efna5 antibody Search Results


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Produced in rabbits immunized with purified recombinant Human EphrinA5 rhEphrinA5 Catalog 10192 H08H NP 001953 1 Met 1 Asn 203 EphrinA5 specific IgG was purified by human EphrinA5 affinity chromatography
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OriGene efna5 protein expression analysis
<t>EFNA5</t> expression is associated with good prognosis in hepatoma. A TCGA analysis of EFNA5 expression difference between liver tumor tissue and normal liver tissue. ** P < 0.01. B KM-plotter analysis of connection between EFNA5 expression and prognosis in hepatoma. C STRING online analysis of EFNA5 and related genes. D GO enrichment analysis of differential genes in hepatoma. E KEGG enrichment analysis of differential genes in hepatoma. F , G Representative IHC images and average density scores of EFNA5 expression in hepatoma and adjacent tissues
Efna5 Protein Expression Analysis, supplied by OriGene, 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/product/efna5+antibody/Ephrin+A5+(EFNA5)+Rabbit+Polyclonal+Antibody/pmc11489415-87-12-19
Average 92 stars, based on 1 article reviews
efna5 protein expression analysis - by Bioz Stars, 2026-10
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Atlas Antibodies efna5
<t>EfnA5</t> gene expression levels are reduced in SOD1 G93A mice whereas efnA5 protein is not altered in ALS patients CSF. a EfnA5 gene expression was determined in the lumbar spinal cord of SOD1 WT and SOD1 G93A overexpressing mice ( N = 4–9). Data represents mean ± SEM, and different conditions were compared with a two-way ANOVA with Tukey’s multiple comparisons test: ** P < 0.01 as compared with SOD1 WT . b EfnA5 protein relative quantification in the CSF of patients carrying an ALS genetic known mutation (gALS) and patients without any known mutation (sALS) were compared to the levels found in the CSF of young and aged controls (Con) and asymptomatic ALS patients carrying a known mutation for the disease (asympt ALS). Boxes show median and interquartile range, and whiskers are minimum and maximum. The light-to-heavy (L/H) peptide ratio was used as relative quantification of EfnA5 protein
Efna5, supplied by Atlas Antibodies, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/efna5+antibody/Anti-EFNA5/pmc06626434-110-7-28
Average 90 stars, based on 1 article reviews
efna5 - by Bioz Stars, 2026-10
90/100 stars
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Abnova anti-efna5 antibody h00001946-m02
<t>EfnA5</t> gene expression levels are reduced in SOD1 G93A mice whereas efnA5 protein is not altered in ALS patients CSF. a EfnA5 gene expression was determined in the lumbar spinal cord of SOD1 WT and SOD1 G93A overexpressing mice ( N = 4–9). Data represents mean ± SEM, and different conditions were compared with a two-way ANOVA with Tukey’s multiple comparisons test: ** P < 0.01 as compared with SOD1 WT . b EfnA5 protein relative quantification in the CSF of patients carrying an ALS genetic known mutation (gALS) and patients without any known mutation (sALS) were compared to the levels found in the CSF of young and aged controls (Con) and asymptomatic ALS patients carrying a known mutation for the disease (asympt ALS). Boxes show median and interquartile range, and whiskers are minimum and maximum. The light-to-heavy (L/H) peptide ratio was used as relative quantification of EfnA5 protein
Anti Efna5 Antibody H00001946 M02, supplied by Abnova, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/efna5+antibody/anti+efna5+antibody+h00001946+m02/pm38258903-142-3-5
Average 90 stars, based on 1 article reviews
anti-efna5 antibody h00001946-m02 - by Bioz Stars, 2026-10
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ImmunoWay Biotechnology Company anti-efna5 primary antibody
<t>EfnA5</t> gene expression levels are reduced in SOD1 G93A mice whereas efnA5 protein is not altered in ALS patients CSF. a EfnA5 gene expression was determined in the lumbar spinal cord of SOD1 WT and SOD1 G93A overexpressing mice ( N = 4–9). Data represents mean ± SEM, and different conditions were compared with a two-way ANOVA with Tukey’s multiple comparisons test: ** P < 0.01 as compared with SOD1 WT . b EfnA5 protein relative quantification in the CSF of patients carrying an ALS genetic known mutation (gALS) and patients without any known mutation (sALS) were compared to the levels found in the CSF of young and aged controls (Con) and asymptomatic ALS patients carrying a known mutation for the disease (asympt ALS). Boxes show median and interquartile range, and whiskers are minimum and maximum. The light-to-heavy (L/H) peptide ratio was used as relative quantification of EfnA5 protein
Anti Efna5 Primary Antibody, supplied by ImmunoWay Biotechnology Company, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/efna5+antibody/anti+efna5+primary+antibody/ppr0640133-71-13-18
Average 90 stars, based on 1 article reviews
anti-efna5 primary antibody - by Bioz Stars, 2026-10
90/100 stars
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EFNA5 rabbit polyclonal antibody
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Ephrin A5 EFNA5 189 200 goat polyclonal antibody Aff Purified
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Rabbit anti-Rat Efna5 Polyclonal Antibody
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Ephrin-A5, a member of the ephrin gene family, prevents axon bundling in cocultures of cortical neurons with astrocytes, a model of late stage nervous system development and differentiation. The EPH and EPH-related receptors comprise the
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Cell surface GPI-bound ligand for Eph receptors, a family of receptor tyrosine kinases which are crucial for migration, repulsion and adhesion during neuronal, vascular and epithelial development. Binds promiscuously Eph receptors residing on adjacent cells,
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Image Search Results


EFNA5 expression is associated with good prognosis in hepatoma. A TCGA analysis of EFNA5 expression difference between liver tumor tissue and normal liver tissue. ** P < 0.01. B KM-plotter analysis of connection between EFNA5 expression and prognosis in hepatoma. C STRING online analysis of EFNA5 and related genes. D GO enrichment analysis of differential genes in hepatoma. E KEGG enrichment analysis of differential genes in hepatoma. F , G Representative IHC images and average density scores of EFNA5 expression in hepatoma and adjacent tissues

Journal: Discover Oncology

Article Title: EFNA5 suppresses cell proliferation and tumor metastasis in hepatoma via epithelial-to-mesenchymal transition

doi: 10.1007/s12672-024-01454-7

Figure Lengend Snippet: EFNA5 expression is associated with good prognosis in hepatoma. A TCGA analysis of EFNA5 expression difference between liver tumor tissue and normal liver tissue. ** P < 0.01. B KM-plotter analysis of connection between EFNA5 expression and prognosis in hepatoma. C STRING online analysis of EFNA5 and related genes. D GO enrichment analysis of differential genes in hepatoma. E KEGG enrichment analysis of differential genes in hepatoma. F , G Representative IHC images and average density scores of EFNA5 expression in hepatoma and adjacent tissues

Article Snippet: In line with the manufacturer’s instruction, the IHC test kit (PV-6000) for EFNA5 protein expression analysis was bought from ZsBio (Beijing, China) and used.

Techniques: Expressing

EFNA5 inhibits the proliferation of hepatoma cells. A EFNA5 expression in hepatoma cell lines and normal hepatic epithelial cell line at the RNA levels by quantitative real-time PCR. *** P < 0.001. B Expression of EFNA5 in EFNA5-overexpressing HepG2 and LM3 cells, as detected by quantitative real-time PCR assays. C , D The proliferation ability of EFNA5 overexpressed hepatoma cells in LM3 and HepG2 cells was measured by CCK-8 method compared with the control group

Journal: Discover Oncology

Article Title: EFNA5 suppresses cell proliferation and tumor metastasis in hepatoma via epithelial-to-mesenchymal transition

doi: 10.1007/s12672-024-01454-7

Figure Lengend Snippet: EFNA5 inhibits the proliferation of hepatoma cells. A EFNA5 expression in hepatoma cell lines and normal hepatic epithelial cell line at the RNA levels by quantitative real-time PCR. *** P < 0.001. B Expression of EFNA5 in EFNA5-overexpressing HepG2 and LM3 cells, as detected by quantitative real-time PCR assays. C , D The proliferation ability of EFNA5 overexpressed hepatoma cells in LM3 and HepG2 cells was measured by CCK-8 method compared with the control group

Article Snippet: In line with the manufacturer’s instruction, the IHC test kit (PV-6000) for EFNA5 protein expression analysis was bought from ZsBio (Beijing, China) and used.

Techniques: Expressing, Real-time Polymerase Chain Reaction, CCK-8 Assay, Control

EFNA5 can inhibit the migration and invasion of hepatoma cells. A , B Representative images and quantitative analysis of cell migration based on Transwell assays. C , D The representative images and quantitative dat of the EdU assay in HepG2 and LM3

Journal: Discover Oncology

Article Title: EFNA5 suppresses cell proliferation and tumor metastasis in hepatoma via epithelial-to-mesenchymal transition

doi: 10.1007/s12672-024-01454-7

Figure Lengend Snippet: EFNA5 can inhibit the migration and invasion of hepatoma cells. A , B Representative images and quantitative analysis of cell migration based on Transwell assays. C , D The representative images and quantitative dat of the EdU assay in HepG2 and LM3

Article Snippet: In line with the manufacturer’s instruction, the IHC test kit (PV-6000) for EFNA5 protein expression analysis was bought from ZsBio (Beijing, China) and used.

Techniques: Migration, EdU Assay

EFNA5 inhibits EMT in hepatoma cells. A – C Analysis of epithelial–mesenchymal transition markers by western blotting and quantitative analysis in EFNA5 overexpression cell lysates. Overexpression of EFNA5 suppressed the protein levels of GAPDH, c-Myc, c-Jun, E-cadherin, N-cadherin, VIM, EGFR, and EFNA5 in HepG2 and LM3 cells

Journal: Discover Oncology

Article Title: EFNA5 suppresses cell proliferation and tumor metastasis in hepatoma via epithelial-to-mesenchymal transition

doi: 10.1007/s12672-024-01454-7

Figure Lengend Snippet: EFNA5 inhibits EMT in hepatoma cells. A – C Analysis of epithelial–mesenchymal transition markers by western blotting and quantitative analysis in EFNA5 overexpression cell lysates. Overexpression of EFNA5 suppressed the protein levels of GAPDH, c-Myc, c-Jun, E-cadherin, N-cadherin, VIM, EGFR, and EFNA5 in HepG2 and LM3 cells

Article Snippet: In line with the manufacturer’s instruction, the IHC test kit (PV-6000) for EFNA5 protein expression analysis was bought from ZsBio (Beijing, China) and used.

Techniques: Western Blot, Over Expression

EfnA5 gene expression levels are reduced in SOD1 G93A mice whereas efnA5 protein is not altered in ALS patients CSF. a EfnA5 gene expression was determined in the lumbar spinal cord of SOD1 WT and SOD1 G93A overexpressing mice ( N = 4–9). Data represents mean ± SEM, and different conditions were compared with a two-way ANOVA with Tukey’s multiple comparisons test: ** P < 0.01 as compared with SOD1 WT . b EfnA5 protein relative quantification in the CSF of patients carrying an ALS genetic known mutation (gALS) and patients without any known mutation (sALS) were compared to the levels found in the CSF of young and aged controls (Con) and asymptomatic ALS patients carrying a known mutation for the disease (asympt ALS). Boxes show median and interquartile range, and whiskers are minimum and maximum. The light-to-heavy (L/H) peptide ratio was used as relative quantification of EfnA5 protein

Journal: Acta Neuropathologica Communications

Article Title: Reduction of ephrin-A5 aggravates disease progression in amyotrophic lateral sclerosis

doi: 10.1186/s40478-019-0759-6

Figure Lengend Snippet: EfnA5 gene expression levels are reduced in SOD1 G93A mice whereas efnA5 protein is not altered in ALS patients CSF. a EfnA5 gene expression was determined in the lumbar spinal cord of SOD1 WT and SOD1 G93A overexpressing mice ( N = 4–9). Data represents mean ± SEM, and different conditions were compared with a two-way ANOVA with Tukey’s multiple comparisons test: ** P < 0.01 as compared with SOD1 WT . b EfnA5 protein relative quantification in the CSF of patients carrying an ALS genetic known mutation (gALS) and patients without any known mutation (sALS) were compared to the levels found in the CSF of young and aged controls (Con) and asymptomatic ALS patients carrying a known mutation for the disease (asympt ALS). Boxes show median and interquartile range, and whiskers are minimum and maximum. The light-to-heavy (L/H) peptide ratio was used as relative quantification of EfnA5 protein

Article Snippet: For multiple reaction monitoring (MRM) analysis of efnA5 in CSF samples, 200 μL of CSF were spiked with TEAB buffer and a quantitative protein epitope signature tag (QPrEST, Atlas Antibodies AB, #QPrEST25042) of efnA5 as internal standard.

Techniques: Gene Expression, Quantitative Proteomics, Mutagenesis

In the ventral horn of the spinal cord EfnA5 is mainly expressed in neurons. RNAscope in situ hybridization was performed to determine cell type-specific expression of EfnA5 . A total of 15–18 images of different lumbar spinal cord ventral horns from 3 different mice were analysed for every condition. a Representative images show lumbar spinal cord ventral horns of SOD1 WT and SOD1 G93A mice at 135 days of age that were stained with probes against EfnA5, Syp and Slc1a3 . Hoechst was used as a counter stain for nuclei. Scale bar = 50 μm. b Percentage of neurons ( Syp + cells) that stained positive for EfnA5 were quantified and shown as percentage of the total Syp + cells. c Glial cells ( Syp - cells) and d astrocytes ( Syp -, Slc1a3 + cells) positive for EfnA5 were quantified and represented as percentage of the total amount of glial cells. Single-cell EfnA5 expression was quantified by measuring EfnA5 puncta density (dots/μm 2 ) in e neurons, f glial cells and g astrocytes. Data represents mean ± SEM, and different conditions were compared with a two-tailed t-test: * P < 0.05; ** P < 0.01 as compared to SOD1 WT . b and e Data represents mean ± SEM, and different conditions were compared with a two-way ANOVA with Tukey’s multiple comparisons test: * P < 0.05 as compared with SOD1 WT ; ## P < 0.01 as compared with 150–400 μm 2 neurons

Journal: Acta Neuropathologica Communications

Article Title: Reduction of ephrin-A5 aggravates disease progression in amyotrophic lateral sclerosis

doi: 10.1186/s40478-019-0759-6

Figure Lengend Snippet: In the ventral horn of the spinal cord EfnA5 is mainly expressed in neurons. RNAscope in situ hybridization was performed to determine cell type-specific expression of EfnA5 . A total of 15–18 images of different lumbar spinal cord ventral horns from 3 different mice were analysed for every condition. a Representative images show lumbar spinal cord ventral horns of SOD1 WT and SOD1 G93A mice at 135 days of age that were stained with probes against EfnA5, Syp and Slc1a3 . Hoechst was used as a counter stain for nuclei. Scale bar = 50 μm. b Percentage of neurons ( Syp + cells) that stained positive for EfnA5 were quantified and shown as percentage of the total Syp + cells. c Glial cells ( Syp - cells) and d astrocytes ( Syp -, Slc1a3 + cells) positive for EfnA5 were quantified and represented as percentage of the total amount of glial cells. Single-cell EfnA5 expression was quantified by measuring EfnA5 puncta density (dots/μm 2 ) in e neurons, f glial cells and g astrocytes. Data represents mean ± SEM, and different conditions were compared with a two-tailed t-test: * P < 0.05; ** P < 0.01 as compared to SOD1 WT . b and e Data represents mean ± SEM, and different conditions were compared with a two-way ANOVA with Tukey’s multiple comparisons test: * P < 0.05 as compared with SOD1 WT ; ## P < 0.01 as compared with 150–400 μm 2 neurons

Article Snippet: For multiple reaction monitoring (MRM) analysis of efnA5 in CSF samples, 200 μL of CSF were spiked with TEAB buffer and a quantitative protein epitope signature tag (QPrEST, Atlas Antibodies AB, #QPrEST25042) of efnA5 as internal standard.

Techniques: RNAscope, In Situ Hybridization, Expressing, Staining, Two Tailed Test

Reduction of efnA5 levels in SOD1 G93A mice is detrimental and shortens survival and disease duration. Disease progression was closely monitored in a - f SOD1 G93A EfnA5 +/+ and SOD1 G93A EfnA5 +/− mice from the age of 60 days onwards ( N = 26–28). a Weight and b and c motor performance decline over time on b the hanging wire (HW) and c rotarod tests is shown. Data is represented as mean ± SEM and two-way ANOVA test with repeated measurements was used to determine differences among genotypes. d Disease onset differences were compared between the two genotypes with the Log-rank test whereas e survival was analysed with the two-tailed Mann-Whitney test for non-parametric data: * P < 0.05. f Disease duration was analysed with a two-tailed student t-test: * P < 0.05. g EfnA5 expression levels in the lumbar spinal cord of end-stage mice were determined by qPCR and data is represented as mean ± SEM ( N = 7–9). Different genotypes were compared with a one-way ANOVA with Tukey’s multiple comparisons test: *** P < 0.001

Journal: Acta Neuropathologica Communications

Article Title: Reduction of ephrin-A5 aggravates disease progression in amyotrophic lateral sclerosis

doi: 10.1186/s40478-019-0759-6

Figure Lengend Snippet: Reduction of efnA5 levels in SOD1 G93A mice is detrimental and shortens survival and disease duration. Disease progression was closely monitored in a - f SOD1 G93A EfnA5 +/+ and SOD1 G93A EfnA5 +/− mice from the age of 60 days onwards ( N = 26–28). a Weight and b and c motor performance decline over time on b the hanging wire (HW) and c rotarod tests is shown. Data is represented as mean ± SEM and two-way ANOVA test with repeated measurements was used to determine differences among genotypes. d Disease onset differences were compared between the two genotypes with the Log-rank test whereas e survival was analysed with the two-tailed Mann-Whitney test for non-parametric data: * P < 0.05. f Disease duration was analysed with a two-tailed student t-test: * P < 0.05. g EfnA5 expression levels in the lumbar spinal cord of end-stage mice were determined by qPCR and data is represented as mean ± SEM ( N = 7–9). Different genotypes were compared with a one-way ANOVA with Tukey’s multiple comparisons test: *** P < 0.001

Article Snippet: For multiple reaction monitoring (MRM) analysis of efnA5 in CSF samples, 200 μL of CSF were spiked with TEAB buffer and a quantitative protein epitope signature tag (QPrEST, Atlas Antibodies AB, #QPrEST25042) of efnA5 as internal standard.

Techniques: Biomarker Discovery, Two Tailed Test, MANN-WHITNEY, Expressing

Electromyography decline, neuronal loss and neuromuscular junction denervation in SOD1 G93A mice is not affected in SOD1 G93A mice with reduced efnA5 levels. a Compound muscle action potential amplitude (expressed in mV) was measured in SOD1 G93A EfnA5 +/+ and SOD1 G93A EfnA5 +/− mice from the age of 60 days (d) onwards. Data is represented as as mean ± SEM ( N = 7–8). b The number of motor neurons of different soma area was counted in the ventral horn of the lumbar spinal cord. Data is represented as mean ± SEM ( N = 6–7) and it was analysed with a two-way ANOVA. Representative image shows Neurotrace staining of a spinal cord slice. Scale bar = 50 μm. c and d Expression levels of c Rbfox3 and d Chat were unaltered after efnA5 knockdown in mice at 130 days of age. Data represents mean ± SEM ( N = 6–7), and different conditions were compared with a one-way ANOVA with Tukey’s multiple comparisons test: * P < 0.05; ** P < 0.01; *** P < 0.001 as compared with SOD1 WT mice. e Neuromuscular junctions (NMJs) innervation was scored in the gastrocnemius muscle. Data represents mean ± SEM ( N = 5–6) and it was analysed with a two-tailed t-test. Representative images are shown of denervated and innervated NMJs in the gastrocnemius muscle that were stained with neurofilament-L (NfL) and α-bungarotoxin (BTX). Scale bar = 50 μm

Journal: Acta Neuropathologica Communications

Article Title: Reduction of ephrin-A5 aggravates disease progression in amyotrophic lateral sclerosis

doi: 10.1186/s40478-019-0759-6

Figure Lengend Snippet: Electromyography decline, neuronal loss and neuromuscular junction denervation in SOD1 G93A mice is not affected in SOD1 G93A mice with reduced efnA5 levels. a Compound muscle action potential amplitude (expressed in mV) was measured in SOD1 G93A EfnA5 +/+ and SOD1 G93A EfnA5 +/− mice from the age of 60 days (d) onwards. Data is represented as as mean ± SEM ( N = 7–8). b The number of motor neurons of different soma area was counted in the ventral horn of the lumbar spinal cord. Data is represented as mean ± SEM ( N = 6–7) and it was analysed with a two-way ANOVA. Representative image shows Neurotrace staining of a spinal cord slice. Scale bar = 50 μm. c and d Expression levels of c Rbfox3 and d Chat were unaltered after efnA5 knockdown in mice at 130 days of age. Data represents mean ± SEM ( N = 6–7), and different conditions were compared with a one-way ANOVA with Tukey’s multiple comparisons test: * P < 0.05; ** P < 0.01; *** P < 0.001 as compared with SOD1 WT mice. e Neuromuscular junctions (NMJs) innervation was scored in the gastrocnemius muscle. Data represents mean ± SEM ( N = 5–6) and it was analysed with a two-tailed t-test. Representative images are shown of denervated and innervated NMJs in the gastrocnemius muscle that were stained with neurofilament-L (NfL) and α-bungarotoxin (BTX). Scale bar = 50 μm

Article Snippet: For multiple reaction monitoring (MRM) analysis of efnA5 in CSF samples, 200 μL of CSF were spiked with TEAB buffer and a quantitative protein epitope signature tag (QPrEST, Atlas Antibodies AB, #QPrEST25042) of efnA5 as internal standard.

Techniques: Staining, Expressing, Knockdown, Two Tailed Test

Reduction of efnA5 levels does not alter glial gene expression in symptomatic mice. Gene expression of several glial genes was quantified in the lumbar spinal cord of SOD1 WT , SOD1 G93A EfnA5 +/+ and SOD1 G93A EfnA5 +/− mice. a Aif , b Gfap , and c Vimentin levels were unaltered in SOD1 G93A EfnA5 +/− mice. Data represents mean ± SEM ( N = 6–7), and different conditions were compared with a one-way ANOVA with Tukey’s multiple comparisons test: * P < 0.05; ** P < 0.01; *** P < 0.001 as compared with SOD1 WT mice

Journal: Acta Neuropathologica Communications

Article Title: Reduction of ephrin-A5 aggravates disease progression in amyotrophic lateral sclerosis

doi: 10.1186/s40478-019-0759-6

Figure Lengend Snippet: Reduction of efnA5 levels does not alter glial gene expression in symptomatic mice. Gene expression of several glial genes was quantified in the lumbar spinal cord of SOD1 WT , SOD1 G93A EfnA5 +/+ and SOD1 G93A EfnA5 +/− mice. a Aif , b Gfap , and c Vimentin levels were unaltered in SOD1 G93A EfnA5 +/− mice. Data represents mean ± SEM ( N = 6–7), and different conditions were compared with a one-way ANOVA with Tukey’s multiple comparisons test: * P < 0.05; ** P < 0.01; *** P < 0.001 as compared with SOD1 WT mice

Article Snippet: For multiple reaction monitoring (MRM) analysis of efnA5 in CSF samples, 200 μL of CSF were spiked with TEAB buffer and a quantitative protein epitope signature tag (QPrEST, Atlas Antibodies AB, #QPrEST25042) of efnA5 as internal standard.

Techniques: Gene Expression

Whole proteome is not altered in the lumbar spinal cord of SOD1 G93A EfnA5 +/− compared to SOD1 G93A EfnA5 +/+ mice at 130 days of age. Differences at a proteomic level were determined for a SOD1 G93A EfnA5 +/+ versus SOD1 WT , and for b SOD1 G93A EfnA5 +/− versus SOD1 G93A EfnA5 +/+ mice. Data is represented in Volcano plots and the black lines indicate the significance level based on an FDR of 5% and S0 = 0.1 to correct for multiple testing

Journal: Acta Neuropathologica Communications

Article Title: Reduction of ephrin-A5 aggravates disease progression in amyotrophic lateral sclerosis

doi: 10.1186/s40478-019-0759-6

Figure Lengend Snippet: Whole proteome is not altered in the lumbar spinal cord of SOD1 G93A EfnA5 +/− compared to SOD1 G93A EfnA5 +/+ mice at 130 days of age. Differences at a proteomic level were determined for a SOD1 G93A EfnA5 +/+ versus SOD1 WT , and for b SOD1 G93A EfnA5 +/− versus SOD1 G93A EfnA5 +/+ mice. Data is represented in Volcano plots and the black lines indicate the significance level based on an FDR of 5% and S0 = 0.1 to correct for multiple testing

Article Snippet: For multiple reaction monitoring (MRM) analysis of efnA5 in CSF samples, 200 μL of CSF were spiked with TEAB buffer and a quantitative protein epitope signature tag (QPrEST, Atlas Antibodies AB, #QPrEST25042) of efnA5 as internal standard.

Techniques:

Axonal regeneration is not enhanced in EfnA5 knockout mice after sciatic nerve crush. Percentage of re-innervated neuromuscular junctions (NMJs) was determined in the a gastrocnemius and in the b tibialis anterior muscles in the ipsilateral and contralateral limbs of EfnA5 +/+ and EfnA5 −/− mice 11 days after the crush ( N = 5–5). Data represents mean ± SEM, and different conditions were compared with a two-tailed t-test. Representative images of ipsilateral and contralateral gastrocnemius and tibialis anterior muscles that were stained with neurofilament-L (NfL) and α-bungarotoxin (BTX) are shown. Scale bar = 50 μm

Journal: Acta Neuropathologica Communications

Article Title: Reduction of ephrin-A5 aggravates disease progression in amyotrophic lateral sclerosis

doi: 10.1186/s40478-019-0759-6

Figure Lengend Snippet: Axonal regeneration is not enhanced in EfnA5 knockout mice after sciatic nerve crush. Percentage of re-innervated neuromuscular junctions (NMJs) was determined in the a gastrocnemius and in the b tibialis anterior muscles in the ipsilateral and contralateral limbs of EfnA5 +/+ and EfnA5 −/− mice 11 days after the crush ( N = 5–5). Data represents mean ± SEM, and different conditions were compared with a two-tailed t-test. Representative images of ipsilateral and contralateral gastrocnemius and tibialis anterior muscles that were stained with neurofilament-L (NfL) and α-bungarotoxin (BTX) are shown. Scale bar = 50 μm

Article Snippet: For multiple reaction monitoring (MRM) analysis of efnA5 in CSF samples, 200 μL of CSF were spiked with TEAB buffer and a quantitative protein epitope signature tag (QPrEST, Atlas Antibodies AB, #QPrEST25042) of efnA5 as internal standard.

Techniques: Knock-Out, Muscles, Two Tailed Test, Staining

Disease progression is more severe in patients with lower CSF efnA5 protein levels. a Disease onset and b disease progression were determined in patients with CSF efnA5 levels above the median and in patients with CSF efnA5 levels below the median ( N = 32). Differences were compared between the two genotypes with the Log-rank test: ** p < 0.01

Journal: Acta Neuropathologica Communications

Article Title: Reduction of ephrin-A5 aggravates disease progression in amyotrophic lateral sclerosis

doi: 10.1186/s40478-019-0759-6

Figure Lengend Snippet: Disease progression is more severe in patients with lower CSF efnA5 protein levels. a Disease onset and b disease progression were determined in patients with CSF efnA5 levels above the median and in patients with CSF efnA5 levels below the median ( N = 32). Differences were compared between the two genotypes with the Log-rank test: ** p < 0.01

Article Snippet: For multiple reaction monitoring (MRM) analysis of efnA5 in CSF samples, 200 μL of CSF were spiked with TEAB buffer and a quantitative protein epitope signature tag (QPrEST, Atlas Antibodies AB, #QPrEST25042) of efnA5 as internal standard.

Techniques: Biomarker Discovery