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GDF-8 Protein, Human/Mouse/Rat

GDF-8 Protein, Human/Mouse/Rat

Catalog Number: UA040576 Brand: UA BIOSCIENCE
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Regular price $310 USD
Regular price Sale price $310 USD
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Product Details

Product Specification


Species Human
Synonyms Growth/differentiation factor 8, GDF-8, Myostatin
Accession O14793
Amino Acid Sequence

Asp267-Ser375

Expression System CHO
Molecular Weight

12-13 kDa (Reducing)

Purity >95% by SDS-PAGE & HPLC.
Endotoxin <0.1EU/μg
Conjugation Unconjugated
Tag No Tag
Physical Appearance Lyophilized powder
Storage Buffer

4 mM HCl

Reconstitution

Reconstitute at 0.1-1 mg/ml according to the size in Reconstitution Buffer after rapid centrifugation.

Stability & Storage

·12 months from date of receipt, lyophilized powder stored at -20 to -80℃.
·3 months, -20 to -80℃ under sterile conditions after reconstitution.
·1 week, 2 to 8℃ under sterile conditions after reconstitution.
·Please avoid repeated freeze-thaw cycles.

Reference

Nature. 1997;387(6628):83-90.
Nat Genet. 1997;17(1):71-74.

Background

Growth differentiation factor-8 (GDF-8), commonly known as myostatin, is a ~25 kDa secreted glycoprotein belonging to the transforming growth factor-β (TGF-β) superfamily. GDF-8 is synthesized as a 376-amino acid prepropeptide, proteolytically processed to generate a latent prodomain-mature domain complex; activation requires further cleavage by tolloid-like proteases to release the biologically active mature dimer. The mature GDF-8 signals primarily through the activin type II receptor (ActRIIB), recruiting ALK4/ALK5 to activate Smad2/3 transcription factors, thereby suppressing myoblast proliferation, satellite cell activation, and muscle protein synthesis.

In 2004, a landmark case report described a human child with a homozygous myostatin mutation exhibiting gross muscle hypertrophy from infancy, providing direct proof-of-concept for therapeutic targeting in humans. Beyond muscle, GDF-8 influences adipogenesis (promoting fat accumulation), bone remodeling, cardiac hypertrophy, and tendon homeostasis.

Picture

Bioactivity

Determined by its ability to inhibit the proliferation of MPC-11 cells. The expected IC50 for this effect is 40-53 ng/ml.

SDS-PAGE

2μg (R: reducing condition, N: non-reducing condition).

RP-HPLC

>95% as determined by RP-HPLC.