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96
Proteintech scd1
(A): (left) Representative immunohistochemical staining of the skin using an anti -ABCB1 antibody. (center) Comparison of PPARg and <t>SCD1</t> gene expression. (right) Representative immunohistochemical staining of the skin using an anti -SCD1 antibody. ∗∗ no significant difference; ∗P < 0.05. (B): Representative immunohistochemical staining of the skin using an anti -ki67 antibody and Nuclear Ki67 IHC score. Expression of ki67 was significantly reduced in Tg compared to wild type. ∗P < 0.05. (C): Representative immunohistochemical staining of the skin using an anti -Loricrin antibody. (D): Representative immunohistochemical staining of the skin using an anti-YAP antibody.
Scd1, supplied by Proteintech, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/scd1/product/Proteintech
Average 96 stars, based on 1 article reviews
scd1 - by Bioz Stars, 2026-03
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96
Proteintech anti scd1
(A): (left) Representative immunohistochemical staining of the skin using an anti -ABCB1 antibody. (center) Comparison of PPARg and <t>SCD1</t> gene expression. (right) Representative immunohistochemical staining of the skin using an anti -SCD1 antibody. ∗∗ no significant difference; ∗P < 0.05. (B): Representative immunohistochemical staining of the skin using an anti -ki67 antibody and Nuclear Ki67 IHC score. Expression of ki67 was significantly reduced in Tg compared to wild type. ∗P < 0.05. (C): Representative immunohistochemical staining of the skin using an anti -Loricrin antibody. (D): Representative immunohistochemical staining of the skin using an anti-YAP antibody.
Anti Scd1, supplied by Proteintech, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/anti scd1/product/Proteintech
Average 96 stars, based on 1 article reviews
anti scd1 - by Bioz Stars, 2026-03
96/100 stars
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96
Proteintech scd
(A): (left) Representative immunohistochemical staining of the skin using an anti -ABCB1 antibody. (center) Comparison of PPARg and <t>SCD1</t> gene expression. (right) Representative immunohistochemical staining of the skin using an anti -SCD1 antibody. ∗∗ no significant difference; ∗P < 0.05. (B): Representative immunohistochemical staining of the skin using an anti -ki67 antibody and Nuclear Ki67 IHC score. Expression of ki67 was significantly reduced in Tg compared to wild type. ∗P < 0.05. (C): Representative immunohistochemical staining of the skin using an anti -Loricrin antibody. (D): Representative immunohistochemical staining of the skin using an anti-YAP antibody.
Scd, supplied by Proteintech, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/scd/product/Proteintech
Average 96 stars, based on 1 article reviews
scd - by Bioz Stars, 2026-03
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96
Proteintech desaturase 1
(A): (left) Representative immunohistochemical staining of the skin using an anti -ABCB1 antibody. (center) Comparison of PPARg and <t>SCD1</t> gene expression. (right) Representative immunohistochemical staining of the skin using an anti -SCD1 antibody. ∗∗ no significant difference; ∗P < 0.05. (B): Representative immunohistochemical staining of the skin using an anti -ki67 antibody and Nuclear Ki67 IHC score. Expression of ki67 was significantly reduced in Tg compared to wild type. ∗P < 0.05. (C): Representative immunohistochemical staining of the skin using an anti -Loricrin antibody. (D): Representative immunohistochemical staining of the skin using an anti-YAP antibody.
Desaturase 1, supplied by Proteintech, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/desaturase 1/product/Proteintech
Average 96 stars, based on 1 article reviews
desaturase 1 - by Bioz Stars, 2026-03
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96
Proteintech stearoyl coenzyme
(A): (left) Representative immunohistochemical staining of the skin using an anti -ABCB1 antibody. (center) Comparison of PPARg and <t>SCD1</t> gene expression. (right) Representative immunohistochemical staining of the skin using an anti -SCD1 antibody. ∗∗ no significant difference; ∗P < 0.05. (B): Representative immunohistochemical staining of the skin using an anti -ki67 antibody and Nuclear Ki67 IHC score. Expression of ki67 was significantly reduced in Tg compared to wild type. ∗P < 0.05. (C): Representative immunohistochemical staining of the skin using an anti -Loricrin antibody. (D): Representative immunohistochemical staining of the skin using an anti-YAP antibody.
Stearoyl Coenzyme, supplied by Proteintech, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/stearoyl coenzyme/product/Proteintech
