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k ras2a  (Santa Cruz Biotechnology)


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    Structured Review

    Santa Cruz Biotechnology k ras2a
    K Ras2a, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 85/100, based on 6 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/k+ras2a/K-Ras-2A+Antibody/pm19372139-77-8-12
    Average 85 stars, based on 6 article reviews
    k ras2a - by Bioz Stars, 2026-10
    85/100 stars

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    Related Articles

    Saline:

    Article Title: The miR-18a* microRNA functions as a potential tumor suppressor by targeting on K-Ras.
    Article Snippet: Subsequently, the protein was resolved in 12% sodium dodecyl sulfate–polyacrylamide gel electrophoresis minigel and transferred onto the Immobilon-P membrane (Millipore, Billerica, MA). .. Membranes were probed with primary antibodies against pan-Ras, K-Ras2A, K-Ras2B and b-actin (Santa Cruz Biotechnology, Santa Cruz, CA) at room temperature for 2 h, washed extensively with 0.1% Tween-20 in phosphate-buffered saline and incubated with secondary antibodies conjugated with horse-radish peroxidase at 1:10 000 dilution. .. The signals were visualized with enhanced chemiluminescence (Amersham Life Science, Buckinghamshire, UK).

    Incubation:

    Article Title: The miR-18a* microRNA functions as a potential tumor suppressor by targeting on K-Ras.
    Article Snippet: Subsequently, the protein was resolved in 12% sodium dodecyl sulfate–polyacrylamide gel electrophoresis minigel and transferred onto the Immobilon-P membrane (Millipore, Billerica, MA). .. Membranes were probed with primary antibodies against pan-Ras, K-Ras2A, K-Ras2B and b-actin (Santa Cruz Biotechnology, Santa Cruz, CA) at room temperature for 2 h, washed extensively with 0.1% Tween-20 in phosphate-buffered saline and incubated with secondary antibodies conjugated with horse-radish peroxidase at 1:10 000 dilution. .. The signals were visualized with enhanced chemiluminescence (Amersham Life Science, Buckinghamshire, UK).



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    Santa Cruz Biotechnology polyclonal anti k ras2a antibody
    FIG. 1. In vitro translation of pKras2A produces a 21-kDa pro- tein. This autoradiograph of a gel containing the protein product of an in vitro translation reaction shows that pKras2A but not a negative control (control (CON) no plasmid) produces a protein of a size consist- ent with full-length <t>K-Ras2A</t> (;21 kDa).
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    FIG. 1. In vitro translation of pKras2A produces a 21-kDa pro- tein. This autoradiograph of a gel containing the protein product of an in vitro translation reaction shows that pKras2A but not a negative control (control (CON) no plasmid) produces a protein of a size consist- ent with full-length K-Ras2A (;21 kDa).

    Journal: The Journal of biological chemistry

    Article Title: Regulation of Na(+) reabsorption by the aldosterone-induced small G protein K-Ras2A.

    doi: 10.1074/jbc.274.50.35449

    Figure Lengend Snippet: FIG. 1. In vitro translation of pKras2A produces a 21-kDa pro- tein. This autoradiograph of a gel containing the protein product of an in vitro translation reaction shows that pKras2A but not a negative control (control (CON) no plasmid) produces a protein of a size consist- ent with full-length K-Ras2A (;21 kDa).

    Article Snippet: The polyclonal anti-K-Ras2A antibody (from Santa Cruz) was created against an epitope found only in the A splice variant of K-Ras: the A and B variants diverge at the C terminus between amino acids 165–184.

    Techniques: In Vitro, Autoradiography, Negative Control, Control, Plasmid Preparation

    FIG. 2. K-Ras2A is an aldosterone-induced protein. A, the left lane (control (CON)) of this Western blot probed with anti-K-Ras2A antibody contains protein from A6 cells not treated with aldosterone that was immunoprecipitated with anti-K-Ras antibody. The right lane (ALDO) contains protein immunoprecipitated from cells treated with aldosterone for 4 h. B, This graph summarizes six such experiments. All paired immunoprecipitants (lines) were performed on the same day and on lysates that contained the same amount of starting, total protein.

    Journal: The Journal of biological chemistry

    Article Title: Regulation of Na(+) reabsorption by the aldosterone-induced small G protein K-Ras2A.

    doi: 10.1074/jbc.274.50.35449

    Figure Lengend Snippet: FIG. 2. K-Ras2A is an aldosterone-induced protein. A, the left lane (control (CON)) of this Western blot probed with anti-K-Ras2A antibody contains protein from A6 cells not treated with aldosterone that was immunoprecipitated with anti-K-Ras antibody. The right lane (ALDO) contains protein immunoprecipitated from cells treated with aldosterone for 4 h. B, This graph summarizes six such experiments. All paired immunoprecipitants (lines) were performed on the same day and on lysates that contained the same amount of starting, total protein.

    Article Snippet: The polyclonal anti-K-Ras2A antibody (from Santa Cruz) was created against an epitope found only in the A splice variant of K-Ras: the A and B variants diverge at the C terminus between amino acids 165–184.

