29928 Search Results


shigella boydii atcc 29928  (ATCC)
92
ATCC shigella boydii atcc 29928
Shigella Boydii Atcc 29928, supplied by ATCC, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/shigella boydii atcc 29928/product/ATCC
Average 92 stars, based on 1 article reviews
shigella boydii atcc 29928 - by Bioz Stars, 2026-02
92/100 stars
  Buy from Supplier
caspase 7  (Santa Cruz Biotechnology)
86
Santa Cruz Biotechnology caspase 7
( a ) p53 protein levels in the liver after a tail vein injection of an associate adenovirus serotype 8 (AAV8) expressing either GFP or Cre in p53floxed mice fed a standard diet (STD) ( n =7 per group). Effects of the liver-specific silencing of p53 on ( b ) in hematoxylin-eosin (upper panel) and oil red O staining (lower panel) of mice liver sections ( n =3 per group); ( c ) total liver TG content, serum AST, ALT and TG levels ( n =8 AAV8-GFP and 10 AAV8-Cre mice); ( d ) liver protein levels of FAS, pJNK/JNK, pIRE/IRE, XBP1s, pPERK, peIF2α/eIF2α, cleaved caspase 3, cleaved caspase 7, ApoB100 and ApoB48; ( e ) mRNA expression of CPT1, ACADM, ACADL and FATP2; ( f ) serum ketone bodies; ( g ) glucose and ( h ) insulin tolerance test ( n =8 AAV8-GFP and 10 AAV8-Cre mice). The values of AAV8 GFP mice were always normalized to 100% ( n =7 per group). Protein GAPDH or transferrin levels were used to normalize protein levels. Dividing lines indicate splicings in the same gel. Uncropped blots of this Figure accompanied by the location of molecular weight markers are shown in . Data are presented as mean±standard error mean (s.e.m.). Statistical significance, * P <0.05 and ** P <0.01, was tested using Student t -test comparing AAV8-GFP and AAV8-Cre mice.
Caspase 7, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/caspase 7/product/Santa Cruz Biotechnology
Average 86 stars, based on 1 article reviews
caspase 7 - by Bioz Stars, 2026-02
86/100 stars
  Buy from Supplier
casp7 shrna  (Santa Cruz Biotechnology)
86
Santa Cruz Biotechnology casp7 shrna
( a ) p53 protein levels in the liver after a tail vein injection of an associate adenovirus serotype 8 (AAV8) expressing either GFP or Cre in p53floxed mice fed a standard diet (STD) ( n =7 per group). Effects of the liver-specific silencing of p53 on ( b ) in hematoxylin-eosin (upper panel) and oil red O staining (lower panel) of mice liver sections ( n =3 per group); ( c ) total liver TG content, serum AST, ALT and TG levels ( n =8 AAV8-GFP and 10 AAV8-Cre mice); ( d ) liver protein levels of FAS, pJNK/JNK, pIRE/IRE, XBP1s, pPERK, peIF2α/eIF2α, cleaved caspase 3, cleaved caspase 7, ApoB100 and ApoB48; ( e ) mRNA expression of CPT1, ACADM, ACADL and FATP2; ( f ) serum ketone bodies; ( g ) glucose and ( h ) insulin tolerance test ( n =8 AAV8-GFP and 10 AAV8-Cre mice). The values of AAV8 GFP mice were always normalized to 100% ( n =7 per group). Protein GAPDH or transferrin levels were used to normalize protein levels. Dividing lines indicate splicings in the same gel. Uncropped blots of this Figure accompanied by the location of molecular weight markers are shown in . Data are presented as mean±standard error mean (s.e.m.). Statistical significance, * P <0.05 and ** P <0.01, was tested using Student t -test comparing AAV8-GFP and AAV8-Cre mice.
Casp7 Shrna, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/casp7 shrna/product/Santa Cruz Biotechnology
Average 86 stars, based on 1 article reviews
casp7 shrna - by Bioz Stars, 2026-02
86/100 stars
  Buy from Supplier

