fgf1 Search Results


goat polyclonal anti fgf1  (R&D Systems)
92
R&D Systems goat polyclonal anti fgf1
Goat Polyclonal Anti Fgf1, supplied by R&D Systems, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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acidic fibroblast growth factor  (R&D Systems Hematology)
94
R&D Systems Hematology acidic fibroblast growth factor
Acidic Fibroblast Growth Factor, supplied by R&D Systems Hematology, 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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bovine afgf  (R&D Systems)
90
R&D Systems bovine afgf
FIG. 1. Western blot analysis of porcine uterine protein extract at Day 12 of gestation. a) Molecular weight markers (x 10 3) (lane 1), total CM-50 sephadex-extracted uterine protein (25 g, lanes 2, 4, and 6), human recombinant bFGF (100 ng, lanes 3 and 5). Lanes 1 and 2 were stained for total protein by colloidal gold stain. Lanes 3 and 4 were in- cubated with anti-bFGF antibody (0.15 Ixg/ml). Lanes 5 and 6 were in- cubated with rabbit IgG (0.15 .Lg/ml). b) Sephadex-extracted uterine pro- tein (25 jIg, stained for total protein by colloidal gold) in nonreducing <t>7.5-15%</t> <t>PAGE.</t> Bovine <t>aFGF</t> (500 ng, lanes 2, 4, and 6) and sephadex extract (25 g, lanes 3, 5, and 7). Immunoreactive aFGF bands are ob- served in lanes 2 and 3 (incubated with anti-aFGF antibody). The absence of these bands is noted in lanes 4 and 5 (anti-aFGF antibody immunoab- sorbed with bovine aFGF) and in lanes 6 and 7 (incubated with rabbit IgG).
Bovine Afgf, supplied by R&D Systems, 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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recombinant mouse fgf1  (R&D Systems)
94
R&D Systems recombinant mouse fgf1
FIG. 1. Western blot analysis of porcine uterine protein extract at Day 12 of gestation. a) Molecular weight markers (x 10 3) (lane 1), total CM-50 sephadex-extracted uterine protein (25 g, lanes 2, 4, and 6), human recombinant bFGF (100 ng, lanes 3 and 5). Lanes 1 and 2 were stained for total protein by colloidal gold stain. Lanes 3 and 4 were in- cubated with anti-bFGF antibody (0.15 Ixg/ml). Lanes 5 and 6 were in- cubated with rabbit IgG (0.15 .Lg/ml). b) Sephadex-extracted uterine pro- tein (25 jIg, stained for total protein by colloidal gold) in nonreducing <t>7.5-15%</t> <t>PAGE.</t> Bovine <t>aFGF</t> (500 ng, lanes 2, 4, and 6) and sephadex extract (25 g, lanes 3, 5, and 7). Immunoreactive aFGF bands are ob- served in lanes 2 and 3 (incubated with anti-aFGF antibody). The absence of these bands is noted in lanes 4 and 5 (anti-aFGF antibody immunoab- sorbed with bovine aFGF) and in lanes 6 and 7 (incubated with rabbit IgG).
Recombinant Mouse Fgf1, supplied by R&D Systems, 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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rabbit polyclonal anti fgf1  (R&D Systems)
90
R&D Systems rabbit polyclonal anti fgf1
FIG. 1. Western blot analysis of porcine uterine protein extract at Day 12 of gestation. a) Molecular weight markers (x 10 3) (lane 1), total CM-50 sephadex-extracted uterine protein (25 g, lanes 2, 4, and 6), human recombinant bFGF (100 ng, lanes 3 and 5). Lanes 1 and 2 were stained for total protein by colloidal gold stain. Lanes 3 and 4 were in- cubated with anti-bFGF antibody (0.15 Ixg/ml). Lanes 5 and 6 were in- cubated with rabbit IgG (0.15 .Lg/ml). b) Sephadex-extracted uterine pro- tein (25 jIg, stained for total protein by colloidal gold) in nonreducing <t>7.5-15%</t> <t>PAGE.</t> Bovine <t>aFGF</t> (500 ng, lanes 2, 4, and 6) and sephadex extract (25 g, lanes 3, 5, and 7). Immunoreactive aFGF bands are ob- served in lanes 2 and 3 (incubated with anti-aFGF antibody). The absence of these bands is noted in lanes 4 and 5 (anti-aFGF antibody immunoab- sorbed with bovine aFGF) and in lanes 6 and 7 (incubated with rabbit IgG).
