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The protein encoded by MSTN is a member of the bone morphogenetic protein (BMP) family and the TGF-beta superfamily. Additionally we are shipping Myostatin Antibodies (204) and Myostatin Proteins (73) and many more products for this protein.
Showing 10 out of 60 products:
Human MSTN ELISA Kit for Sandwich ELISA - ABIN366562
Astorino, Harness, Witzke: Chronic activity-based therapy does not improve body composition, insulin-like growth factor-I, adiponectin, or myostatin in persons with spinal cord injury. in The journal of spinal cord medicine 2014
Show all 2 references for ABIN366562
Mouse (Murine) MSTN ELISA Kit for Sandwich ELISA - ABIN845470
Takada, Miwa, Sato: Expression of myostatin in early postnatal mouse masseter and rectus femoris muscles. in Histology and histopathology 2015
Show all 2 references for ABIN845470
improving muscle growth in a fish species by mixing a classical strategy, such as compensatory growth, and a biotechnological approach, such as the use of recombinant proteins for inhibiting the biological actions of MSTN(Myostatin)
the expression of myostatin during development and the effects of its knock-down on various genes such as muscle regulatory transcription factors (MRFs), muscle-specific (show EIF3K ELISA Kits) proteins (MSP (show MST1 ELISA Kits)), and insulin (show INS ELISA Kits)-like growth factors (IGFs).
Epistatic analyses suggest a possible genetic interaction between Wnt (show WNT2 ELISA Kits)/beta-catenin (show CTNNB1 ELISA Kits) and Myostatin in regulation of slow and fast twitch muscle myofibrillogenesis
Findings suggest that myostatin (MSTN) function is required for regulating the appropriate growth of skeletal muscle in medaka
Myostatin is a well-described negative regulator of postnatal skeletal and cardiac muscle mass and modulates metabolic processes. It functions in the heart, skeletal muscle, and brain. Review.
Plasma myostatin levels are increased in chronic obstructive pulmonary disease patients who have cor pulmonale.
In human granulosa cells, GDF8 may play an important role in the modulation of cellular responsiveness to gonadotropins and in the regulation of ovarian steroid production, most likely as a luteinization inhibitor.
Plasma myostatin might be suitable in predicting weight regain after marked weight loss, but no association with weight loss was observed in patients undergoing a non-surgical weight loss program.
Plasma MSTN level was elevated in an early stage of CKD, which could be involved in the progression of sarcopenia.
it is becoming clearer that besides its conventional role in muscle, myostatin plays a critical role in metabolism. Hence, molecular mechanisms by which myostatin regulates several key metabolic processes need to be further explored.
The aim of this study was to investigate MSTN polymorphisms in an elderly sarcopenic population in Turkey and determine how they relate to sarcopenia.
There is a significant decrease in levels of circulating myostatin in postsurgical acute phase reaction.
Myostatin myocardial expression increases in the presence of structural cardiomyopathy either of hypertensive or other origin.
In contrast to elite endurance and power track and field athletes, the MSTN 153RR genotype was not found in short distance-swimmers, and among the long distance-swimmers it was not associated with top level swimming performance.
Agouti-related peptide (AgRP (show AGRP ELISA Kits)) neuron activation acutely reprograms gene expression in BAT (show BAAT ELISA Kits) toward a myogenic signature, including increased expression of myostatin. Interference with myostatin activity improves insulin (show INS ELISA Kits) sensitivity that was impaired by AgRP (show AGRP ELISA Kits) neurons activation.
Increased expression of myostatin in heart muscle cells caused interstitial fibrosis via activation of the TAK-1 (show NR2C2 ELISA Kits)-MKK3 (show MAP2K3 ELISA Kits)/6-p38 (show CRK ELISA Kits) signaling pathway
study is the first to report an in vivo association between vitamin D, myostatin, and the regulation of muscle mass
Report myostatin expression in early postnatal mouse masseter and rectus femoris muscles.
An age-dependent decline in serum Gdf8 levels was identified.