Image Search Results


( a ) p53 protein levels in the liver after a tail vein injection of an associate adenovirus serotype 8 (AAV8) expressing either GFP or Cre in p53floxed mice fed a standard diet (STD) ( n =7 per group). Effects of the liver-specific silencing of p53 on ( b ) in hematoxylin-eosin (upper panel) and oil red O staining (lower panel) of mice liver sections ( n =3 per group); ( c ) total liver TG content, serum AST, ALT and TG levels ( n =8 AAV8-GFP and 10 AAV8-Cre mice); ( d ) liver protein levels of FAS, pJNK/JNK, pIRE/IRE, XBP1s, pPERK, peIF2α/eIF2α, cleaved caspase 3, cleaved caspase 7, ApoB100 and ApoB48; ( e ) mRNA expression of CPT1, ACADM, ACADL and FATP2; ( f ) serum ketone bodies; ( g ) glucose and ( h ) insulin tolerance test ( n =8 AAV8-GFP and 10 AAV8-Cre mice). The values of AAV8 GFP mice were always normalized to 100% ( n =7 per group). Protein GAPDH or transferrin levels were used to normalize protein levels. Dividing lines indicate splicings in the same gel. Uncropped blots of this Figure accompanied by the location of molecular weight markers are shown in . Data are presented as mean±standard error mean (s.e.m.). Statistical significance, * P <0.05 and ** P <0.01, was tested using Student t -test comparing AAV8-GFP and AAV8-Cre mice.

Journal: Nature Communications

Article Title: Hepatic p63 regulates steatosis via IKKβ/ER stress

doi: 10.1038/ncomms15111

Figure Lengend Snippet: ( a ) p53 protein levels in the liver after a tail vein injection of an associate adenovirus serotype 8 (AAV8) expressing either GFP or Cre in p53floxed mice fed a standard diet (STD) ( n =7 per group). Effects of the liver-specific silencing of p53 on ( b ) in hematoxylin-eosin (upper panel) and oil red O staining (lower panel) of mice liver sections ( n =3 per group); ( c ) total liver TG content, serum AST, ALT and TG levels ( n =8 AAV8-GFP and 10 AAV8-Cre mice); ( d ) liver protein levels of FAS, pJNK/JNK, pIRE/IRE, XBP1s, pPERK, peIF2α/eIF2α, cleaved caspase 3, cleaved caspase 7, ApoB100 and ApoB48; ( e ) mRNA expression of CPT1, ACADM, ACADL and FATP2; ( f ) serum ketone bodies; ( g ) glucose and ( h ) insulin tolerance test ( n =8 AAV8-GFP and 10 AAV8-Cre mice). The values of AAV8 GFP mice were always normalized to 100% ( n =7 per group). Protein GAPDH or transferrin levels were used to normalize protein levels. Dividing lines indicate splicings in the same gel. Uncropped blots of this Figure accompanied by the location of molecular weight markers are shown in . Data are presented as mean±standard error mean (s.e.m.). Statistical significance, * P <0.05 and ** P <0.01, was tested using Student t -test comparing AAV8-GFP and AAV8-Cre mice.

Article Snippet: Total protein lysates from liver (20 μg) and THLE2 cells (2 μg) were subjected to SDS-PAGE, electrotransferred onto polyvinylidene difluoride membranes (Millipore) and probed with the indicated antibodies: Fatty Acid Synthase (FAS) (H-300) (sc-20,140), JNK 1/3 (C-17) (sc-474), XBP-1 (M-186) (sc-7,160), p-PERK (TH981) (sc-32,577), p63 (H-129) (sc-11,386), elF2α (FL-315) (sc-11,386), pelF2α (Ser52) (sc-1,01,670), pIKKαβ (ser180/ser181) (sc-23,470-R), p21 (C19) (sc-397) (Santa Cruz Biotechnology, USA); Phospho-SAP/JNK (Thr183/Tyr185) (81E11) Rabbit mAb (#4,668), Caspase 3 (#9,665), Cleaved Caspase 3 (Asp175) (#9,664), Caspase 7 (#9,492), Cleaved Caspase 7 (Asp 198) (#9,491), p53 (1C12) (#2,524), Phospho-p53-Ser15 Antibody (#9,284), Bax Antibody (#2,772) (Cell Signaling, USA); Anti-IKKβ [EPR6,043] (ab124,957), Anti-IKKβ (phosphor Y188) (ab1,94,519), Anti-p73 antibody (EP436Y) (ab40,658), Anti-IRE1 antibody (ab37,073), Anti-SHC (phosphor S36) [6E10] (ab54,518) (Abcam, UK); IRE 1 alpha [p ser 724] (NB100–2,323) (Novus Biologicals, USA); Anti-p63(TA) clone: Poly6,189 (cat:618,902), Anti-p63(ΔN) clone: Poly6,190 (cat:619,002) (Biolegend, USA); GFP (Living Colours , Clontech, Tokio, Japan).

