capturing antibody for myom3 Search Results


myomesin  (Developmental Studies Hybridoma Bank)
95
Developmental Studies Hybridoma Bank myomesin
Myomesin, supplied by Developmental Studies Hybridoma Bank, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 95 stars, based on 1 article reviews
myomesin - by Bioz Stars, 2026-03
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polyclonal anti myom3 antibody  (Proteintech)
94
Proteintech polyclonal anti myom3 antibody
Early death associated with severe muscle atrophy in dystrophin-deficient R-DMDdup10-17 (DMD) rats. (A) Scheme of CRISPR/Cas9-mediated duplication on the rat chromosome X of a ~ 125 kb genomic region encompassing exons 10 to 17 of the Dmd gene. The wild-type allele (X + ) is at the top, with the reading frame indicated by the blue colour of the exons. The allele containing the duplication (X DMD ) is at the bottom. Splicing between exon 17 and the duplicated exon 10 induces a premature stop codon in the duplicated exon 10 (white cross on red background) and the absence of translation of subsequent exons (grey). The position and orientation of the primers used for genotyping is indicated by arrows, as is the expected amplicon size for each of the two alleles. (B) Electrophoretic gel of amplicons obtained using a multiplex of the three primers indicated in (A) from genomic DNA of male rats from a litter born from a carrier female and a WT male. A band at 130 bp reveals the WT allele, while a band at 277 bp reveals a male hemizygous for the Dmd allele carrying the duplicated 10–17 region. (C) Body mass of WT and DMD littermates at 6 and 10 months of age. (D) Kaplan-Meier curve for the frequency of WT (black curve) and DMD (orange curve) rat survival. (E) Representative immunofluorescence for laminin (red) and dystrophin (orange) at 6 months on TA, diaphragm and heart sections of WT and DMD littermates, showing complete absence of a dystrophin signal in DMD muscles. Scale bars, 50 μm. (F) Plasma CK levels in 7-month-old WT and DMD littermates. One-tailed unpaired t test. (G) Upper panel: Capillary immunoelectrophoresis plasma protein analysis detecting the two fragments (100 and 130 kDa) of the sarcomeric myomesin-3 <t>(MYOM3)</t> protein in 7-month-old DMD rats, but not in their WT littermates; lower panel: total proteins for each lane. (H) Quantification of plasma MYOM3 levels assessed in ( G ), corresponding to the sum of both MYOM3-130 and MYOM3-100 signals normalised to total plasma proteins. One-tailed unpaired t test. (I) Plasma hs-cTNT levels in 10-month-old WT and DMD littermates. One-tailed unpaired t test
Polyclonal Anti Myom3 Antibody, supplied by Proteintech, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/polyclonal anti myom3 antibody/product/Proteintech
Average 94 stars, based on 1 article reviews
polyclonal anti myom3 antibody - by Bioz Stars, 2026-03
94/100 stars
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myom3 plasma concentration  (Proteintech)
94
Proteintech myom3 plasma concentration
Early death associated with severe muscle atrophy in dystrophin-deficient R-DMDdup10-17 (DMD) rats. (A) Scheme of CRISPR/Cas9-mediated duplication on the rat chromosome X of a ~ 125 kb genomic region encompassing exons 10 to 17 of the Dmd gene. The wild-type allele (X + ) is at the top, with the reading frame indicated by the blue colour of the exons. The allele containing the duplication (X DMD ) is at the bottom. Splicing between exon 17 and the duplicated exon 10 induces a premature stop codon in the duplicated exon 10 (white cross on red background) and the absence of translation of subsequent exons (grey). The position and orientation of the primers used for genotyping is indicated by arrows, as is the expected amplicon size for each of the two alleles. (B) Electrophoretic gel of amplicons obtained using a multiplex of the three primers indicated in (A) from genomic DNA of male rats from a litter born from a carrier female and a WT male. A band at 130 bp reveals the WT allele, while a band at 277 bp reveals a male hemizygous for the Dmd allele carrying the duplicated 10–17 region. (C) Body mass of WT and DMD littermates at 6 and 10 months of age. (D) Kaplan-Meier curve for the frequency of WT (black curve) and DMD (orange curve) rat survival. (E) Representative immunofluorescence for laminin (red) and dystrophin (orange) at 6 months on TA, diaphragm and heart sections of WT and DMD littermates, showing complete absence of a dystrophin signal in DMD muscles. Scale bars, 50 μm. (F) Plasma CK levels in 7-month-old WT and DMD littermates. One-tailed unpaired t test. (G) Upper panel: Capillary immunoelectrophoresis plasma protein analysis detecting the two fragments (100 and 130 kDa) of the sarcomeric myomesin-3 <t>(MYOM3)</t> protein in 7-month-old DMD rats, but not in their WT littermates; lower panel: total proteins for each lane. (H) Quantification of plasma MYOM3 levels assessed in ( G ), corresponding to the sum of both MYOM3-130 and MYOM3-100 signals normalised to total plasma proteins. One-tailed unpaired t test. (I) Plasma hs-cTNT levels in 10-month-old WT and DMD littermates. One-tailed unpaired t test
Myom3 Plasma Concentration, supplied by Proteintech, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/myom3 plasma concentration/product/Proteintech
Average 94 stars, based on 1 article reviews
myom3 plasma concentration - by Bioz Stars, 2026-03
94/100 stars
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primary antibody myom3 17692-1-ap  (Proteintech)
90
Proteintech primary antibody myom3 17692-1-ap