Average 96 stars, based on 1 article reviews
stearoyl coenzyme - by Bioz Stars, 2026-03
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96
Proteintech fatty acid desaturase 2 fads2
R. hominis intervention promoted LA metabolism in mice, and its effect on reversing the NR in mice depended on PLA2 (A) The PCA score plot in negative and positive ion modes. In the negative ion mode, the prediction rate (Q2) of the PCA-X model is 0.599, and the interpretation rate (R2X) is 0.771. The prediction rate (Q2) of the PCA-X model in positive ion mode is 0.487, and the interpretation rate (R2X) is 0.712. (B) Enrichment analysis of differential metabolites. (C–E) The serum abundance of (C) PC (18:3/16:0), (D) LA, and (E) SDA. (F) Schematic diagram of LA metabolism. The blue background represents metabolites, while the green background represents enzymes. The red font represents the substances detected in the study. (G) Western blot analysis of PLA2G and <t>FADS2</t> proteins in the livers of mice after R. hominis administration. (H) The activity of PLA2 after darapladib intervention. (I) Oral glucose tolerance test (OGTT) curve and its area under the curve (AUC). (J) Insulin tolerance test (ITT) curve and its AUC. (K) Homeostatic model assessment for insulin resistance (HOMA-IR) after drug administration. Data are expressed as the mean ± SD ( n = 7–8); ∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗ p < 0.001, ∗∗∗∗ p < 0.0001, as determined by one-way ANOVA with Holm-Sidak’s post hoc test. ANOVA, analysis of variance; PC, phosphatidylcholine; NR, non-response; NCD, normal chow diet; R.h, Roseburia hominis ; PLA2, phospholipase A2; FADS2, fatty acid desaturase 2; GAPDH, glyceraldehyde-3-phosphate dehydrogenase; PCA, principal-component analysis.
Fatty Acid Desaturase 2 Fads2, supplied by Proteintech, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/fatty acid desaturase 2 fads2/product/Proteintech
Average 96 stars, based on 1 article reviews
fatty acid desaturase 2 fads2 - by Bioz Stars, 2026-03
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96
Proteintech anti scd1 primary antibody
R. hominis intervention promoted LA metabolism in mice, and its effect on reversing the NR in mice depended on PLA2 (A) The PCA score plot in negative and positive ion modes. In the negative ion mode, the prediction rate (Q2) of the PCA-X model is 0.599, and the interpretation rate (R2X) is 0.771. The prediction rate (Q2) of the PCA-X model in positive ion mode is 0.487, and the interpretation rate (R2X) is 0.712. (B) Enrichment analysis of differential metabolites. (C–E) The serum abundance of (C) PC (18:3/16:0), (D) LA, and (E) SDA. (F) Schematic diagram of LA metabolism. The blue background represents metabolites, while the green background represents enzymes. The red font represents the substances detected in the study. (G) Western blot analysis of PLA2G and <t>FADS2</t> proteins in the livers of mice after R. hominis administration. (H) The activity of PLA2 after darapladib intervention. (I) Oral glucose tolerance test (OGTT) curve and its area under the curve (AUC). (J) Insulin tolerance test (ITT) curve and its AUC. (K) Homeostatic model assessment for insulin resistance (HOMA-IR) after drug administration. Data are expressed as the mean ± SD ( n = 7–8); ∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗ p < 0.001, ∗∗∗∗ p < 0.0001, as determined by one-way ANOVA with Holm-Sidak’s post hoc test. ANOVA, analysis of variance; PC, phosphatidylcholine; NR, non-response; NCD, normal chow diet; R.h, Roseburia hominis ; PLA2, phospholipase A2; FADS2, fatty acid desaturase 2; GAPDH, glyceraldehyde-3-phosphate dehydrogenase; PCA, principal-component analysis.
Anti Scd1 Primary Antibody, supplied by Proteintech, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/anti scd1 primary antibody/product/Proteintech
Average 96 stars, based on 1 article reviews
anti scd1 primary antibody - by Bioz Stars, 2026-03
96/100 stars
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(A): (left) Representative immunohistochemical staining of the skin using an anti -ABCB1 antibody. (center) Comparison of PPARg and SCD1 gene expression. (right) Representative immunohistochemical staining of the skin using an anti -SCD1 antibody. ∗∗ no significant difference; ∗P < 0.05. (B): Representative immunohistochemical staining of the skin using an anti -ki67 antibody and Nuclear Ki67 IHC score. Expression of ki67 was significantly reduced in Tg compared to wild type. ∗P < 0.05. (C): Representative immunohistochemical staining of the skin using an anti -Loricrin antibody. (D): Representative immunohistochemical staining of the skin using an anti-YAP antibody.