Techniques: Injection, Expressing, Staining, Molecular Weight

( a ) GFP protein levels in the liver and brown adipose tissue (BAT) of WT and p53 null mice after a tail vein injection of adenoviruses encoding either GFP or p53 ( n =5 per group). ( b ) p53 gene expression in the liver of WT and p53 null mice after the injection of adenoviruses encoding either GFP or p53. ( c ) Representative photomicrographs of hematoxylin-eosin (upper panel) and oil red O staining (lower panel) of mice liver sections ( n =3 per group); ( d ) total liver TG content, serum AST and TG levels ( n =6 GFP and 5 p53 in WT mice; n =5 GFP and 4 p53 in KO mice); ( e ) mRNA expression of CPT1, ACADM, ACADL and FATP2; and ( f ) protein levels of FAS, pJNK/JNK, pIRE/IRE, XBP1s, pPERK, peIF2α/eIF2α, cleaved caspase 3, cleaved caspase 7, ApoB100 and ApoB48 in the liver of WT and p53 null mice fed a HFD after the over-expression of hepatic p53. Western blots were performed separately in WT and p53 null mice, and the values of Ad GFP mice were always set to 100% ( n =5 GFP and p53 in both WT and p53 null mice). GAPDH or transferrin were used to normalize protein levels. Dividing lines indicate splicings in the same gel. Uncropped blots of this Figure accompanied by the location of molecular weight markers are shown in . Data are presented as mean±standard error mean (s.e.m.). Statistical significance, * P <0.05 and ** P <0.01, was tested using Student t -test comparing WT and KO mice. ND: non detected.

Journal: Nature Communications

Article Title: Hepatic p63 regulates steatosis via IKKβ/ER stress

doi: 10.1038/ncomms15111

Figure Lengend Snippet: ( a ) GFP protein levels in the liver and brown adipose tissue (BAT) of WT and p53 null mice after a tail vein injection of adenoviruses encoding either GFP or p53 ( n =5 per group). ( b ) p53 gene expression in the liver of WT and p53 null mice after the injection of adenoviruses encoding either GFP or p53. ( c ) Representative photomicrographs of hematoxylin-eosin (upper panel) and oil red O staining (lower panel) of mice liver sections ( n =3 per group); ( d ) total liver TG content, serum AST and TG levels ( n =6 GFP and 5 p53 in WT mice; n =5 GFP and 4 p53 in KO mice); ( e ) mRNA expression of CPT1, ACADM, ACADL and FATP2; and ( f ) protein levels of FAS, pJNK/JNK, pIRE/IRE, XBP1s, pPERK, peIF2α/eIF2α, cleaved caspase 3, cleaved caspase 7, ApoB100 and ApoB48 in the liver of WT and p53 null mice fed a HFD after the over-expression of hepatic p53. Western blots were performed separately in WT and p53 null mice, and the values of Ad GFP mice were always set to 100% ( n =5 GFP and p53 in both WT and p53 null mice). GAPDH or transferrin were used to normalize protein levels. Dividing lines indicate splicings in the same gel. Uncropped blots of this Figure accompanied by the location of molecular weight markers are shown in . Data are presented as mean±standard error mean (s.e.m.). Statistical significance, * P <0.05 and ** P <0.01, was tested using Student t -test comparing WT and KO mice. ND: non detected.

