anti gap dh Search Results


gap dh  (Santa Cruz Biotechnology)
97
Santa Cruz Biotechnology gap dh
L1CAM mRNA and protein levels in endometrial carcinoma cell lines overexpresssing transcription <t>factors</t> <t>β-catenin</t> or Slug . ( A ) Regulation of L1CAM expression after transfection of a point mutated, constitutively active form of β-catenin (S33Y) or control pcDNA3 plasmid as determined by qRT-PCR using specific primers. ( B ) Regulation of L1CAM levels after overexpression of a HA-SLUG or control plasmid. Means ± SD from n = 3 independent experiments are shown. ( C ) Western blot analysis for L1CAM and β-catenin as well as <t>GAP-DH,</t> used as a loading control. ( D ) Western blot analysis for L1CAM and anti SLUG as well as GAP-DH, used as a loading control. A representative experiment from n = 3 is shown.
Gap Dh, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/anti+gap+dh/GAPDH+Antibody/pmc02939505-62-15-17
Average 97 stars, based on 1 article reviews
gap dh - by Bioz Stars, 2026-10
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anti glyceraldehyde phosphate dehydrogenase  (Biosynth Carbosynth)
95
Biosynth Carbosynth anti glyceraldehyde phosphate dehydrogenase
L1CAM mRNA and protein levels in endometrial carcinoma cell lines overexpresssing transcription <t>factors</t> <t>β-catenin</t> or Slug . ( A ) Regulation of L1CAM expression after transfection of a point mutated, constitutively active form of β-catenin (S33Y) or control pcDNA3 plasmid as determined by qRT-PCR using specific primers. ( B ) Regulation of L1CAM levels after overexpression of a HA-SLUG or control plasmid. Means ± SD from n = 3 independent experiments are shown. ( C ) Western blot analysis for L1CAM and β-catenin as well as <t>GAP-DH,</t> used as a loading control. ( D ) Western blot analysis for L1CAM and anti SLUG as well as GAP-DH, used as a loading control. A representative experiment from n = 3 is shown.
Anti Glyceraldehyde Phosphate Dehydrogenase, supplied by Biosynth Carbosynth, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/anti+gap+dh/GAPDH+antibody/pm30541771-162-28-35
Average 95 stars, based on 1 article reviews
anti glyceraldehyde phosphate dehydrogenase - by Bioz Stars, 2026-10
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primary antibodies  (Santa Cruz Biotechnology)
96
Santa Cruz Biotechnology primary antibodies
L1CAM mRNA and protein levels in endometrial carcinoma cell lines overexpresssing transcription <t>factors</t> <t>β-catenin</t> or Slug . ( A ) Regulation of L1CAM expression after transfection of a point mutated, constitutively active form of β-catenin (S33Y) or control pcDNA3 plasmid as determined by qRT-PCR using specific primers. ( B ) Regulation of L1CAM levels after overexpression of a HA-SLUG or control plasmid. Means ± SD from n = 3 independent experiments are shown. ( C ) Western blot analysis for L1CAM and β-catenin as well as <t>GAP-DH,</t> used as a loading control. ( D ) Western blot analysis for L1CAM and anti SLUG as well as GAP-DH, used as a loading control. A representative experiment from n = 3 is shown.
Primary Antibodies, supplied by Santa Cruz Biotechnology, 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/product/anti+gap+dh/GFAP+Antibody/pm30268884-111-12-15
Average 96 stars, based on 1 article reviews
primary antibodies - by Bioz Stars, 2026-10
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mouse α gap dh  (Merck & Co)
86
Merck & Co mouse α gap dh
L1CAM mRNA and protein levels in endometrial carcinoma cell lines overexpresssing transcription <t>factors</t> <t>β-catenin</t> or Slug . ( A ) Regulation of L1CAM expression after transfection of a point mutated, constitutively active form of β-catenin (S33Y) or control pcDNA3 plasmid as determined by qRT-PCR using specific primers. ( B ) Regulation of L1CAM levels after overexpression of a HA-SLUG or control plasmid. Means ± SD from n = 3 independent experiments are shown. ( C ) Western blot analysis for L1CAM and β-catenin as well as <t>GAP-DH,</t> used as a loading control. ( D ) Western blot analysis for L1CAM and anti SLUG as well as GAP-DH, used as a loading control. A representative experiment from n = 3 is shown.
Mouse α Gap Dh, supplied by Merck & Co, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 86 stars, based on 1 article reviews
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gap dh  (Danaher Inc)
99
Danaher Inc gap dh
Fig. 4. miR-124-mediated repression of fibronectin binding is dependent on integrin expression profile. SCC4 cells (A) or the ITGB6 deficient H357 (B–D) were transfected with miR-124, siRNA <t>targeting</t> <t>ITGB1</t> (si-ITGB1) or negative control scrambled oligonucleotide. Cells were assayed for their ability to adhere to fibronectin (A, B, and D) or immunoblotted for ITGB1. (C) 24 h post transfection, as described in Section 2. Data presented represents the number of adherent cells normalised to mock transfection or densitometrical analysis of immunoblots relative to <t>GAP-DH</t> ± S.E.M. (n P 3, * = P < 0.01 by Mann–Whitney U test).
Gap Dh, supplied by Danaher Inc, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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gapdh antibody 1d4 dylight 755  (Novus Biologicals)
N/A
The GAPDH Antibody 1D4 DyLight 755 from Novus Biologicals is a mouse monoclonal antibody to GAPDH This antibody reacts with human mouse rat porcine avian bovine chicken equine hamster opossum primate sheep zebrafish The GAPDH
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gapdh antibody nb615 dylight 488  (Novus Biologicals)
N/A
The GAPDH Antibody NB615 DyLight 488 from Novus Biologicals is a mouse monoclonal antibody to GAPDH This antibody reacts with human mouse rat porcine bovine canine chicken rabbit The GAPDH Antibody NB615 DyLight 488 has
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gapdh antibody nb615 dylight 405  (Novus Biologicals)
N/A
The GAPDH Antibody NB615 DyLight 405 from Novus Biologicals is a mouse monoclonal antibody to GAPDH This antibody reacts with human mouse rat porcine bovine canine chicken rabbit The GAPDH Antibody NB615 DyLight 405 has
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gapdh antibody 2d4a7 dylight 755  (Novus Biologicals)
N/A
The GAPDH Antibody 2D4A7 DyLight 755 from Novus Biologicals is a mouse monoclonal antibody to GAPDH This antibody reacts with human mouse rat porcine rabbit The GAPDH Antibody 2D4A7 DyLight 755 has been validated for
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gapdh antibody  (Biosynth Carbosynth)
N/A
Mouse monoclonal GAPDH antibody
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Image Search Results