Early death associated with severe muscle atrophy in dystrophin-deficient R-DMDdup10-17 (DMD) rats. (A) Scheme of CRISPR/Cas9-mediated duplication on the rat chromosome X of a ~ 125 kb genomic region encompassing exons 10 to 17 of the Dmd gene. The wild-type allele (X + ) is at the top, with the reading frame indicated by the blue colour of the exons. The allele containing the duplication (X DMD ) is at the bottom. Splicing between exon 17 and the duplicated exon 10 induces a premature stop codon in the duplicated exon 10 (white cross on red background) and the absence of translation of subsequent exons (grey). The position and orientation of the primers used for genotyping is indicated by arrows, as is the expected amplicon size for each of the two alleles. (B) Electrophoretic gel of amplicons obtained using a multiplex of the three primers indicated in (A) from genomic DNA of male rats from a litter born from a carrier female and a WT male. A band at 130 bp reveals the WT allele, while a band at 277 bp reveals a male hemizygous for the Dmd allele carrying the duplicated 10–17 region. (C) Body mass of WT and DMD littermates at 6 and 10 months of age. (D) Kaplan-Meier curve for the frequency of WT (black curve) and DMD (orange curve) rat survival. (E) Representative immunofluorescence for laminin (red) and dystrophin (orange) at 6 months on TA, diaphragm and heart sections of WT and DMD littermates, showing complete absence of a dystrophin signal in DMD muscles. Scale bars, 50 μm. (F) Plasma CK levels in 7-month-old WT and DMD littermates. One-tailed unpaired t test. (G) Upper panel: Capillary immunoelectrophoresis plasma protein analysis detecting the two fragments (100 and 130 kDa) of the sarcomeric myomesin-3 <t>(MYOM3)</t> protein in 7-month-old DMD rats, but not in their WT littermates; lower panel: total proteins for each lane. (H) Quantification of plasma MYOM3 levels assessed in ( G ), corresponding to the sum of both MYOM3-130 and MYOM3-100 signals normalised to total plasma proteins. One-tailed unpaired t test. (I) Plasma hs-cTNT levels in 10-month-old WT and DMD littermates. One-tailed unpaired t test
Primary Antibody Myom3 17692 1 Ap, supplied by Proteintech, 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/result/primary antibody myom3 17692-1-ap/product/Proteintech
Average 90 stars, based on 1 article reviews
primary antibody myom3 17692-1-ap - by Bioz Stars, 2026-03
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anti-myomesin 3 antibodies  (Kaneka Corp)
90
Kaneka Corp anti-myomesin 3 antibodies
Early death associated with severe muscle atrophy in dystrophin-deficient R-DMDdup10-17 (DMD) rats. (A) Scheme of CRISPR/Cas9-mediated duplication on the rat chromosome X of a ~ 125 kb genomic region encompassing exons 10 to 17 of the Dmd gene. The wild-type allele (X + ) is at the top, with the reading frame indicated by the blue colour of the exons. The allele containing the duplication (X DMD ) is at the bottom. Splicing between exon 17 and the duplicated exon 10 induces a premature stop codon in the duplicated exon 10 (white cross on red background) and the absence of translation of subsequent exons (grey). The position and orientation of the primers used for genotyping is indicated by arrows, as is the expected amplicon size for each of the two alleles. (B) Electrophoretic gel of amplicons obtained using a multiplex of the three primers indicated in (A) from genomic DNA of male rats from a litter born from a carrier female and a WT male. A band at 130 bp reveals the WT allele, while a band at 277 bp reveals a male hemizygous for the Dmd allele carrying the duplicated 10–17 region. (C) Body mass of WT and DMD littermates at 6 and 10 months of age. (D) Kaplan-Meier curve for the frequency of WT (black curve) and DMD (orange curve) rat survival. (E) Representative immunofluorescence for laminin (red) and dystrophin (orange) at 6 months on TA, diaphragm and heart sections of WT and DMD littermates, showing complete absence of a dystrophin signal in DMD muscles. Scale bars, 50 μm. (F) Plasma CK levels in 7-month-old WT and DMD littermates. One-tailed unpaired t test. (G) Upper panel: Capillary immunoelectrophoresis plasma protein analysis detecting the two fragments (100 and 130 kDa) of the sarcomeric myomesin-3 <t>(MYOM3)</t> protein in 7-month-old DMD rats, but not in their WT littermates; lower panel: total proteins for each lane. (H) Quantification of plasma MYOM3 levels assessed in ( G ), corresponding to the sum of both MYOM3-130 and MYOM3-100 signals normalised to total plasma proteins. One-tailed unpaired t test. (I) Plasma hs-cTNT levels in 10-month-old WT and DMD littermates. One-tailed unpaired t test
Anti Myomesin 3 Antibodies, supplied by Kaneka Corp, 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/result/anti-myomesin 3 antibodies/product/Kaneka Corp
Average 90 stars, based on 1 article reviews
anti-myomesin 3 antibodies - by Bioz Stars, 2026-03
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myom3 antibody  (Biosynth Carbosynth)
N/A
MYOM3 antibody was raised in Rabbit using Human MYOM3 as the immunogen. Rabbit polyclonal MYOM3 antibody.
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myom3 antibody c terminal region arp70910 p050  (Aviva Systems)
N/A
This is a rabbit polyclonal antibody against MYOM3 It was validated on Western Blot by Aviva Systems Biology At Aviva Systems Biology we manufacture rabbit polyclonal antibodies on a large scale 200 1000 products month
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anti myom3 aa 328 420 polyclonal antibody  (Creative BioMart)
N/A
This gene encodes a member of the bicoid sub family of homeodomain containing transcription factors The encoded protein acts as a transcription factor and may play a role in brain and sensory organ development Two
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myom3 antibody  (Abbexa)
N/A
MYOM3 Antibody is a Rabbit Polyclonal against MYOM3
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myom3 polyclonal antibody  (Thermo Fisher)
N/A
MYOM3 Polyclonal Antibody for IHC
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myom3 antibody  (biorbyt)
N/A
Rabbit polyclonal antibody to Myoferlin Isotype Note IgG Host Note Rabbit Conjugation Note Unconjugated Reactivity Note Human Mouse Rat Application Note WB IHC P P ELISA
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anti myom3 aa 430 512 polyclonal antibody  (Creative BioMart)
N/A
Olfactory receptors interact with odorant molecules in the nose to initiate a neuronal response that triggers the perception of a smell The olfactory receptor proteins are members of a large family of G protein coupled
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Image Search Results


Early death associated with severe muscle atrophy in dystrophin-deficient R-DMDdup10-17 (DMD) rats. (A) Scheme of CRISPR/Cas9-mediated duplication on the rat chromosome X of a ~ 125 kb genomic region encompassing exons 10 to 17 of the Dmd gene. The wild-type allele (X + ) is at the top, with the reading frame indicated by the blue colour of the exons. The allele containing the duplication (X DMD ) is at the bottom. Splicing between exon 17 and the duplicated exon 10 induces a premature stop codon in the duplicated exon 10 (white cross on red background) and the absence of translation of subsequent exons (grey). The position and orientation of the primers used for genotyping is indicated by arrows, as is the expected amplicon size for each of the two alleles. (B) Electrophoretic gel of amplicons obtained using a multiplex of the three primers indicated in (A) from genomic DNA of male rats from a litter born from a carrier female and a WT male. A band at 130 bp reveals the WT allele, while a band at 277 bp reveals a male hemizygous for the Dmd allele carrying the duplicated 10–17 region. (C) Body mass of WT and DMD littermates at 6 and 10 months of age. (D) Kaplan-Meier curve for the frequency of WT (black curve) and DMD (orange curve) rat survival. (E) Representative immunofluorescence for laminin (red) and dystrophin (orange) at 6 months on TA, diaphragm and heart sections of WT and DMD littermates, showing complete absence of a dystrophin signal in DMD muscles. Scale bars, 50 μm. (F) Plasma CK levels in 7-month-old WT and DMD littermates. One-tailed unpaired t test. (G) Upper panel: Capillary immunoelectrophoresis plasma protein analysis detecting the two fragments (100 and 130 kDa) of the sarcomeric myomesin-3 (MYOM3) protein in 7-month-old DMD rats, but not in their WT littermates; lower panel: total proteins for each lane. (H) Quantification of plasma MYOM3 levels assessed in ( G ), corresponding to the sum of both MYOM3-130 and MYOM3-100 signals normalised to total plasma proteins. One-tailed unpaired t test. (I) Plasma hs-cTNT levels in 10-month-old WT and DMD littermates. One-tailed unpaired t test

Journal: Skeletal Muscle

Article Title: Extensive striated muscle damage in a rat model of Duchenne muscular dystrophy with Dmd exons 10–17 duplication

doi: 10.1186/s13395-025-00386-2

Figure Lengend Snippet: Early death associated with severe muscle atrophy in dystrophin-deficient R-DMDdup10-17 (DMD) rats. (A) Scheme of CRISPR/Cas9-mediated duplication on the rat chromosome X of a ~ 125 kb genomic region encompassing exons 10 to 17 of the Dmd gene. The wild-type allele (X + ) is at the top, with the reading frame indicated by the blue colour of the exons. The allele containing the duplication (X DMD ) is at the bottom. Splicing between exon 17 and the duplicated exon 10 induces a premature stop codon in the duplicated exon 10 (white cross on red background) and the absence of translation of subsequent exons (grey). The position and orientation of the primers used for genotyping is indicated by arrows, as is the expected amplicon size for each of the two alleles. (B) Electrophoretic gel of amplicons obtained using a multiplex of the three primers indicated in (A) from genomic DNA of male rats from a litter born from a carrier female and a WT male. A band at 130 bp reveals the WT allele, while a band at 277 bp reveals a male hemizygous for the Dmd allele carrying the duplicated 10–17 region. (C) Body mass of WT and DMD littermates at 6 and 10 months of age. (D) Kaplan-Meier curve for the frequency of WT (black curve) and DMD (orange curve) rat survival. (E) Representative immunofluorescence for laminin (red) and dystrophin (orange) at 6 months on TA, diaphragm and heart sections of WT and DMD littermates, showing complete absence of a dystrophin signal in DMD muscles. Scale bars, 50 μm. (F) Plasma CK levels in 7-month-old WT and DMD littermates. One-tailed unpaired t test. (G) Upper panel: Capillary immunoelectrophoresis plasma protein analysis detecting the two fragments (100 and 130 kDa) of the sarcomeric myomesin-3 (MYOM3) protein in 7-month-old DMD rats, but not in their WT littermates; lower panel: total proteins for each lane. (H) Quantification of plasma MYOM3 levels assessed in ( G ), corresponding to the sum of both MYOM3-130 and MYOM3-100 signals normalised to total plasma proteins. One-tailed unpaired t test. (I) Plasma hs-cTNT levels in 10-month-old WT and DMD littermates. One-tailed unpaired t test

Article Snippet: MYOM3 plasma concentration was obtained with the SimpleProtein Jess analyzer (BioTechne) using the regular 12–230 kDa kit, the polyclonal anti-MYOM3 antibody (ProteinTech #17692-1-AP, 1:2000) and the anti-rabbit HRP (ProteinSimple).

Techniques: CRISPR, Amplification, Multiplex Assay, Immunofluorescence, Muscles, Clinical Proteomics, One-tailed Test, Immunoelectrophoresis