Article Snippet: Total protein lysates from liver (20 μg) and THLE2 cells (2 μg) were subjected to SDS-PAGE, electrotransferred onto polyvinylidene difluoride membranes (Millipore) and probed with the indicated antibodies: Fatty Acid Synthase (FAS) (H-300) (sc-20,140), JNK 1/3 (C-17) (sc-474), XBP-1 (M-186) (sc-7,160), p-PERK (TH981) (sc-32,577), p63 (H-129) (sc-11,386), elF2α (FL-315) (sc-11,386), pelF2α (Ser52) (sc-1,01,670), pIKKαβ (ser180/ser181) (sc-23,470-R), p21 (C19) (sc-397) (Santa Cruz Biotechnology, USA); Phospho-SAP/JNK (Thr183/Tyr185) (81E11) Rabbit mAb (#4,668), Caspase 3 (#9,665), Cleaved Caspase 3 (Asp175) (#9,664), Caspase 7 (#9,492), Cleaved Caspase 7 (Asp 198) (#9,491), p53 (1C12) (#2,524), Phospho-p53-Ser15 Antibody (#9,284), Bax Antibody (#2,772) (Cell Signaling, USA); Anti-IKKβ [EPR6,043] (ab124,957), Anti-IKKβ (phosphor Y188) (ab1,94,519), Anti-p73 antibody (EP436Y) (ab40,658), Anti-IRE1 antibody (ab37,073), Anti-SHC (phosphor S36) [6E10] (ab54,518) (Abcam, UK); IRE 1 alpha [p ser 724] (NB100–2,323) (Novus Biologicals, USA); Anti-p63(TA) clone: Poly6,189 (cat:618,902), Anti-p63(ΔN) clone: Poly6,190 (cat:619,002) (Biolegend, USA); GFP (Living Colours , Clontech, Tokio, Japan).

Techniques: Injection, Expressing, Staining, Over Expression, Western Blot, Molecular Weight

( a ) p63 protein levels in the liver of mice after a tail vein injection of an AAV8 over-expressing either GFP or TAp63α isoform. ( b ) Representative photomicrographs of hematoxylin-eosin (upper panel) and oil red O staining (lower panel) of mice liver sections ( n =4 per group); ( c ) total liver TG content, serum AST, ALT and TG levels ( n =9 AAV8-GFP and 10 AAV8-TAp63α); ( d ) protein levels of FAS, pJNK/JNK, pIRE/IRE, XBP1s, pPERK, peIF2α/eIF2α, cleaved caspase 3, cleaved caspase 7, ApoB100 and ApoB48; and ( e ) mRNA expression of CPT1, ACADM, ACADL and FATP2 in the liver of mice after hepatic over-expression of TAp63 and IP TUDCA administration ( n =7 per group). ( f ) GRP78 protein levels in the liver of mice after a tail vein injection of an Ad over-expressing either GFP or GRP78 ( n =6 per group). ( g ) Representative photomicrographs of hematoxylin-eosin (upper panel) and oil red O staining (lower panel) of mice liver sections ( n =4 per group); ( h ) total liver TG content, serum AST, TG and ketone bodies levels ( n =9 AAV8-GFP and 10 AAV8-TAp63α); ( i ) protein levels of FAS, pIRE/IRE, XBP1s, ApoB100 and ApoB48 ( n =6 per group); and ( j ) mRNA expression of CPT1, ACADM, ACADL and FATP2 in the liver of mice after hepatic over-expression of TAp63α and Ad GRP78 administration ( n =8 per group). Protein GAPDH or transferrin levels were used to normalize protein levels and control values (AAV8 GFP) were normalized to 100%. Dividing lines indicate splicings in the same gel ( n =7 per group). Uncropped blots of this Figure accompanied by the location of molecular weight markers are shown in and . Data are presented as mean±standard error mean (s.e.m.). Statistical significance, * P <0.05, ** P <0.01 and *** P <0.001. For multiple comparison ( c – e , h – j ) a one way ANOVA followed by Bonferroni or Kruskal-Wallis test was performed. Student t -test was used in TAp63alpha and GRP78 liver protein levels ( a , f ).