Journal: Biochemistry and Biophysics Reports

Article Title: TMEM207-mediated the impairment of skin regeneration through YAP sequestration in an allergic contact dermatitis model

doi: 10.1016/j.bbrep.2025.102409

Figure Lengend Snippet: (A): (left) Representative immunohistochemical staining of the skin using an anti -ABCB1 antibody. (center) Comparison of PPARg and SCD1 gene expression. (right) Representative immunohistochemical staining of the skin using an anti -SCD1 antibody. ∗∗ no significant difference; ∗P < 0.05. (B): Representative immunohistochemical staining of the skin using an anti -ki67 antibody and Nuclear Ki67 IHC score. Expression of ki67 was significantly reduced in Tg compared to wild type. ∗P < 0.05. (C): Representative immunohistochemical staining of the skin using an anti -Loricrin antibody. (D): Representative immunohistochemical staining of the skin using an anti-YAP antibody.

Article Snippet: Rabbit anti -GAPDH antibodies were obtained from Sigma-Aldrich (St. Louis, MO, USA), and rabbit anti -ABCB1, anti -SCD1, anti -NEDD4, anti -Ki67, anti -Loricrin, and anti-YAP antibodies were purchased from ProteinTech (Proteintech, Inc., USA).

Techniques: Immunohistochemical staining, Staining, Comparison, Gene Expression, Expressing

R. hominis intervention promoted LA metabolism in mice, and its effect on reversing the NR in mice depended on PLA2 (A) The PCA score plot in negative and positive ion modes. In the negative ion mode, the prediction rate (Q2) of the PCA-X model is 0.599, and the interpretation rate (R2X) is 0.771. The prediction rate (Q2) of the PCA-X model in positive ion mode is 0.487, and the interpretation rate (R2X) is 0.712. (B) Enrichment analysis of differential metabolites. (C–E) The serum abundance of (C) PC (18:3/16:0), (D) LA, and (E) SDA. (F) Schematic diagram of LA metabolism. The blue background represents metabolites, while the green background represents enzymes. The red font represents the substances detected in the study. (G) Western blot analysis of PLA2G and FADS2 proteins in the livers of mice after R. hominis administration. (H) The activity of PLA2 after darapladib intervention. (I) Oral glucose tolerance test (OGTT) curve and its area under the curve (AUC). (J) Insulin tolerance test (ITT) curve and its AUC. (K) Homeostatic model assessment for insulin resistance (HOMA-IR) after drug administration. Data are expressed as the mean ± SD ( n = 7–8); ∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗ p < 0.001, ∗∗∗∗ p < 0.0001, as determined by one-way ANOVA with Holm-Sidak’s post hoc test. ANOVA, analysis of variance; PC, phosphatidylcholine; NR, non-response; NCD, normal chow diet; R.h, Roseburia hominis ; PLA2, phospholipase A2; FADS2, fatty acid desaturase 2; GAPDH, glyceraldehyde-3-phosphate dehydrogenase; PCA, principal-component analysis.

