fb cf growth differentiation factor 11 Search Results


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Shanghai Korain Biotech Co Ltd gdf 11
Gdf 11, supplied by Shanghai Korain Biotech Co Ltd, 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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Guangzhou JET Bio-Filtration human gdf11 (growth differentiation factor 11) elisa kit
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Cusabio mouse gdf11 elisa kits
(A–F) Protein expression in GAS muscle. (A) Representative immunoblots of soluble active myostatin (MSTN) C-terminal dimer and eukaryotic elongation factor 2 (EF2) expression in muscle from sets of 4 mice, castrated for the indicated times or sham castrated. Lanes of immunoblots marked “C” contain identical control sample for interblot comparison. (B) Quantification of relative MSTN levels for castrated mice (red) or sham-castrated mice (blue), from 3 determinations for each muscle (see Supplemental Figure 5 for additional immunoblots and supplemental materials for full, uncut gels). ELISA-determined protein levels of soluble active activin AA dimer (C), activin BB dimer (D), activin AB dimer (E), and soluble <t>GDF11</t> (F), in muscle from 4 mice at each time point, measured 3 times each. (G–L) Protein expression in TRI muscle. (G) Representative immunoblot of MSTN and EF2 expression, as in A. (H) Quantification of MSTN levels, as in B. ELISA-determined protein levels of soluble active activin AA dimer (I), activin BB dimer (J), activin AB dimer (K), and soluble GDF11 (L), from 4 mice at each time point, measured 3 times each. Columns are sham-castrated normalized means at each time; bars are SEM. Individual mouse levels are indicated by open circles. *P < 0.05, **P < 0.01, and ***P < 0.001 versus sham-castrated group determined using 1-way ANOVA and Bonferroni’s correction (B and H) or Dunnett’s test (C–F and I–L).
Mouse Gdf11 Elisa Kits, supplied by Cusabio, used in various techniques. Bioz Stars score: 91/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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(A–F) Protein expression in GAS muscle. (A) Representative immunoblots of soluble active myostatin (MSTN) C-terminal dimer and eukaryotic elongation factor 2 (EF2) expression in muscle from sets of 4 mice, castrated for the indicated times or sham castrated. Lanes of immunoblots marked “C” contain identical control sample for interblot comparison. (B) Quantification of relative MSTN levels for castrated mice (red) or sham-castrated mice (blue), from 3 determinations for each muscle (see Supplemental Figure 5 for additional immunoblots and supplemental materials for full, uncut gels). ELISA-determined protein levels of soluble active activin AA dimer (C), activin BB dimer (D), activin AB dimer (E), and soluble <t>GDF11</t> (F), in muscle from 4 mice at each time point, measured 3 times each. (G–L) Protein expression in TRI muscle. (G) Representative immunoblot of MSTN and EF2 expression, as in A. (H) Quantification of MSTN levels, as in B. ELISA-determined protein levels of soluble active activin AA dimer (I), activin BB dimer (J), activin AB dimer (K), and soluble GDF11 (L), from 4 mice at each time point, measured 3 times each. Columns are sham-castrated normalized means at each time; bars are SEM. Individual mouse levels are indicated by open circles. *P < 0.05, **P < 0.01, and ***P < 0.001 versus sham-castrated group determined using 1-way ANOVA and Bonferroni’s correction (B and H) or Dunnett’s test (C–F and I–L).
Csb Ep009344hu, supplied by Cusabio, used in various techniques. Bioz Stars score: 91/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Cusabio cardiac troponin i ctn i
(A–F) Protein expression in GAS muscle. (A) Representative immunoblots of soluble active myostatin (MSTN) C-terminal dimer and eukaryotic elongation factor 2 (EF2) expression in muscle from sets of 4 mice, castrated for the indicated times or sham castrated. Lanes of immunoblots marked “C” contain identical control sample for interblot comparison. (B) Quantification of relative MSTN levels for castrated mice (red) or sham-castrated mice (blue), from 3 determinations for each muscle (see Supplemental Figure 5 for additional immunoblots and supplemental materials for full, uncut gels). ELISA-determined protein levels of soluble active activin AA dimer (C), activin BB dimer (D), activin AB dimer (E), and soluble <t>GDF11</t> (F), in muscle from 4 mice at each time point, measured 3 times each. (G–L) Protein expression in TRI muscle. (G) Representative immunoblot of MSTN and EF2 expression, as in A. (H) Quantification of MSTN levels, as in B. ELISA-determined protein levels of soluble active activin AA dimer (I), activin BB dimer (J), activin AB dimer (K), and soluble GDF11 (L), from 4 mice at each time point, measured 3 times each. Columns are sham-castrated normalized means at each time; bars are SEM. Individual mouse levels are indicated by open circles. *P < 0.05, **P < 0.01, and ***P < 0.001 versus sham-castrated group determined using 1-way ANOVA and Bonferroni’s correction (B and H) or Dunnett’s test (C–F and I–L).
Cardiac Troponin I Ctn I, supplied by Cusabio, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Neurescence inc growth differentiation factor 11
(A–F) Protein expression in GAS muscle. (A) Representative immunoblots of soluble active myostatin (MSTN) C-terminal dimer and eukaryotic elongation factor 2 (EF2) expression in muscle from sets of 4 mice, castrated for the indicated times or sham castrated. Lanes of immunoblots marked “C” contain identical control sample for interblot comparison. (B) Quantification of relative MSTN levels for castrated mice (red) or sham-castrated mice (blue), from 3 determinations for each muscle (see Supplemental Figure 5 for additional immunoblots and supplemental materials for full, uncut gels). ELISA-determined protein levels of soluble active activin AA dimer (C), activin BB dimer (D), activin AB dimer (E), and soluble <t>GDF11</t> (F), in muscle from 4 mice at each time point, measured 3 times each. (G–L) Protein expression in TRI muscle. (G) Representative immunoblot of MSTN and EF2 expression, as in A. (H) Quantification of MSTN levels, as in B. ELISA-determined protein levels of soluble active activin AA dimer (I), activin BB dimer (J), activin AB dimer (K), and soluble GDF11 (L), from 4 mice at each time point, measured 3 times each. Columns are sham-castrated normalized means at each time; bars are SEM. Individual mouse levels are indicated by open circles. *P < 0.05, **P < 0.01, and ***P < 0.001 versus sham-castrated group determined using 1-way ANOVA and Bonferroni’s correction (B and H) or Dunnett’s test (C–F and I–L).
