Myostatin ELISA
$751.00
Catalog
30-1012
The Myostatin ELISA is for the quantitative determination of Myostatin in plasma and serum samples. Research Use Only. Not for Use in Diagnostic Procedures.
Species
Human
Regulatory Status
Research Use Only. Not for Use in Diagnostic Procedures.
Product Distribution
Available in North America Only
Range
12 - 325 ng/mL
Sensitivity
12 ng/mL
Sizes
96 Wells
Sample Types
Plasma, Serum
Inc Time Hour
5
Inc Time Overnight
No
Inc Time See Protocol
No
Sample Size
30
Detection
Colorimetric
Myostatin belongs to the transforming growth differentiation factor-ß (TGF-ß)
super family. The molecule is a negative regulator of muscle growth, but details about the actions of myostatin are uncertain (Roth and Walsh, 2004). Myostatin was first identified in 1997 by McPherron et al. They found out that null-mutant knockout mice were significantly larger than wild-type animals and exhibited a large and widespread increase in skeletal muscle mass due to an increase of muscle fiber number (hyperplasia) and thickness (hypertrophy).
Other groups identified mutations in the myostatin gene in naturally bred “double-muscles†cattle breeds. Similar to the findings in animal models, increased myostatin immunoreactivity or expression has been observed in HIV-infected men with muscle wasting (Gonzales-Cadavid et al. 1998), after prolonged bed rest in young
men (Zachwieja et al. 1999) and in older men and women with muscle wasting (Yarasheski KE et al. 2002). Shi et al. (2007) and others have found that myostatin deficiency inhibits adipogenesis in vivo, even when mice are fed a high-fat diet. Transgenic overexpression of myostatin pro-peptide, which inhibits myostatin signaling, also inhibits body fat gain with a high-fat diet (Zhao et al. 2005).
super family. The molecule is a negative regulator of muscle growth, but details about the actions of myostatin are uncertain (Roth and Walsh, 2004). Myostatin was first identified in 1997 by McPherron et al. They found out that null-mutant knockout mice were significantly larger than wild-type animals and exhibited a large and widespread increase in skeletal muscle mass due to an increase of muscle fiber number (hyperplasia) and thickness (hypertrophy).
Other groups identified mutations in the myostatin gene in naturally bred “double-muscles†cattle breeds. Similar to the findings in animal models, increased myostatin immunoreactivity or expression has been observed in HIV-infected men with muscle wasting (Gonzales-Cadavid et al. 1998), after prolonged bed rest in young
men (Zachwieja et al. 1999) and in older men and women with muscle wasting (Yarasheski KE et al. 2002). Shi et al. (2007) and others have found that myostatin deficiency inhibits adipogenesis in vivo, even when mice are fed a high-fat diet. Transgenic overexpression of myostatin pro-peptide, which inhibits myostatin signaling, also inhibits body fat gain with a high-fat diet (Zhao et al. 2005).