Rabbit Polyclonal Anti Fgf1, supplied by R&D Systems, 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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fgf 1 cat no 231 bc  (R&D Systems)
94
R&D Systems fgf 1 cat no 231 bc
FIG. 1. Western blot analysis of porcine uterine protein extract at Day 12 of gestation. a) Molecular weight markers (x 10 3) (lane 1), total CM-50 sephadex-extracted uterine protein (25 g, lanes 2, 4, and 6), human recombinant bFGF (100 ng, lanes 3 and 5). Lanes 1 and 2 were stained for total protein by colloidal gold stain. Lanes 3 and 4 were in- cubated with anti-bFGF antibody (0.15 Ixg/ml). Lanes 5 and 6 were in- cubated with rabbit IgG (0.15 .Lg/ml). b) Sephadex-extracted uterine pro- tein (25 jIg, stained for total protein by colloidal gold) in nonreducing <t>7.5-15%</t> <t>PAGE.</t> Bovine <t>aFGF</t> (500 ng, lanes 2, 4, and 6) and sephadex extract (25 g, lanes 3, 5, and 7). Immunoreactive aFGF bands are ob- served in lanes 2 and 3 (incubated with anti-aFGF antibody). The absence of these bands is noted in lanes 4 and 5 (anti-aFGF antibody immunoab- sorbed with bovine aFGF) and in lanes 6 and 7 (incubated with rabbit IgG).
Fgf 1 Cat No 231 Bc, supplied by R&D Systems, 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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human afgf elisa kit  (R&D Systems)
93
R&D Systems human afgf elisa kit
Dilution-ratio evaluation of tissue samples and establishment of a calibration curve. (A) Concentration of <t>rh-aFGF</t> quality-control (QC) samples, as calculated by the standard curve prepared with RD 6X buffer. “RD 6X” indicates the calibrator diluents of the commercial <t>ELISA</t> kit, which was diluted 10-fold with PBS buffer. “10×” indicates skin homogenate that was diluted 10-fold with PBS buffer. (B) Concentrations of rh-aFGF QC samples, as calculated by the standard curve prepared with 10× diluted skin homogenate. (C) Calibration curve for measurement of rh-aFGF levels in rat skin tissue homogenates ( n = 9). The red curve is the fitted standard curve. (D) Calibration curve for measurement of rh-aFGF levels in rat serum samples ( n = 8). The red curve is the fitted standard curve.
Human Afgf Elisa Kit, supplied by R&D Systems, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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human fgf acidic elisa kit  (R&D Systems)
93
R&D Systems human fgf acidic elisa kit
Dilution-ratio evaluation of tissue samples and establishment of a calibration curve. (A) Concentration of <t>rh-aFGF</t> quality-control (QC) samples, as calculated by the standard curve prepared with RD 6X buffer. “RD 6X” indicates the calibrator diluents of the commercial <t>ELISA</t> kit, which was diluted 10-fold with PBS buffer. “10×” indicates skin homogenate that was diluted 10-fold with PBS buffer. (B) Concentrations of rh-aFGF QC samples, as calculated by the standard curve prepared with 10× diluted skin homogenate. (C) Calibration curve for measurement of rh-aFGF levels in rat skin tissue homogenates ( n = 9). The red curve is the fitted standard curve. (D) Calibration curve for measurement of rh-aFGF levels in rat serum samples ( n = 8). The red curve is the fitted standard curve.