L1CAM mRNA and protein levels in endometrial carcinoma cell lines overexpresssing transcription factors β-catenin or Slug . ( A ) Regulation of L1CAM expression after transfection of a point mutated, constitutively active form of β-catenin (S33Y) or control pcDNA3 plasmid as determined by qRT-PCR using specific primers. ( B ) Regulation of L1CAM levels after overexpression of a HA-SLUG or control plasmid. Means ± SD from n = 3 independent experiments are shown. ( C ) Western blot analysis for L1CAM and β-catenin as well as GAP-DH, used as a loading control. ( D ) Western blot analysis for L1CAM and anti SLUG as well as GAP-DH, used as a loading control. A representative experiment from n = 3 is shown.

Journal: BMC Molecular Biology

Article Title: L1CAM expression in endometrial carcinomas is regulated by usage of two different promoter regions

doi: 10.1186/1471-2199-11-64

Figure Lengend Snippet: L1CAM mRNA and protein levels in endometrial carcinoma cell lines overexpresssing transcription factors β-catenin or Slug . ( A ) Regulation of L1CAM expression after transfection of a point mutated, constitutively active form of β-catenin (S33Y) or control pcDNA3 plasmid as determined by qRT-PCR using specific primers. ( B ) Regulation of L1CAM levels after overexpression of a HA-SLUG or control plasmid. Means ± SD from n = 3 independent experiments are shown. ( C ) Western blot analysis for L1CAM and β-catenin as well as GAP-DH, used as a loading control. ( D ) Western blot analysis for L1CAM and anti SLUG as well as GAP-DH, used as a loading control. A representative experiment from n = 3 is shown.

Article Snippet: Antibodies for detection in Western blot against β-catenin were from Sigma-Aldrich (Schnelldorf, Germany) and against GAP-DH from SantaCruz Biotechnology (Heidelberg, Germany).

Techniques: Expressing, Transfection, Control, Plasmid Preparation, Quantitative RT-PCR, Over Expression, Western Blot

Fig. 4. miR-124-mediated repression of fibronectin binding is dependent on integrin expression profile. SCC4 cells (A) or the ITGB6 deficient H357 (B–D) were transfected with miR-124, siRNA targeting ITGB1 (si-ITGB1) or negative control scrambled oligonucleotide. Cells were assayed for their ability to adhere to fibronectin (A, B, and D) or immunoblotted for ITGB1. (C) 24 h post transfection, as described in Section 2. Data presented represents the number of adherent cells normalised to mock transfection or densitometrical analysis of immunoblots relative to GAP-DH ± S.E.M. (n P 3, * = P < 0.01 by Mann–Whitney U test).

Journal: FEBS letters

Article Title: MicroRNA-124 suppresses oral squamous cell carcinoma motility by targeting ITGB1.

doi: 10.1016/j.febslet.2010.11.038

Figure Lengend Snippet: Fig. 4. miR-124-mediated repression of fibronectin binding is dependent on integrin expression profile. SCC4 cells (A) or the ITGB6 deficient H357 (B–D) were transfected with miR-124, siRNA targeting ITGB1 (si-ITGB1) or negative control scrambled oligonucleotide. Cells were assayed for their ability to adhere to fibronectin (A, B, and D) or immunoblotted for ITGB1. (C) 24 h post transfection, as described in Section 2. Data presented represents the number of adherent cells normalised to mock transfection or densitometrical analysis of immunoblots relative to GAP-DH ± S.E.M. (n P 3, * = P < 0.01 by Mann–Whitney U test).

Article Snippet: Following blocking of non-specific protein binding, membranes were incubated with antibodies directed to ITGB1 (1:1000, Millipore), GAP-DH (1:2000, Abcam) or b-actin (1:10,000, Sigma).

Techniques: Binding Assay, Expressing, Transfection, Negative Control, Western Blot, MANN-WHITNEY