Journal: iScience

Article Title: Roseburia hominis enriched by baicalin reverses the non-response to metformin via upregulating linolenic acid metabolism

doi: 10.1016/j.isci.2025.113892

Figure Lengend Snippet: R. hominis intervention promoted LA metabolism in mice, and its effect on reversing the NR in mice depended on PLA2 (A) The PCA score plot in negative and positive ion modes. In the negative ion mode, the prediction rate (Q2) of the PCA-X model is 0.599, and the interpretation rate (R2X) is 0.771. The prediction rate (Q2) of the PCA-X model in positive ion mode is 0.487, and the interpretation rate (R2X) is 0.712. (B) Enrichment analysis of differential metabolites. (C–E) The serum abundance of (C) PC (18:3/16:0), (D) LA, and (E) SDA. (F) Schematic diagram of LA metabolism. The blue background represents metabolites, while the green background represents enzymes. The red font represents the substances detected in the study. (G) Western blot analysis of PLA2G and FADS2 proteins in the livers of mice after R. hominis administration. (H) The activity of PLA2 after darapladib intervention. (I) Oral glucose tolerance test (OGTT) curve and its area under the curve (AUC). (J) Insulin tolerance test (ITT) curve and its AUC. (K) Homeostatic model assessment for insulin resistance (HOMA-IR) after drug administration. Data are expressed as the mean ± SD ( n = 7–8); ∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗ p < 0.001, ∗∗∗∗ p < 0.0001, as determined by one-way ANOVA with Holm-Sidak’s post hoc test. ANOVA, analysis of variance; PC, phosphatidylcholine; NR, non-response; NCD, normal chow diet; R.h, Roseburia hominis ; PLA2, phospholipase A2; FADS2, fatty acid desaturase 2; GAPDH, glyceraldehyde-3-phosphate dehydrogenase; PCA, principal-component analysis.

Article Snippet: These membranes were then incubated at 4°C overnight with primary antibodies against AMP-activated protein kinase (AMPK) (Proteintech, Cat# 10929-2-AP, RRID: AB_2169568 , 1:4,000), insulin receptor substrate 1 (IRS1) (Proteintech, Cat# 17509-1-AP, RRID: AB_10596914 , 1:1,000), phospho-AMPKα (Thr172) (40H9) (Cell Signaling Technology, Cat# 2535, RRID: AB_331250 , 1:1,000), phospho-IRS-1 (Ser636/639) (Cell Signaling Technology, Cat# 2388, RRID: AB_330339 , 1:1,000), phosphoenolpyruvate carboxykinase (PCK) (Proteintech, Cat# 16754-1-AP, RRID: AB_2160031 , 1:30,000), glucose-6-phosphatase (G6PC) (Proteintech, Cat# 66860-1-Ig, RRID: AB_2882199 , 1:5,000), mammalian target of rapamycin (mTOR) (Proteintech, Cat# 66888-1-Ig, RRID: AB_2882219 , 1:30,000), fatty acid desaturase 2 (FADS2) (Proteintech, Cat# 28034-1-AP, RRID: AB_2918142 , 1:4,000), phospholipase A2 group (PLA2G) (Proteintech, Cat# 18088-1-AP, RRID: AB_10859777 , 1:1,000), acetyl-CoA Carboxylase 1 (ACC1) (Proteintech, Cat# 21923-1-AP, RRID: AB_11042445 , 1:4,000), carnitine palmitoyl transferase 1 (CPT1) (Proteintech, Cat# 15184-1-AP, RRID: AB_2084676 , 1:50,000), glyceraldehyde-3-phosphate dehydrogenase (GAPDH) (Proteintech, Cat# 10494-1-AP, RRID: AB_2263076 , 1:20,000), β-tubulin (Proteintech, Cat# 10094-1-AP, RRID: AB_2210695 , 1:10,000).

Techniques: Western Blot, Activity Assay