    Techniques: Control, Western Blot, Immunoprecipitation

    FIG. 3. K-Ras2A is necessary for aldosterone-stimulated Na1

    Journal: The Journal of biological chemistry

    Article Title: Regulation of Na(+) reabsorption by the aldosterone-induced small G protein K-Ras2A.

    doi: 10.1074/jbc.274.50.35449

    Figure Lengend Snippet: FIG. 3. K-Ras2A is necessary for aldosterone-stimulated Na1

    Article Snippet: The polyclonal anti-K-Ras2A antibody (from Santa Cruz) was created against an epitope found only in the A splice variant of K-Ras: the A and B variants diverge at the C terminus between amino acids 165–184.

    Techniques:

    FIG. 5. Overexpression of K-Ras2A in A6 cells increases Na1

    Journal: The Journal of biological chemistry

    Article Title: Regulation of Na(+) reabsorption by the aldosterone-induced small G protein K-Ras2A.

    doi: 10.1074/jbc.274.50.35449

    Figure Lengend Snippet: FIG. 5. Overexpression of K-Ras2A in A6 cells increases Na1

    Article Snippet: The polyclonal anti-K-Ras2A antibody (from Santa Cruz) was created against an epitope found only in the A splice variant of K-Ras: the A and B variants diverge at the C terminus between amino acids 165–184.

    Techniques: Over Expression

    FIG. 7. Aldosterone activates (phosphorylates) MEK 1/2 via K-Ras2A signaling. A these typical Western blots show that cells treated with aldosterone have more protein immunoreactive with anti- phospho-MEK 1/2 antibody compared with cells treated with vehicle (control (CON)). Each lane contains similar amounts of total protein. The time of aldosterone or vehicle treatment is indicated. Note, merely washing cells with vehicle sometimes (as in this figure) appeared to slightly increase phospho-MEK levels; however, this observation was not consistent (observed ;50% of the time). This inconsistent and slight increase in phospho-MEK upon washing results in only a little under- estimation of MEK activation by aldosterone. B, this typical Western blot shows that aldosterone activates MEK in sense (SENSE) but not antisense (ANTI) K-ras2A-treated cells. The top blots were probed with anti-phospho-MEK, and the bottom blots were probed with anti-MEK antibody. All lanes contained similar amounts of total protein.

    Journal: The Journal of biological chemistry

    Article Title: Regulation of Na(+) reabsorption by the aldosterone-induced small G protein K-Ras2A.

    doi: 10.1074/jbc.274.50.35449

    Figure Lengend Snippet: FIG. 7. Aldosterone activates (phosphorylates) MEK 1/2 via K-Ras2A signaling. A these typical Western blots show that cells treated with aldosterone have more protein immunoreactive with anti- phospho-MEK 1/2 antibody compared with cells treated with vehicle (control (CON)). Each lane contains similar amounts of total protein. The time of aldosterone or vehicle treatment is indicated. Note, merely washing cells with vehicle sometimes (as in this figure) appeared to slightly increase phospho-MEK levels; however, this observation was not consistent (observed ;50% of the time). This inconsistent and slight increase in phospho-MEK upon washing results in only a little under- estimation of MEK activation by aldosterone. B, this typical Western blot shows that aldosterone activates MEK in sense (SENSE) but not antisense (ANTI) K-ras2A-treated cells. The top blots were probed with anti-phospho-MEK, and the bottom blots were probed with anti-MEK antibody. All lanes contained similar amounts of total protein.

    Article Snippet: The polyclonal anti-K-Ras2A antibody (from Santa Cruz) was created against an epitope found only in the A splice variant of K-Ras: the A and B variants diverge at the C terminus between amino acids 165–184.

    Techniques: Western Blot, Control, Activation Assay

    FIG. 8. A possible model of aldosterone signal transduction. Our results support the idea that K-Ras2A synthesis in response to aldosterone is limiting in some instances for regulation of Na1 trans- port by this steroid. Note that the K-Ras2A and methylation signaling pathways, both of which are initiated by aldosterone, converge prior to activation of ENaC. However, other pathways not tested in this study also are likely to be involved in steroid-induction of Na1 reabsorption.

    Journal: The Journal of biological chemistry

    Article Title: Regulation of Na(+) reabsorption by the aldosterone-induced small G protein K-Ras2A.

    doi: 10.1074/jbc.274.50.35449

    Figure Lengend Snippet: FIG. 8. A possible model of aldosterone signal transduction. Our results support the idea that K-Ras2A synthesis in response to aldosterone is limiting in some instances for regulation of Na1 trans- port by this steroid. Note that the K-Ras2A and methylation signaling pathways, both of which are initiated by aldosterone, converge prior to activation of ENaC. However, other pathways not tested in this study also are likely to be involved in steroid-induction of Na1 reabsorption.

    Article Snippet: The polyclonal anti-K-Ras2A antibody (from Santa Cruz) was created against an epitope found only in the A splice variant of K-Ras: the A and B variants diverge at the C terminus between amino acids 165–184.

    Techniques: Transduction, Methylation, Protein-Protein interactions, Activation Assay