0.02% Nonidet P-40 (NP-40) in PBS.  This solution, without X-Gal, can be prepared in advance and stored at room temperature in the dark.  Add X-Gal from a stock solution just before use.

    X-Gal (5 -Bromo-4-chloro-3-indolyl-beta-D-galactopyranoside) stock: 40 mg/ml in dimethylformamide; store at - 20 degrees in small aliquots and ensure that X-Gal is well dissolved before use otherwise crystals may form in the staining solution.

    Please note that for larger embryos (E11.5 and above) and adult tissues, there is very inefficient penetration of the X-Gal stain.  According to the tissue, penetration may be less than 1 mm.  In such cases, we have found the following method to be advantageous:

  1. 1.  Fix the embryo or tissue only for a short time.
    2.  Make 500 um-1mm sections using a vibratome.
    3.  Refix the tissue.
    4.  Stain with X-Gal as above.

Using such a protocol, we obtain uniform staining of tissues, for instance with ROSA26.