Growth Differentiation Factor 11, supplied by Neurescence inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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PeproTech growth/differentiation factor-11, bmp-11
(A–F) Protein expression in GAS muscle. (A) Representative immunoblots of soluble active myostatin (MSTN) C-terminal dimer and eukaryotic elongation factor 2 (EF2) expression in muscle from sets of 4 mice, castrated for the indicated times or sham castrated. Lanes of immunoblots marked “C” contain identical control sample for interblot comparison. (B) Quantification of relative MSTN levels for castrated mice (red) or sham-castrated mice (blue), from 3 determinations for each muscle (see Supplemental Figure 5 for additional immunoblots and supplemental materials for full, uncut gels). ELISA-determined protein levels of soluble active activin AA dimer (C), activin BB dimer (D), activin AB dimer (E), and soluble <t>GDF11</t> (F), in muscle from 4 mice at each time point, measured 3 times each. (G–L) Protein expression in TRI muscle. (G) Representative immunoblot of MSTN and EF2 expression, as in A. (H) Quantification of MSTN levels, as in B. ELISA-determined protein levels of soluble active activin AA dimer (I), activin BB dimer (J), activin AB dimer (K), and soluble GDF11 (L), from 4 mice at each time point, measured 3 times each. Columns are sham-castrated normalized means at each time; bars are SEM. Individual mouse levels are indicated by open circles. *P < 0.05, **P < 0.01, and ***P < 0.001 versus sham-castrated group determined using 1-way ANOVA and Bonferroni’s correction (B and H) or Dunnett’s test (C–F and I–L).
Growth/Differentiation Factor 11, Bmp 11, supplied by PeproTech, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Novatein Inc human growth differentiation factor 11 gdf11 elisa kit
(A–F) Protein expression in GAS muscle. (A) Representative immunoblots of soluble active myostatin (MSTN) C-terminal dimer and eukaryotic elongation factor 2 (EF2) expression in muscle from sets of 4 mice, castrated for the indicated times or sham castrated. Lanes of immunoblots marked “C” contain identical control sample for interblot comparison. (B) Quantification of relative MSTN levels for castrated mice (red) or sham-castrated mice (blue), from 3 determinations for each muscle (see Supplemental Figure 5 for additional immunoblots and supplemental materials for full, uncut gels). ELISA-determined protein levels of soluble active activin AA dimer (C), activin BB dimer (D), activin AB dimer (E), and soluble <t>GDF11</t> (F), in muscle from 4 mice at each time point, measured 3 times each. (G–L) Protein expression in TRI muscle. (G) Representative immunoblot of MSTN and EF2 expression, as in A. (H) Quantification of MSTN levels, as in B. ELISA-determined protein levels of soluble active activin AA dimer (I), activin BB dimer (J), activin AB dimer (K), and soluble GDF11 (L), from 4 mice at each time point, measured 3 times each. Columns are sham-castrated normalized means at each time; bars are SEM. Individual mouse levels are indicated by open circles. *P < 0.05, **P < 0.01, and ***P < 0.001 versus sham-castrated group determined using 1-way ANOVA and Bonferroni’s correction (B and H) or Dunnett’s test (C–F and I–L).
Human Growth Differentiation Factor 11 Gdf11 Elisa Kit, supplied by Novatein Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Boster Bio anti jund
(A–F) Protein expression in GAS muscle. (A) Representative immunoblots of soluble active myostatin (MSTN) C-terminal dimer and eukaryotic elongation factor 2 (EF2) expression in muscle from sets of 4 mice, castrated for the indicated times or sham castrated. Lanes of immunoblots marked “C” contain identical control sample for interblot comparison. (B) Quantification of relative MSTN levels for castrated mice (red) or sham-castrated mice (blue), from 3 determinations for each muscle (see Supplemental Figure 5 for additional immunoblots and supplemental materials for full, uncut gels). ELISA-determined protein levels of soluble active activin AA dimer (C), activin BB dimer (D), activin AB dimer (E), and soluble <t>GDF11</t> (F), in muscle from 4 mice at each time point, measured 3 times each. (G–L) Protein expression in TRI muscle. (G) Representative immunoblot of MSTN and EF2 expression, as in A. (H) Quantification of MSTN levels, as in B. ELISA-determined protein levels of soluble active activin AA dimer (I), activin BB dimer (J), activin AB dimer (K), and soluble GDF11 (L), from 4 mice at each time point, measured 3 times each. Columns are sham-castrated normalized means at each time; bars are SEM. Individual mouse levels are indicated by open circles. *P < 0.05, **P < 0.01, and ***P < 0.001 versus sham-castrated group determined using 1-way ANOVA and Bonferroni’s correction (B and H) or Dunnett’s test (C–F and I–L).
Anti Jund, supplied by Boster Bio, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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(A–F) Protein expression in GAS muscle. (A) Representative immunoblots of soluble active myostatin (MSTN) C-terminal dimer and eukaryotic elongation factor 2 (EF2) expression in muscle from sets of 4 mice, castrated for the indicated times or sham castrated. Lanes of immunoblots marked “C” contain identical control sample for interblot comparison. (B) Quantification of relative MSTN levels for castrated mice (red) or sham-castrated mice (blue), from 3 determinations for each muscle (see Supplemental Figure 5 for additional immunoblots and supplemental materials for full, uncut gels). ELISA-determined protein levels of soluble active activin AA dimer (C), activin BB dimer (D), activin AB dimer (E), and soluble <t>GDF11</t> (F), in muscle from 4 mice at each time point, measured 3 times each. (G–L) Protein expression in TRI muscle. (G) Representative immunoblot of MSTN and EF2 expression, as in A. (H) Quantification of MSTN levels, as in B. ELISA-determined protein levels of soluble active activin AA dimer (I), activin BB dimer (J), activin AB dimer (K), and soluble GDF11 (L), from 4 mice at each time point, measured 3 times each. Columns are sham-castrated normalized means at each time; bars are SEM. Individual mouse levels are indicated by open circles. *P < 0.05, **P < 0.01, and ***P < 0.001 versus sham-castrated group determined using 1-way ANOVA and Bonferroni’s correction (B and H) or Dunnett’s test (C–F and I–L).
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Image Search Results


(A–F) Protein expression in GAS muscle. (A) Representative immunoblots of soluble active myostatin (MSTN) C-terminal dimer and eukaryotic elongation factor 2 (EF2) expression in muscle from sets of 4 mice, castrated for the indicated times or sham castrated. Lanes of immunoblots marked “C” contain identical control sample for interblot comparison. (B) Quantification of relative MSTN levels for castrated mice (red) or sham-castrated mice (blue), from 3 determinations for each muscle (see Supplemental Figure 5 for additional immunoblots and supplemental materials for full, uncut gels). ELISA-determined protein levels of soluble active activin AA dimer (C), activin BB dimer (D), activin AB dimer (E), and soluble GDF11 (F), in muscle from 4 mice at each time point, measured 3 times each. (G–L) Protein expression in TRI muscle. (G) Representative immunoblot of MSTN and EF2 expression, as in A. (H) Quantification of MSTN levels, as in B. ELISA-determined protein levels of soluble active activin AA dimer (I), activin BB dimer (J), activin AB dimer (K), and soluble GDF11 (L), from 4 mice at each time point, measured 3 times each. Columns are sham-castrated normalized means at each time; bars are SEM. Individual mouse levels are indicated by open circles. *P < 0.05, **P < 0.01, and ***P < 0.001 versus sham-castrated group determined using 1-way ANOVA and Bonferroni’s correction (B and H) or Dunnett’s test (C–F and I–L).

Journal: JCI Insight

Article Title: Prostate tumor–derived GDF11 accelerates androgen deprivation therapy–induced sarcopenia

doi: 10.1172/jci.insight.127018

Figure Lengend Snippet: (A–F) Protein expression in GAS muscle. (A) Representative immunoblots of soluble active myostatin (MSTN) C-terminal dimer and eukaryotic elongation factor 2 (EF2) expression in muscle from sets of 4 mice, castrated for the indicated times or sham castrated. Lanes of immunoblots marked “C” contain identical control sample for interblot comparison. (B) Quantification of relative MSTN levels for castrated mice (red) or sham-castrated mice (blue), from 3 determinations for each muscle (see Supplemental Figure 5 for additional immunoblots and supplemental materials for full, uncut gels). ELISA-determined protein levels of soluble active activin AA dimer (C), activin BB dimer (D), activin AB dimer (E), and soluble GDF11 (F), in muscle from 4 mice at each time point, measured 3 times each. (G–L) Protein expression in TRI muscle. (G) Representative immunoblot of MSTN and EF2 expression, as in A. (H) Quantification of MSTN levels, as in B. ELISA-determined protein levels of soluble active activin AA dimer (I), activin BB dimer (J), activin AB dimer (K), and soluble GDF11 (L), from 4 mice at each time point, measured 3 times each. Columns are sham-castrated normalized means at each time; bars are SEM. Individual mouse levels are indicated by open circles. *P < 0.05, **P < 0.01, and ***P < 0.001 versus sham-castrated group determined using 1-way ANOVA and Bonferroni’s correction (B and H) or Dunnett’s test (C–F and I–L).

Article Snippet: ELISA kits used were human/mouse/rat activin A ELISA kit (Quantikine DAC00B, R&D Systems, Bio-Techne), mouse activin B ELISA kit (E15932m, Cusabio Biotech Co., Ltd.), mouse activin AB and mouse GDF11 ELISA kits (CEA158Mu and SEC113Mu, respectively, Cloud-Clone Corp.), and total myostatin ELISA kit (Quantikine DGDF80, R&D Systems, Bio-Techne).

Techniques: Expressing, Western Blot, Control, Comparison, Enzyme-linked Immunosorbent Assay

(A) Grip strength after castration or sham-castration of mice treated with PBS, ActRIIB-Fc, or anti-GDF11 antibody. (B) Dissected skeletal muscle mass 10 weeks after castration by dissection and weighing. (C) Lean body mass by quantitative NMR (qNMR), as percentage of sham-castrated mice. Mean indicated as lines or columns, SEM as bars; n = 3–5/group, indicated by open circles. *P < 0.05 and **P < 0.01 for ActRIIB-Fc treated castrated versus vehicle-treated castrated mice determined using 2-way ANOVA and Tukey’s honestly significant differences (HSD) test. See Supplemental Figure 7 for additional information.

Journal: JCI Insight

Article Title: Prostate tumor–derived GDF11 accelerates androgen deprivation therapy–induced sarcopenia

doi: 10.1172/jci.insight.127018

Figure Lengend Snippet: (A) Grip strength after castration or sham-castration of mice treated with PBS, ActRIIB-Fc, or anti-GDF11 antibody. (B) Dissected skeletal muscle mass 10 weeks after castration by dissection and weighing. (C) Lean body mass by quantitative NMR (qNMR), as percentage of sham-castrated mice. Mean indicated as lines or columns, SEM as bars; n = 3–5/group, indicated by open circles. *P < 0.05 and **P < 0.01 for ActRIIB-Fc treated castrated versus vehicle-treated castrated mice determined using 2-way ANOVA and Tukey’s honestly significant differences (HSD) test. See Supplemental Figure 7 for additional information.

Article Snippet: ELISA kits used were human/mouse/rat activin A ELISA kit (Quantikine DAC00B, R&D Systems, Bio-Techne), mouse activin B ELISA kit (E15932m, Cusabio Biotech Co., Ltd.), mouse activin AB and mouse GDF11 ELISA kits (CEA158Mu and SEC113Mu, respectively, Cloud-Clone Corp.), and total myostatin ELISA kit (Quantikine DGDF80, R&D Systems, Bio-Techne).

Techniques: Dissection

(A–C) GDF11 and myostatin protein expression in tumor. (A) ELISA-determined levels of GDF11 in prostate tumor tissue, from 4 mice at each time, measured 3 times. (B) Representative immunoblots of soluble active myostatin C-terminal dimer (MSTN) and eukaryotic elongation factor 2 (EF2) expression in prostate tumor tissue from sets of 4 mice, castrated for the indicated times or sham castrated. Lanes of immunoblots marked “C” contain identical control sample for interblot comparison. (C) Quantification of MSTN levels in tumor tissue from castrated (red) or sham-castrated (blue) mice, from 3 determinations for each tumor (see Supplemental Figure 5 for additional immunoblots and supplemental materials for full, uncut gels). (D–F) GDF11 and myostatin protein expression in serum. (D) ELISA-determined levels of GDF11 in serum, from 4 mice at each time, measured 3 times. (E) Representative immunoblots of MSTN expression in equal quantities of serum protein from the 4 mice in A. (F) Quantification of MSTN levels in serum, as in B. (G–I) Comparison of GDF11 and myostatin protein expression between muscle and tumor. (G) ELISA-determined levels of GDF11 in GAS muscle and prostate tumor from sets of 4 mice, sham castrated (blue) or 2 weeks after castration (red), measured 3 times. (H) Representative immunoblots of MSTN in GAS muscle and prostate tumor from sets of 4 mice, sham-castrated or 8 weeks after castration. (I) Quantification of relative levels of MSTN between GAS muscle and prostate tumor. Columns are normalized means; bars are SEM. n = 4/group, indicated by open circles. *P < 0.05, **P < 0.01, and ***P < 0.001 versus sham-castrated group (except G and I, GAS muscle vs. tumor tissue), determined using 1-way ANOVA and Dunnett’s test (A, D, and G) or 1-way ANOVA and Bonferroni’s correction (C, F, and I).

Journal: JCI Insight

Article Title: Prostate tumor–derived GDF11 accelerates androgen deprivation therapy–induced sarcopenia

doi: 10.1172/jci.insight.127018

Figure Lengend Snippet: (A–C) GDF11 and myostatin protein expression in tumor. (A) ELISA-determined levels of GDF11 in prostate tumor tissue, from 4 mice at each time, measured 3 times. (B) Representative immunoblots of soluble active myostatin C-terminal dimer (MSTN) and eukaryotic elongation factor 2 (EF2) expression in prostate tumor tissue from sets of 4 mice, castrated for the indicated times or sham castrated. Lanes of immunoblots marked “C” contain identical control sample for interblot comparison. (C) Quantification of MSTN levels in tumor tissue from castrated (red) or sham-castrated (blue) mice, from 3 determinations for each tumor (see Supplemental Figure 5 for additional immunoblots and supplemental materials for full, uncut gels). (D–F) GDF11 and myostatin protein expression in serum. (D) ELISA-determined levels of GDF11 in serum, from 4 mice at each time, measured 3 times. (E) Representative immunoblots of MSTN expression in equal quantities of serum protein from the 4 mice in A. (F) Quantification of MSTN levels in serum, as in B. (G–I) Comparison of GDF11 and myostatin protein expression between muscle and tumor. (G) ELISA-determined levels of GDF11 in GAS muscle and prostate tumor from sets of 4 mice, sham castrated (blue) or 2 weeks after castration (red), measured 3 times. (H) Representative immunoblots of MSTN in GAS muscle and prostate tumor from sets of 4 mice, sham-castrated or 8 weeks after castration. (I) Quantification of relative levels of MSTN between GAS muscle and prostate tumor. Columns are normalized means; bars are SEM. n = 4/group, indicated by open circles. *P < 0.05, **P < 0.01, and ***P < 0.001 versus sham-castrated group (except G and I, GAS muscle vs. tumor tissue), determined using 1-way ANOVA and Dunnett’s test (A, D, and G) or 1-way ANOVA and Bonferroni’s correction (C, F, and I).

Article Snippet: ELISA kits used were human/mouse/rat activin A ELISA kit (Quantikine DAC00B, R&D Systems, Bio-Techne), mouse activin B ELISA kit (E15932m, Cusabio Biotech Co., Ltd.), mouse activin AB and mouse GDF11 ELISA kits (CEA158Mu and SEC113Mu, respectively, Cloud-Clone Corp.), and total myostatin ELISA kit (Quantikine DGDF80, R&D Systems, Bio-Techne).

Techniques: Expressing, Enzyme-linked Immunosorbent Assay, Western Blot, Control, Comparison

Graphs of castration-induced changes in myokine concentrations (colored lines) in skeletal muscle and serum of mice without prostate cancer (left side) or in skeletal muscle, serum, and tumor of mice with prostate cancer (right side). Tumor lobes are represented by the green (left lobe) and red (right lobe) circles. In adult tumor-free mice myostatin and the activins increase after castration but prior to strength and muscle mass loss. In PrCa tumor–bearing mice, tumor secretes GDF11 (blue) and later myostatin (red) into serum. Endocrine-derived GDF11 and myostatin increase in muscle prior to strength loss (early myostatin also moves from muscle into serum). The tumor-derived catabolic TGF-β family myokines exacerbate castration-induced sarcopenia in tumor-bearing mice.

Journal: JCI Insight

Article Title: Prostate tumor–derived GDF11 accelerates androgen deprivation therapy–induced sarcopenia

doi: 10.1172/jci.insight.127018

Figure Lengend Snippet: Graphs of castration-induced changes in myokine concentrations (colored lines) in skeletal muscle and serum of mice without prostate cancer (left side) or in skeletal muscle, serum, and tumor of mice with prostate cancer (right side). Tumor lobes are represented by the green (left lobe) and red (right lobe) circles. In adult tumor-free mice myostatin and the activins increase after castration but prior to strength and muscle mass loss. In PrCa tumor–bearing mice, tumor secretes GDF11 (blue) and later myostatin (red) into serum. Endocrine-derived GDF11 and myostatin increase in muscle prior to strength loss (early myostatin also moves from muscle into serum). The tumor-derived catabolic TGF-β family myokines exacerbate castration-induced sarcopenia in tumor-bearing mice.

Article Snippet: ELISA kits used were human/mouse/rat activin A ELISA kit (Quantikine DAC00B, R&D Systems, Bio-Techne), mouse activin B ELISA kit (E15932m, Cusabio Biotech Co., Ltd.), mouse activin AB and mouse GDF11 ELISA kits (CEA158Mu and SEC113Mu, respectively, Cloud-Clone Corp.), and total myostatin ELISA kit (Quantikine DGDF80, R&D Systems, Bio-Techne).

Techniques: Derivative Assay