Mstn may negatively regulate Igf2 expression to control postnatal skeletal muscle growth, however differences in growth between male and female mice are not readily explained by changes in expression of Igf family members.
the phenotypic and physiologic impact of postnatal myostatin inhibition on bite mechanics, were examined.
Data (including data from studies in knockout mice) suggest that myostatin attenuation stimulates adipogenesis in vivo; reduced adiposity in mstn-/- knockout mice results from nutrient partitioning away from fat and in support of muscle.
analysis of dual exon skipping of dystrophin (show DMD ELISA Kits) and myostatin pre-mRNAs using phosphorodiamidate morpholino oligomers conjugated with an arginine-rich peptide
Data show that circulating myostatin levels decreased with age and estimates of growth differentiation factor 11 (GDF11 (show GDF11 ELISA Kits)) levels using myostatin null mice indicate that they were almost 500 times lower than those for myostatin.
Single nucleotide polymorphisms in the MYOD1 (show MYOD1 ELISA Kits) and GDF8 genes are associated with genetic transcription during myogenesis in pigs.
The level of myostatin inversely correlated with miR (show MYLIP ELISA Kits)-27a in fat and heart of pigs and also in proliferating porcine myoblasts. Overexpression of miR (show MYLIP ELISA Kits)-27a in porcine myoblasts promoted cell proliferation by reducing the expression of myostatin.
MSTN g.435G>A and g.447A>G affected carcass traits in pigs
The genotypes of MSTN g.435G > A and g.447A > G SNPs in Duroc pigs were studied. The 435GG/447AA (show COL16A1 ELISA Kits) individually had significantly higher average daily gain, body weight at 70 d and 150 d , and a lower age at 110 kg than 435AA/447GG individuals.
Porcine MSTN could be upregulated by isobutyl-1-methylxanthine , MyoD (show MYOD1 ELISA Kits), and PPARgamma (show PPARG ELISA Kits) but downregulated by C/EBPalpha (show CEBPA ELISA Kits) and C/EBPbeta (show CEBPB ELISA Kits).
a vital enhancer region was identified between nucleotides -218 and -137 in promoter region of porcine myostatin
It was concluded that myostatin is a factor broadly expressed in the internal organs and muscle tissues of pigs.
In this study, haplotypes involving 3 polymorphic sites in the promoter region of the porcine myostatin gene were identified and their effect on production traits, gene expression as well as on skeletal muscle traits were analysed.
In both skeletal muscle and heart muscle growth, the insulin-like growth factor-2 (show IGF2 ELISA Kits):myostatin interaction seems to play an important role.
A comparative analysis of the pig BAC sequence involved in the regulation of MSTN was performed.
Data indicate that the the promoter trap vector PIII-myostatin could knock out the bovine myostatin gene.
The effects of myostatin and myogenic factor 5 (show MYF5 ELISA Kits) polymorphisms on growth and muscle traits of Marchigiana breed were assessed.
we demonstrate zygote injection of TALEN mRNA can also produce gene-edited cattle and sheep. In both species we have targeted the myostatin (MSTN) gene.
proof-of-concept study is the first to produce MSTN mutations in cattle, and may allow the development of genetically modified strains of double-muscled cattle.
Mutations in the leader peptide of the bovine myostatin gene effectively promote the proliferation of bovine fibroblast cells.
there were 18 SNPs identified in the Qinchuan cattle promoter region compared with those of other cattle compared to the Red Angus cattle myostatin promoter region.
A 3-way interaction of myostatin genotype (MG), season, and trigonometric function periodicities of 24 h and 12 h indicate that a genotype x environment interaction exists for MG.
These results show for the first time that myostatin regulates the differential expression of chemokines in skeletal muscle cells.
bovine myostatin is a specific target of miR (show MYLIP ELISA Kits)-27b and that miRNAs contribute to explain additive phenotypic hypertrophy in Piedmontese cattle selected for the MSTN gene mutation
Mutations in the myostatin gene, responsible for the double muscling condition in cattle, were targeted to estimate the time since the most recent common ancestor. Each myostatin allele had a recent common ancestor (<400 years ago).
The reduced expression of myostatin gene was achieved and measured in clonal fibroblast cells by real-time PCR.
This study also suggests the importance of siRNA-mediated knockdown of MSTN as a potential alternative to increase muscle mass and meat production.
A study of the MSTN 5' upstream region and investigation of 5'UTR (show UTS2R ELISA Kits) TTTTA deletion was carried out in seven different Indian goat breeds. An 1181 bp fragment of 5' upstream region of MSTN gene was PCR amplified, cloned, and sequenced.
myostatin plays a negative role in regulating the expression of adipogenesis related genes in goat fetal fibroblasts.
Polymorphisms of myostatin gene as markers associated with growth in Boer goats.
The effect of an Equine Repetitive Element 1 insertion in the promoter of the myostatin gene, which is involved in muscle development, was also investigated.
Myostatin mRNA but not protein was increased in skeletal muscle of obese compared with lean animals. Myostatin mRNA was increased in crest fat of obese animals and protein was undetectable. Serum myostatin was higher in obese than lean animals.
The tissue-specific presence of myostatin, the moystatin receptor (activin receptor IIB (show ACVR2B ELISA Kits), ActRIIB (show ACVR2B ELISA Kits)), follistatin (show FST ELISA Kits) and perilipin (show PLIN1 ELISA Kits), genes and proteins across a range of equine tissues, were examined.
The candidate for racing performance genomic region contained eight genes annotated by ENSEMBL, including the myostatin gene (MSTN).
Polymorphisms of the MSTN promoter region in 5 horse breeds in Poland are reported.
significant association observed between genotype and mRNA abundance for untrained horses with the C/C cohort having highest MSTN mRNA levels,T/T group lowest levels and C/T group intermediate levels; following training there was significant decrease in MSTN mRNA which was most apparent for the C/C cohort
Exon 2 of the MSTN gene, which encodes part of the TGF-beta (show TGFB1 ELISA Kits) pro-peptide, was sequenced in 332 horses of 20 different breeds and compared with the horse MSTN gene sequence deposited in GenBank. The sequences obtained revealed the presence of 11 haplotypes represented by 10 variable nucleotide mutations, eight of them corresponding to amino acid sequence changes.
Variation at the MSTN gene influences speed in Thoroughbred horses.
This study demonstrates that the g.66493737C>T single nucleotide polymorphism in MSTN provides the most powerful genetic marker for prediction of race distance aptitude in Thoroughbreds.
Characterized the horse (Equus caballus) MSTN gene and identified and analysed single nucleotide polymorphisms (SNPs) in breeds of different morphological types.
Alignment of sequence data with the GenBank sequence of the rabbit MSTN gene identified three single nucleotide polymorphisms (SNPs). Significant linkage was found between the novel SNP c.373+234G>A and nine carcass composition traits.
These results suggest that the mutations in the upstream regulatory region of the MSTN gene are beneficial to the rabbit soma development, and the mutations can be used as molecular markers for the selection of the meat quality of rabbits.
Studied and compared mRNA levels of myostatin (MSTN), myogenin (MyoG (show MYOG ELISA Kits)), and myosin heavy chain (MyHC) in skeletal muscles of two rabbit breeds with different body sizes and growth rates.
indicated that MSTN is not an important source of variability for performance traits, at least in the rabbit population
The protein encoded by this gene is a member of the bone morphogenetic protein (BMP) family and the TGF-beta superfamily. This group of proteins is characterized by a polybasic proteolytic processing site which is cleaved to produce a mature protein containing seven conserved cysteine residues. The members of this family are regulators of cell growth and differentiation in both embryonic and adult tissues. This gene is thought to encode a secreted protein which negatively regulates skeletal muscle growth.
Growth/differentiation factor 8
, growth/differentiation factor-8
, growth differentiation factor 8
, growth/differentiation factor 8