Journal: Nature Communications

Article Title: Hepatic p63 regulates steatosis via IKKβ/ER stress

doi: 10.1038/ncomms15111

Figure Lengend Snippet: ( a ) p63 protein levels in the liver of mice after a tail vein injection of an AAV8 over-expressing either GFP or TAp63α isoform. ( b ) Representative photomicrographs of hematoxylin-eosin (upper panel) and oil red O staining (lower panel) of mice liver sections ( n =4 per group); ( c ) total liver TG content, serum AST, ALT and TG levels ( n =9 AAV8-GFP and 10 AAV8-TAp63α); ( d ) protein levels of FAS, pJNK/JNK, pIRE/IRE, XBP1s, pPERK, peIF2α/eIF2α, cleaved caspase 3, cleaved caspase 7, ApoB100 and ApoB48; and ( e ) mRNA expression of CPT1, ACADM, ACADL and FATP2 in the liver of mice after hepatic over-expression of TAp63 and IP TUDCA administration ( n =7 per group). ( f ) GRP78 protein levels in the liver of mice after a tail vein injection of an Ad over-expressing either GFP or GRP78 ( n =6 per group). ( g ) Representative photomicrographs of hematoxylin-eosin (upper panel) and oil red O staining (lower panel) of mice liver sections ( n =4 per group); ( h ) total liver TG content, serum AST, TG and ketone bodies levels ( n =9 AAV8-GFP and 10 AAV8-TAp63α); ( i ) protein levels of FAS, pIRE/IRE, XBP1s, ApoB100 and ApoB48 ( n =6 per group); and ( j ) mRNA expression of CPT1, ACADM, ACADL and FATP2 in the liver of mice after hepatic over-expression of TAp63α and Ad GRP78 administration ( n =8 per group). Protein GAPDH or transferrin levels were used to normalize protein levels and control values (AAV8 GFP) were normalized to 100%. Dividing lines indicate splicings in the same gel ( n =7 per group). Uncropped blots of this Figure accompanied by the location of molecular weight markers are shown in and . Data are presented as mean±standard error mean (s.e.m.). Statistical significance, * P <0.05, ** P <0.01 and *** P <0.001. For multiple comparison ( c – e , h – j ) a one way ANOVA followed by Bonferroni or Kruskal-Wallis test was performed. Student t -test was used in TAp63alpha and GRP78 liver protein levels ( a , f ).

Article Snippet: Total protein lysates from liver (20 μg) and THLE2 cells (2 μg) were subjected to SDS-PAGE, electrotransferred onto polyvinylidene difluoride membranes (Millipore) and probed with the indicated antibodies: Fatty Acid Synthase (FAS) (H-300) (sc-20,140), JNK 1/3 (C-17) (sc-474), XBP-1 (M-186) (sc-7,160), p-PERK (TH981) (sc-32,577), p63 (H-129) (sc-11,386), elF2α (FL-315) (sc-11,386), pelF2α (Ser52) (sc-1,01,670), pIKKαβ (ser180/ser181) (sc-23,470-R), p21 (C19) (sc-397) (Santa Cruz Biotechnology, USA); Phospho-SAP/JNK (Thr183/Tyr185) (81E11) Rabbit mAb (#4,668), Caspase 3 (#9,665), Cleaved Caspase 3 (Asp175) (#9,664), Caspase 7 (#9,492), Cleaved Caspase 7 (Asp 198) (#9,491), p53 (1C12) (#2,524), Phospho-p53-Ser15 Antibody (#9,284), Bax Antibody (#2,772) (Cell Signaling, USA); Anti-IKKβ [EPR6,043] (ab124,957), Anti-IKKβ (phosphor Y188) (ab1,94,519), Anti-p73 antibody (EP436Y) (ab40,658), Anti-IRE1 antibody (ab37,073), Anti-SHC (phosphor S36) [6E10] (ab54,518) (Abcam, UK); IRE 1 alpha [p ser 724] (NB100–2,323) (Novus Biologicals, USA); Anti-p63(TA) clone: Poly6,189 (cat:618,902), Anti-p63(ΔN) clone: Poly6,190 (cat:619,002) (Biolegend, USA); GFP (Living Colours , Clontech, Tokio, Japan).

Techniques: Injection, Expressing, Staining, Over Expression, Molecular Weight