anti fas ligand antibody  (Santa Cruz Biotechnology)

 
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    Santa Cruz Biotechnology anti fas ligand antibody
    Anti Fas Ligand Antibody, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    anti fas l mab nok 1  (Santa Cruz Biotechnology)

     
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    Santa Cruz Biotechnology anti fas l mab nok 1
    Anti Fas L Mab Nok 1, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    fas ligand mediated killing  (Santa Cruz Biotechnology)

     
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    Santa Cruz Biotechnology fas ligand mediated killing
    Fas Ligand Mediated Killing, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    fas l  (Santa Cruz Biotechnology)

     
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    Santa Cruz Biotechnology fas l
    Fas L, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    fas l  (Santa Cruz Biotechnology)

     
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    Santa Cruz Biotechnology fas l
    Mean ± standard deviation of fluorescent intensity measurements in corneal and Conjunctival epithelia stained for CD25, <t>CD122,</t> <t>MMP-9</t> in nonstressed (NS) C57BL/6 (A) or BKO and WT (B) and mice subjected for desiccating stress for 5 days (DS5) . A separate group of DS5 mice were topically treated with doxycycline (DS5+Doxy) (C) Mean ± standard deviation of fluorescent intensity measurements in corneal and conjunctival epithelia stained for <t>Fas-L</t> in nonstressed (NS) C57BL/6 mice (B6-NS), desiccating stressed C57BL/6 mice for 5 days (B6-DS5), NS C57BL/6 mice treated with bovine serum albumin (injection control, B6-NS+BSA) or IL-2 subconjunctival injections (B6-NS+IL-2), CD25 knock-out mice (CD25KO-NS). *P < 0.05; ** = P < 0.01; *** = P < 0.001.
    Fas L, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    1) Product Images from "Cleavage of functional IL-2 receptor alpha chain (CD25) from murine corneal and conjunctival epithelia by MMP-9"

    Article Title: Cleavage of functional IL-2 receptor alpha chain (CD25) from murine corneal and conjunctival epithelia by MMP-9

    Journal: Journal of Inflammation (London, England)

    doi: 10.1186/1476-9255-6-31

    Mean ± standard deviation of fluorescent intensity measurements in corneal and Conjunctival epithelia stained for CD25, CD122, MMP-9 in nonstressed (NS) C57BL/6 (A) or BKO and WT (B) and mice subjected for desiccating stress for 5 days (DS5) . A separate group of DS5 mice were topically treated with doxycycline (DS5+Doxy) (C) Mean ± standard deviation of fluorescent intensity measurements in corneal and conjunctival epithelia stained for Fas-L in nonstressed (NS) C57BL/6 mice (B6-NS), desiccating stressed C57BL/6 mice for 5 days (B6-DS5), NS C57BL/6 mice treated with bovine serum albumin (injection control, B6-NS+BSA) or IL-2 subconjunctival injections (B6-NS+IL-2), CD25 knock-out mice (CD25KO-NS). *P < 0.05; ** = P < 0.01; *** = P < 0.001.
    Figure Legend Snippet: Mean ± standard deviation of fluorescent intensity measurements in corneal and Conjunctival epithelia stained for CD25, CD122, MMP-9 in nonstressed (NS) C57BL/6 (A) or BKO and WT (B) and mice subjected for desiccating stress for 5 days (DS5) . A separate group of DS5 mice were topically treated with doxycycline (DS5+Doxy) (C) Mean ± standard deviation of fluorescent intensity measurements in corneal and conjunctival epithelia stained for Fas-L in nonstressed (NS) C57BL/6 mice (B6-NS), desiccating stressed C57BL/6 mice for 5 days (B6-DS5), NS C57BL/6 mice treated with bovine serum albumin (injection control, B6-NS+BSA) or IL-2 subconjunctival injections (B6-NS+IL-2), CD25 knock-out mice (CD25KO-NS). *P < 0.05; ** = P < 0.01; *** = P < 0.001.

    Techniques Used: Standard Deviation, Staining, Injection, Knock-Out

    fas ligand fasl  (Santa Cruz Biotechnology)

     
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    Santa Cruz Biotechnology fas ligand fasl
    Fas Ligand Fasl, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    anti fas l  (Santa Cruz Biotechnology)

     
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    Santa Cruz Biotechnology anti fas l
    Anti Fas L, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    fas ligand  (Santa Cruz Biotechnology)

     
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    Santa Cruz Biotechnology fas ligand
    Fas Ligand, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    anti fasl monoclonal antibody  (Santa Cruz Biotechnology)

     
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    Santa Cruz Biotechnology anti fasl monoclonal antibody
    a. <t>Positive</t> <t>FAS</t> expression; b. Positive <t>FASL</t> expression; c. Negative immunostaining. Magnification was 400×.
    Anti Fasl Monoclonal Antibody, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/anti fasl monoclonal antibody/product/Santa Cruz Biotechnology
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    1) Product Images from "FAS/FASL Expression Profile as a Prognostic Marker in Squamous Cell Carcinoma of the Oral Cavity"

    Article Title: FAS/FASL Expression Profile as a Prognostic Marker in Squamous Cell Carcinoma of the Oral Cavity

    Journal: PLoS ONE

    doi: 10.1371/journal.pone.0069024

    a. Positive FAS expression; b. Positive FASL expression; c. Negative immunostaining. Magnification was 400×.
    Figure Legend Snippet: a. Positive FAS expression; b. Positive FASL expression; c. Negative immunostaining. Magnification was 400×.

    Techniques Used: Expressing, Immunostaining

    a. and b.: Disease-free survival and disease-specific survival according to FAS expression; c. and d.: Disease-free survival and disease-specific survival according to FASL expression.
    Figure Legend Snippet: a. and b.: Disease-free survival and disease-specific survival according to FAS expression; c. and d.: Disease-free survival and disease-specific survival according to FASL expression.

    Techniques Used: Expressing

    a. and b.: Disease-free survival and disease-specific survival according to FAS/FASL profile.
    Figure Legend Snippet: a. and b.: Disease-free survival and disease-specific survival according to FAS/FASL profile.

    Techniques Used:

    fas l  (Santa Cruz Biotechnology)

     
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    Santa Cruz Biotechnology fas l
    Characterizion of the effects of Rm-HE on apoptotic signaling mediators. (A) Effect of Rm-HE on the expression and cleavage of apoptosis-related proteins in Jurkat cells. Expression of the anti-apoptotic proteins Bcl-XL, Mcl- 1 and Bcl-2 was analyzed in extracts of Jurkat cells treated as indicated by immunoblot with specific antibodies. Tubulin was used as an internal control. (B) Expression of pro-apoptotic proteins Bim, Bax and Bad was analyzed in extracts of Jurkat cells treated as indicated by immunoblot with specific antibodies. Tubulin was used as an internal control. (C) Fas Ligand induction was analyzed in extracts of Jurkat cells treated as indicated by immunoblot with specific antibodies. Tubulin was used as an internal control. (D) Statistical analysis for <t>Fas-L</t> expression blots in Rm-HE treated cells. Results indicate the average fold increase ± S.E.M in Fas-L expression relative to untreated cells from three independent experiments. The difference between untreated cells and cells treated for 16 h with Rm-HE are statistically significant (Student’s t -test: ** P < 0.01). (E) Effect of Rm-HE on Jurkat cell viability in the presence of <t>a</t> <t>JNK</t> inhibitor. Jurkat cells were pre-incubated for 1 h with 10μMSP600125 and then 40 μg/ml of Rm-HE were added for 24 h and 48 h, as indicated. Cell viability is represented as a percentage relative to untreated cells. Data is means ± S.E.M. from three independent determinations performed in duplicate. (F) Effect of Rm-HE on the JNK phosphorylation in Jurkat cells. Expression of JNK and phospho-JNK were analyzed in extracts of Jurkat cells treated as indicated by immunoblot with specific antibodies. Tubulin was used as an internal control.
    Fas L, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/fas l/product/Santa Cruz Biotechnology
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    1) Product Images from "Retama monosperma n -hexane extract induces cell cycle arrest and extrinsic pathway-dependent apoptosis in Jurkat cells"

    Article Title: Retama monosperma n -hexane extract induces cell cycle arrest and extrinsic pathway-dependent apoptosis in Jurkat cells

    Journal: BMC Complementary and Alternative Medicine

    doi: 10.1186/1472-6882-14-38

    Characterizion of the effects of Rm-HE on apoptotic signaling mediators. (A) Effect of Rm-HE on the expression and cleavage of apoptosis-related proteins in Jurkat cells. Expression of the anti-apoptotic proteins Bcl-XL, Mcl- 1 and Bcl-2 was analyzed in extracts of Jurkat cells treated as indicated by immunoblot with specific antibodies. Tubulin was used as an internal control. (B) Expression of pro-apoptotic proteins Bim, Bax and Bad was analyzed in extracts of Jurkat cells treated as indicated by immunoblot with specific antibodies. Tubulin was used as an internal control. (C) Fas Ligand induction was analyzed in extracts of Jurkat cells treated as indicated by immunoblot with specific antibodies. Tubulin was used as an internal control. (D) Statistical analysis for Fas-L expression blots in Rm-HE treated cells. Results indicate the average fold increase ± S.E.M in Fas-L expression relative to untreated cells from three independent experiments. The difference between untreated cells and cells treated for 16 h with Rm-HE are statistically significant (Student’s t -test: ** P < 0.01). (E) Effect of Rm-HE on Jurkat cell viability in the presence of a JNK inhibitor. Jurkat cells were pre-incubated for 1 h with 10μMSP600125 and then 40 μg/ml of Rm-HE were added for 24 h and 48 h, as indicated. Cell viability is represented as a percentage relative to untreated cells. Data is means ± S.E.M. from three independent determinations performed in duplicate. (F) Effect of Rm-HE on the JNK phosphorylation in Jurkat cells. Expression of JNK and phospho-JNK were analyzed in extracts of Jurkat cells treated as indicated by immunoblot with specific antibodies. Tubulin was used as an internal control.
    Figure Legend Snippet: Characterizion of the effects of Rm-HE on apoptotic signaling mediators. (A) Effect of Rm-HE on the expression and cleavage of apoptosis-related proteins in Jurkat cells. Expression of the anti-apoptotic proteins Bcl-XL, Mcl- 1 and Bcl-2 was analyzed in extracts of Jurkat cells treated as indicated by immunoblot with specific antibodies. Tubulin was used as an internal control. (B) Expression of pro-apoptotic proteins Bim, Bax and Bad was analyzed in extracts of Jurkat cells treated as indicated by immunoblot with specific antibodies. Tubulin was used as an internal control. (C) Fas Ligand induction was analyzed in extracts of Jurkat cells treated as indicated by immunoblot with specific antibodies. Tubulin was used as an internal control. (D) Statistical analysis for Fas-L expression blots in Rm-HE treated cells. Results indicate the average fold increase ± S.E.M in Fas-L expression relative to untreated cells from three independent experiments. The difference between untreated cells and cells treated for 16 h with Rm-HE are statistically significant (Student’s t -test: ** P < 0.01). (E) Effect of Rm-HE on Jurkat cell viability in the presence of a JNK inhibitor. Jurkat cells were pre-incubated for 1 h with 10μMSP600125 and then 40 μg/ml of Rm-HE were added for 24 h and 48 h, as indicated. Cell viability is represented as a percentage relative to untreated cells. Data is means ± S.E.M. from three independent determinations performed in duplicate. (F) Effect of Rm-HE on the JNK phosphorylation in Jurkat cells. Expression of JNK and phospho-JNK were analyzed in extracts of Jurkat cells treated as indicated by immunoblot with specific antibodies. Tubulin was used as an internal control.

    Techniques Used: Expressing, Western Blot, Incubation

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    a. Positive FAS expression; b. Positive FASL expression; c. Negative immunostaining. Magnification was 400×.

    Journal: PLoS ONE

    Article Title: FAS/FASL Expression Profile as a Prognostic Marker in Squamous Cell Carcinoma of the Oral Cavity

    doi: 10.1371/journal.pone.0069024

    Figure Lengend Snippet: a. Positive FAS expression; b. Positive FASL expression; c. Negative immunostaining. Magnification was 400×.

    Article Snippet: Anti-FAS monoclonal antibody and anti-FASL monoclonal antibody (Santa Cruz Biotechnology®, USA) were used in the IHC reaction, at a 1∶400 dilution – .

    Techniques: Expressing, Immunostaining

    a. and b.: Disease-free survival and disease-specific survival according to FAS expression; c. and d.: Disease-free survival and disease-specific survival according to FASL expression.

    Journal: PLoS ONE

    Article Title: FAS/FASL Expression Profile as a Prognostic Marker in Squamous Cell Carcinoma of the Oral Cavity

    doi: 10.1371/journal.pone.0069024

    Figure Lengend Snippet: a. and b.: Disease-free survival and disease-specific survival according to FAS expression; c. and d.: Disease-free survival and disease-specific survival according to FASL expression.

    Article Snippet: Anti-FAS monoclonal antibody and anti-FASL monoclonal antibody (Santa Cruz Biotechnology®, USA) were used in the IHC reaction, at a 1∶400 dilution – .

    Techniques: Expressing

    a. and b.: Disease-free survival and disease-specific survival according to FAS/FASL profile.

    Journal: PLoS ONE

    Article Title: FAS/FASL Expression Profile as a Prognostic Marker in Squamous Cell Carcinoma of the Oral Cavity

    doi: 10.1371/journal.pone.0069024

    Figure Lengend Snippet: a. and b.: Disease-free survival and disease-specific survival according to FAS/FASL profile.

    Article Snippet: Anti-FAS monoclonal antibody and anti-FASL monoclonal antibody (Santa Cruz Biotechnology®, USA) were used in the IHC reaction, at a 1∶400 dilution – .

    Techniques: