For western blots, incubate membrane with diluted primary antibody in 5% w/v BSA, 1X TBS, 0.1% Tween® 20 at 4°C with gentle shaking, overnight.
NOTE: Please refer to primary antibody datasheet or product webpage for recommended antibody dilution.
From sample preparation to detection, the reagents you need for your Western Blot are now in one convenient kit: #12957 Western Blotting Application Solutions Kit
NOTE: Prepare solutions with reverse osmosis deionized (RODI) or equivalent grade water.
Load 20 µl onto SDS-PAGE gel (10 cm x 10 cm).
NOTE: Volumes are for 10 cm x 10 cm (100 cm2) of membrane; for different sized membranes, adjust volumes accordingly.
* Avoid repeated exposure to skin.
posted June 2005
revised November 2013
Reprobing of an existing membrane is a convenient means to immunoblot for multiple proteins independently when only a limited amount of sample is available. It should be noted that for the best possible results a fresh blot is always recommended. Reprobing can be a valuable method but with each reprobing of a blot there is potential for increased background signal. Additionally, it is recommended that you verify the removal of the first antibody complex prior to reprobing so that signal attributed to binding of the new antibody is not leftover signal from the first immunoblotting experiment. This can be done by re-exposing the blot to ECL reagents and making sure there is no signal prior to adding the next primary antibody.
NOTE: Prepare solutions with reverse osmosis deionized (RODI) or equivalently purified water.
posted June 2005
revised October 2016
Protocol Id: 10
Supplied in 10 mM sodium HEPES (pH 7.5), 150 mM NaCl, 100 µg/ml BSA, 50% glycerol and less than 0.02% sodium azide. Store at –20°C. Do not aliquot the antibody.
E-Ras (D5G5J) Rabbit mAb recognizes endogenous levels of total mouse E-Ras protein. It recognizes transfected levels of human E-Ras protein. This antibody does not cross-react with human H-, K-, N-, or R-Ras proteins.
Monoclonal antibody is produced by immunizing animals with a synthetic peptide corresponding to residues surrounding Ala30 of human E-Ras protein.
E-Ras (Embryonic Ras) is a member of the Ras family that includes K-Ras, N-Ras, and H-Ras. E-Ras is expressed in early mouse blastocysts and murine embryonic stem cells and is down-regulated upon differentiation (1). Amino acid substitutions as a result of mutation at three conserved positions in K-, H-, N-, and R-Ras proteins result in constitutive activation of these small GTPases, and oncogenic transformation. Intriguingly, the Eras gene encodes a protein where each of these amino acids are substituted, and so E-Ras is naturally constitutively active. E-Ras is thought to contribute to the tumorigenic potential of mouse ES cells to form teratomas in immunodeficient or isogenic mice (1). Despite the parallels between oncogenic mutated Ras, major differences in signaling exist between H-Ras G12V and E-Ras. While H-Ras G12V highly activates the MAPK pathway, E-Ras cannot bind to Raf1 to activate this pathway. Instead, E-Ras signals through PI3K to activate Akt (1). E-Ras is not expressed in human embryonic stem cells, nor is it is expressed in any adult tissues as found thus far (2). Reports have suggested it may be expressed in several tumor types, including gastric cancer (1,2,3). Researchers have speculated on the role of E-Ras in the early mouse blastocyst. Preimplantation embryos can survive in tissue culture in defined medium until the blastocyst stage without any requirement for serum or growth factors. Preimplantation embryos have a requirement for PI3K signaling, and in the absence of exogenous signals, E-Ras has been suggested to be the effector of this signal transduction (6).
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|12575S||100 µl (10 western blots)||$ 255.0|