Human Fgf Acidic Elisa Kit, supplied by R&D Systems, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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polyclonal antibody baf232  (R&D Systems)
92
R&D Systems polyclonal antibody baf232
Dilution-ratio evaluation of tissue samples and establishment of a calibration curve. (A) Concentration of <t>rh-aFGF</t> quality-control (QC) samples, as calculated by the standard curve prepared with RD 6X buffer. “RD 6X” indicates the calibrator diluents of the commercial <t>ELISA</t> kit, which was diluted 10-fold with PBS buffer. “10×” indicates skin homogenate that was diluted 10-fold with PBS buffer. (B) Concentrations of rh-aFGF QC samples, as calculated by the standard curve prepared with 10× diluted skin homogenate. (C) Calibration curve for measurement of rh-aFGF levels in rat skin tissue homogenates ( n = 9). The red curve is the fitted standard curve. (D) Calibration curve for measurement of rh-aFGF levels in rat serum samples ( n = 8). The red curve is the fitted standard curve.
Polyclonal Antibody Baf232, supplied by R&D Systems, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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r d recombinant human fgf acidic aa  (R&D Systems)
90
R&D Systems r d recombinant human fgf acidic aa
Dilution-ratio evaluation of tissue samples and establishment of a calibration curve. (A) Concentration of <t>rh-aFGF</t> quality-control (QC) samples, as calculated by the standard curve prepared with RD 6X buffer. “RD 6X” indicates the calibrator diluents of the commercial <t>ELISA</t> kit, which was diluted 10-fold with PBS buffer. “10×” indicates skin homogenate that was diluted 10-fold with PBS buffer. (B) Concentrations of rh-aFGF QC samples, as calculated by the standard curve prepared with 10× diluted skin homogenate. (C) Calibration curve for measurement of rh-aFGF levels in rat skin tissue homogenates ( n = 9). The red curve is the fitted standard curve. (D) Calibration curve for measurement of rh-aFGF levels in rat serum samples ( n = 8). The red curve is the fitted standard curve.
R D Recombinant Human Fgf Acidic Aa, supplied by R&D Systems, 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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recombinant acidic human fibroblast growth factor 1  (R&D Systems)
91
R&D Systems recombinant acidic human fibroblast growth factor 1
Dilution-ratio evaluation of tissue samples and establishment of a calibration curve. (A) Concentration of <t>rh-aFGF</t> quality-control (QC) samples, as calculated by the standard curve prepared with RD 6X buffer. “RD 6X” indicates the calibrator diluents of the commercial <t>ELISA</t> kit, which was diluted 10-fold with PBS buffer. “10×” indicates skin homogenate that was diluted 10-fold with PBS buffer. (B) Concentrations of rh-aFGF QC samples, as calculated by the standard curve prepared with 10× diluted skin homogenate. (C) Calibration curve for measurement of rh-aFGF levels in rat skin tissue homogenates ( n = 9). The red curve is the fitted standard curve. (D) Calibration curve for measurement of rh-aFGF levels in rat serum samples ( n = 8). The red curve is the fitted standard curve.
Recombinant Acidic Human Fibroblast Growth Factor 1, supplied by R&D Systems, 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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Image Search Results


FIG. 1. Western blot analysis of porcine uterine protein extract at Day 12 of gestation. a) Molecular weight markers (x 10 3) (lane 1), total CM-50 sephadex-extracted uterine protein (25 g, lanes 2, 4, and 6), human recombinant bFGF (100 ng, lanes 3 and 5). Lanes 1 and 2 were stained for total protein by colloidal gold stain. Lanes 3 and 4 were in- cubated with anti-bFGF antibody (0.15 Ixg/ml). Lanes 5 and 6 were in- cubated with rabbit IgG (0.15 .Lg/ml). b) Sephadex-extracted uterine pro- tein (25 jIg, stained for total protein by colloidal gold) in nonreducing 7.5-15% PAGE. Bovine aFGF (500 ng, lanes 2, 4, and 6) and sephadex extract (25 g, lanes 3, 5, and 7). Immunoreactive aFGF bands are ob- served in lanes 2 and 3 (incubated with anti-aFGF antibody). The absence of these bands is noted in lanes 4 and 5 (anti-aFGF antibody immunoab- sorbed with bovine aFGF) and in lanes 6 and 7 (incubated with rabbit IgG).

Journal: Biology of reproduction

Article Title: Immunolocalization of acidic and basic fibroblast growth factors in porcine uterine and conceptus tissues.

doi: 10.1095/biolreprod56.6.1527

Figure Lengend Snippet: FIG. 1. Western blot analysis of porcine uterine protein extract at Day 12 of gestation. a) Molecular weight markers (x 10 3) (lane 1), total CM-50 sephadex-extracted uterine protein (25 g, lanes 2, 4, and 6), human recombinant bFGF (100 ng, lanes 3 and 5). Lanes 1 and 2 were stained for total protein by colloidal gold stain. Lanes 3 and 4 were in- cubated with anti-bFGF antibody (0.15 Ixg/ml). Lanes 5 and 6 were in- cubated with rabbit IgG (0.15 .Lg/ml). b) Sephadex-extracted uterine pro- tein (25 jIg, stained for total protein by colloidal gold) in nonreducing 7.5-15% PAGE. Bovine aFGF (500 ng, lanes 2, 4, and 6) and sephadex extract (25 g, lanes 3, 5, and 7). Immunoreactive aFGF bands are ob- served in lanes 2 and 3 (incubated with anti-aFGF antibody). The absence of these bands is noted in lanes 4 and 5 (anti-aFGF antibody immunoab- sorbed with bovine aFGF) and in lanes 6 and 7 (incubated with rabbit IgG).

Article Snippet: For aFGE PAGE was performed using 7.5-15% acrylamide gel and bovine aFGF (cat. #132-FA; R&D Systems, Minneapolis, MN) as standard.

Techniques: Western Blot, Molecular Weight, Recombinant, Staining, Incubation

Dilution-ratio evaluation of tissue samples and establishment of a calibration curve. (A) Concentration of rh-aFGF quality-control (QC) samples, as calculated by the standard curve prepared with RD 6X buffer. “RD 6X” indicates the calibrator diluents of the commercial ELISA kit, which was diluted 10-fold with PBS buffer. “10×” indicates skin homogenate that was diluted 10-fold with PBS buffer. (B) Concentrations of rh-aFGF QC samples, as calculated by the standard curve prepared with 10× diluted skin homogenate. (C) Calibration curve for measurement of rh-aFGF levels in rat skin tissue homogenates ( n = 9). The red curve is the fitted standard curve. (D) Calibration curve for measurement of rh-aFGF levels in rat serum samples ( n = 8). The red curve is the fitted standard curve.

Journal: Frontiers in Pharmacology

Article Title: Validation of a Double-Sandwich Enzyme-Linked Immunoassay for Pharmacokinetic Study of an rh-aFGF Hydrogel in Rat Skin and Serum

doi: 10.3389/fphar.2020.00700

Figure Lengend Snippet: Dilution-ratio evaluation of tissue samples and establishment of a calibration curve. (A) Concentration of rh-aFGF quality-control (QC) samples, as calculated by the standard curve prepared with RD 6X buffer. “RD 6X” indicates the calibrator diluents of the commercial ELISA kit, which was diluted 10-fold with PBS buffer. “10×” indicates skin homogenate that was diluted 10-fold with PBS buffer. (B) Concentrations of rh-aFGF QC samples, as calculated by the standard curve prepared with 10× diluted skin homogenate. (C) Calibration curve for measurement of rh-aFGF levels in rat skin tissue homogenates ( n = 9). The red curve is the fitted standard curve. (D) Calibration curve for measurement of rh-aFGF levels in rat serum samples ( n = 8). The red curve is the fitted standard curve.

Article Snippet: Commercial rh-aFGF for external use (rh-aFGF-Ai) was provided by Shanghai Tenry Pharmaceutical Company Ltd. Recombinant human insulin was provided by Liaoning Boao Biopharmaceutical Co., Ltd. RD6X buffer and Human aFGF ELISA Kit were purchased from R&D System (USA, code number was DFA00B and batch number was P155336).

Techniques: Concentration Assay, Control, Enzyme-linked Immunosorbent Assay

Evaluation of precision and accuracy of the double-sandwich enzyme-linked immunosorbent assay (ELISA) method. (A) Within-batch precision and accuracy of rh-aFGF in skin homogenate ( n = 5). (B) Within-batch precision and accuracy of rh-aFGF in serum ( n = 5). (C) Inter-batch precision and accuracy of rh-aFGF in skin homogenate ( n = 6). (D) Inter-batch precision and accuracy of rh-aFGF in serum ( n = 6).

Journal: Frontiers in Pharmacology

Article Title: Validation of a Double-Sandwich Enzyme-Linked Immunoassay for Pharmacokinetic Study of an rh-aFGF Hydrogel in Rat Skin and Serum

doi: 10.3389/fphar.2020.00700

Figure Lengend Snippet: Evaluation of precision and accuracy of the double-sandwich enzyme-linked immunosorbent assay (ELISA) method. (A) Within-batch precision and accuracy of rh-aFGF in skin homogenate ( n = 5). (B) Within-batch precision and accuracy of rh-aFGF in serum ( n = 5). (C) Inter-batch precision and accuracy of rh-aFGF in skin homogenate ( n = 6). (D) Inter-batch precision and accuracy of rh-aFGF in serum ( n = 6).

Article Snippet: Commercial rh-aFGF for external use (rh-aFGF-Ai) was provided by Shanghai Tenry Pharmaceutical Company Ltd. Recombinant human insulin was provided by Liaoning Boao Biopharmaceutical Co., Ltd. RD6X buffer and Human aFGF ELISA Kit were purchased from R&D System (USA, code number was DFA00B and batch number was P155336).

Techniques: Sandwich ELISA, Enzyme-linked Immunosorbent Assay

Specificity of the double-sandwich enzyme-linked immunosorbent assay (ELISA) method. (A) bFGF. (B) FGF-21. (C) KGF-2. (D) Insulin.

Journal: Frontiers in Pharmacology

Article Title: Validation of a Double-Sandwich Enzyme-Linked Immunoassay for Pharmacokinetic Study of an rh-aFGF Hydrogel in Rat Skin and Serum

doi: 10.3389/fphar.2020.00700

Figure Lengend Snippet: Specificity of the double-sandwich enzyme-linked immunosorbent assay (ELISA) method. (A) bFGF. (B) FGF-21. (C) KGF-2. (D) Insulin.

Article Snippet: Commercial rh-aFGF for external use (rh-aFGF-Ai) was provided by Shanghai Tenry Pharmaceutical Company Ltd. Recombinant human insulin was provided by Liaoning Boao Biopharmaceutical Co., Ltd. RD6X buffer and Human aFGF ELISA Kit were purchased from R&D System (USA, code number was DFA00B and batch number was P155336).

Techniques: Sandwich ELISA, Enzyme-linked Immunosorbent Assay

Stability of rh-aFGF samples stored under different conditions. (A) Stabilities of rh-aFGF HQC samples (3200 pg/mL) in skin homogenates ( n = 5). (B) Stabilities of rh-aFGF LQC samples (160 pg/mL) in skin homogenates ( n = 5). (C) Stabilities of rh-aFGF HQC samples (3200 pg/mL) in sera ( n = 5). (D) Stabilities of rh-aFGF LQC samples (160 pg/mL) in sera ( n = 5) from the following: (1) after 2°C to 8°C for 1 day; (2) after being at room temperature for 3 h; (3) after one freeze–thaw cycle; (4) after two freeze–thaw cycles; (5) after long-term storage at −80°C for 24 days; or (6) after long-term storage at −80°C for 55 days.

Journal: Frontiers in Pharmacology

Article Title: Validation of a Double-Sandwich Enzyme-Linked Immunoassay for Pharmacokinetic Study of an rh-aFGF Hydrogel in Rat Skin and Serum

doi: 10.3389/fphar.2020.00700

Figure Lengend Snippet: Stability of rh-aFGF samples stored under different conditions. (A) Stabilities of rh-aFGF HQC samples (3200 pg/mL) in skin homogenates ( n = 5). (B) Stabilities of rh-aFGF LQC samples (160 pg/mL) in skin homogenates ( n = 5). (C) Stabilities of rh-aFGF HQC samples (3200 pg/mL) in sera ( n = 5). (D) Stabilities of rh-aFGF LQC samples (160 pg/mL) in sera ( n = 5) from the following: (1) after 2°C to 8°C for 1 day; (2) after being at room temperature for 3 h; (3) after one freeze–thaw cycle; (4) after two freeze–thaw cycles; (5) after long-term storage at −80°C for 24 days; or (6) after long-term storage at −80°C for 55 days.

Article Snippet: Commercial rh-aFGF for external use (rh-aFGF-Ai) was provided by Shanghai Tenry Pharmaceutical Company Ltd. Recombinant human insulin was provided by Liaoning Boao Biopharmaceutical Co., Ltd. RD6X buffer and Human aFGF ELISA Kit were purchased from R&D System (USA, code number was DFA00B and batch number was P155336).

Techniques: