Recombinant Human/Mouse/Rat GDF-8/Myostatin Protein

GMP Version Available: 788-GMP
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Carrier Free

Catalog # Availability Size / Price Qty
788-G8-010/CF
788-G8-100/CF
788-G8-250/CF

With Carrier

Catalog # Availability Size / Price Qty
788-G8-010
788-G8-100
788-G8-250
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Recombinant Human/Mouse/Rat GDF-8/Myostatin Protein Bioactivity
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Product Details
Citations (40)
FAQs
Reviews (3)

Recombinant Human/Mouse/Rat GDF-8/Myostatin Protein Summary

Product Specifications

Purity
>90%, by SDS-PAGE under reducing conditions and visualized by silver stain.
Endotoxin Level
<0.10 EU per 1 μg of the protein by the LAL method.
Activity
Measured by its ability to induce hemoglobin expression in K562 human chronic myelogenous leukemia cells. Schwall, R.H. et al. (1991) Method Enzymol. 198:340. The ED50 for this effect is 2-10 ng/mL.
Source
Mouse myeloma cell line, NS0-derived GDF-8/Myostatin protein
Asp268-Ser376
Accession #
N-terminal Sequence
Analysis
Asp268
Structure / Form
Disulfide-linked homodimer
Predicted Molecular Mass
12.4 kDa
SDS-PAGE
12 kDa, reducing conditions
24 kDa, non-reducing conditions

Product Datasheets

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788-G8 (with carrier)

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788-G8/CF (carrier free)

Carrier Free

What does CF mean?

CF stands for Carrier Free (CF). We typically add Bovine Serum Albumin (BSA) as a carrier protein to our recombinant proteins. Adding a carrier protein enhances protein stability, increases shelf-life, and allows the recombinant protein to be stored at a more dilute concentration. The carrier free version does not contain BSA.

What formulation is right for me?

In general, we advise purchasing the recombinant protein with BSA for use in cell or tissue culture, or as an ELISA standard. In contrast, the carrier free protein is recommended for applications, in which the presence of BSA could interfere.

788-G8

Formulation Lyophilized from a 0.2 μm filtered solution in Acetonitrile and TFA with BSA as a carrier protein. *1 mg pack size (01M) is supplied as a 0.2 µm filtered solution in Acetonitrile and TFA with BSA as a carrier protein.
Reconstitution Reconstitute at 100 μg/mL in sterile 4 mM HCl containing at least 0.1% human or bovine serum albumin.
Shipping The product is shipped at ambient temperature. Upon receipt, store it immediately at the temperature recommended below.
Stability & Storage: Use a manual defrost freezer and avoid repeated freeze-thaw cycles.
  • 12 months from date of receipt, -20 to -70 °C as supplied.
  • 1 month, 2 to 8 °C under sterile conditions after reconstitution.
  • 3 months, -20 to -70 °C under sterile conditions after reconstitution.

788-G8/CF

Formulation Lyophilized from a 0.2 μm filtered solution in Acetonitrile and TFA.
Reconstitution Reconstitute at 100 μg/mL in sterile 4 mM HCl.
Shipping The product is shipped at ambient temperature. Upon receipt, store it immediately at the temperature recommended below.
Stability & Storage: Use a manual defrost freezer and avoid repeated freeze-thaw cycles.
  • 12 months from date of receipt, -20 to -70 °C as supplied.
  • 1 month, 2 to 8 °C under sterile conditions after reconstitution.
  • 3 months, -20 to -70 °C under sterile conditions after reconstitution.

Scientific Data

Bioactivity Recombinant Human/Mouse/Rat GDF-8/Myostatin Protein Bioactivity View Larger

Recombinant Human/Mouse/Rat GDF-8/ Myostatin (Catalog # 788-G8) induces hemoglobin expression in the K562 human chronic myelogenous leukemia cell line. The ED50 for this effect is 2-10 ng/mL.

SDS-PAGE Recombinant Human/Mouse/Rat GDF-8/Myostatin Protein SDS-PAGE View Larger

1 μg/lane of Recombinant Human/Mouse/Rat GDF-8/Myostatin was resolved with SDS-PAGE under reducing (R) and non-reducing (NR) conditions and visualized by silver staining, showing the main bands at 12 kDa and 24 kDa, respectively.

Reconstitution Calculator

Reconstitution Calculator

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Background: GDF-8/Myostatin

Growth Differentiation Factor 8 (GDF-8), also known as myostatin, is a member of the TGF-beta superfamily that is expressed specifically in developing and adult skeletal muscle. GDF-8 cDNA encodes a 376 amino acid (aa) prepropeptide with a 24 aa residue signal peptide, a 223 aa residue amino-terminal propeptide, and a 109 aa residue carboxy-terminal mature protein. Mature GDF-8 contains the canonical 7-cysteine motif common to other TGF-beta superfamily members. Similar to the TGF‑ beta s, activins and BMP-11, GDF-8 also contains one extra pair of cysteine residues that is not found in other family members. The bioactive form of GDF-8 is a homodimer with an apparent molecular weight of approximately 25 kDa. GDF-8 is highly conserved across species. At the amino acid sequence level, mature human, mouse, rat and cow GDF-8 are 100% identical. Within the TGF-beta superfamily, GDF-8 is most closely related to BMP-11, a mammalian protein that acts as a dorsal mesoderm and neural inducer in Xenopus explants. The two proteins share 90% amino acid sequence identity within their mature chain. A targeted disruption of GDF-8 in mouse results in large mice with a widespread increase in skeletal muscle mass, indicating that GDF-8 is a negative regulator of skeletal muscle growth. A mutation in the bovine GDF-8 gene has been shown to be responsible for the double-muscled phenotype in cattle breeds such as Belgian Blue cattle that is characterized by an increase in muscle mass. GDF-8 has also been shown to inhibit preadipocyte differentiation to adipocytes. Mature GDF-8 binds to activin type II receptors and the binding is antagonized by the activin-binding protein, follistatin. R&D Systems recombinant GDF-8 preparations have been shown to act similarly to Activin A in both the Xenopus animal cap and the K562 assays.

References
  1. Storm, E.E. et al. (1994) Nature 368:639.
  2. Sharma, M. et al. (1999) J. Cell Physiol. 180:1.
  3. McPherron, A.C. et al. (1997) Nature 387:83.
  4. Lee, S.J. et al. (2001) Proc. Natl. Acad. Sci. USA 98:9306.
  5. Kim, H.S. et al. (2001) Biochem. Biophys. Res. Commun. 281:902.
Long Name
Growth Differentiation Factor 8
Entrez Gene IDs
2660 (Human); 17700 (Mouse)
Alternate Names
GDF8; GDF-8; GDF8growth differentiation factor 8; growth/differentiation factor 8; MSLHP; MSTN; Myostatin

Citations for Recombinant Human/Mouse/Rat GDF-8/Myostatin Protein

R&D Systems personnel manually curate a database that contains references using R&D Systems products. The data collected includes not only links to publications in PubMed, but also provides information about sample types, species, and experimental conditions.

40 Citations: Showing 1 - 10
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  1. Maternal immunization against myostatin suppresses post-hatch chicken growth
    Authors: R Mishra, R Jha, B Mishra, YS Kim
    PLoS ONE, 2022-10-06;17(10):e0275753.
    Species: Human
    Sample Types: Transfected Whole Cells
    Applications: Bioassay
  2. A New Method of Myostatin Inhibition in Mice via Oral Administration of Lactobacillus casei Expressing Modified Myostatin Protein, BLS-M22
    Authors: DK Sung, H Kim, SE Park, J Lee, JA Kim, YC Park, HB Jeon, JW Chang, J Lee
    International Journal of Molecular Sciences, 2022-08-13;23(16):.
    Species: Mouse
    Sample Types: Serum
    Applications: ELISA Capture
  3. TMEPAI/PMEPA1 Is a Positive Regulator of Skeletal Muscle Mass
    Authors: A Hagg, S Kharoud, G Goodchild, CA Goodman, JL Chen, RE Thomson, H Qian, P Gregorevic, CA Harrison, KL Walton
    Front Physiol, 2020-11-04;11(0):560225.
    Species: Human
    Sample Types: Whole Cells
    Applications: Bioassay
  4. The green tea polyphenol epigallocatechin-3-gallate attenuates age-associated muscle loss via regulation of miR-486-5p and myostatin
    Authors: YC Chang, HW Liu, YC Chan, SH Hu, MY Liu, SJ Chang
    Arch. Biochem. Biophys., 2020-07-22;692(0):108511.
    Species: Mouse
    Sample Types: Whole Cells
    Applications: Bioassay
  5. Myostatin Inhibits Vascular Smooth Muscle Cell Proliferation and Local 14q32 microRNA Expression, But Not Systemic Inflammation or Restenosis
    Authors: EAC Goossens, MR de Vries, JW Jukema, PHA Quax, AY Nossent
    Int J Mol Sci, 2020-05-15;21(10):.
    Species: Mouse
    Sample Types: In Vivo, Whole Cells
    Applications: Cell Culture, In Vivo
  6. Characterization of a novel compound that promotes myogenesis via�Akt and transcriptional co-activator with PDZ-binding motif (TAZ) in mouse C2C12 cells
    Authors: M Kodaka, F Mao, K Arimoto-Ma, M Kitamura, X Xu, Z Yang, K Nakagawa, J Maruyama, K Ishii, C Akazawa, T Oyaizu, N Yamamoto, M Ishigami-Y, N Tsuemoto, S Ito, H Kagechika, H Nishina, Y Hata
    PLoS ONE, 2020-04-08;15(4):e0231265.
    Species: Human
    Sample Types: Whole Cells
    Applications: Bioassay
  7. Structural basis of specific inhibition of extracellular activation of pro- or latent myostatin by the monoclonal antibody SRK-015
    Authors: KB Dagbay, E Treece, FC Streich, JW Jackson, RR Faucette, A Nikiforov, SC Lin, CJ Boston, SB Nicholls, AD Capili, GJ Carven
    J. Biol. Chem., 2020-02-19;295(16):5404-5418.
    Species: Human
    Sample Types: Cell Culture Supernates
  8. AdipoRon prevents myostatin-induced upregulation of fatty acid synthesis and downregulation of insulin activity in a mouse hepatocyte line
    Authors: XH Liu, JP Pan, WA Bauman, CP Cardozo
    Physiol Rep, 2019-08-01;7(13):e14152.
    Species: Mouse
    Sample Types: Whole Cells
    Applications: Bioassay, Cell Culture
  9. A GDF11/myostatin inhibitor, GDF11 propeptide-Fc, increases skeletal muscle mass and improves muscle strength in dystrophic mdx mice
    Authors: Q Jin, C Qiao, J Li, B Xiao, J Li, X Xiao
    Skelet Muscle, 2019-05-27;9(1):16.
    Species: Human
    Sample Types: Cell Lysates
    Applications: Bioassay
  10. Identification of the minimum region of flatfish myostatin propeptide (Pep45-65) for myostatin inhibition and its potential to enhance muscle growth and performance in animals
    Authors: JH Kim, JH Kim, LA Sutikno, SB Lee, DH Jin, YK Hong, YS Kim, HJ Jin
    PLoS ONE, 2019-04-18;14(4):e0215298.
    Species: Human
    Sample Types: Whole Cells
    Applications: Bioassay
  11. GDF8 enhances SOX2 expression and blastocyst total cell number in porcine IVF embryo development
    Authors: JD Yoon, SU Hwang, M Kim, G Lee, Y Jeon, SH Hyun
    Theriogenology, 2019-02-13;129(0):70-76.
    Species: Porcine
    Sample Types: Whole Tissue
    Applications: Bioassay
  12. Myostatin and activin blockade by engineered follistatin results in hypertrophy and improves dystrophic pathology in mdx mouse more than myostatin blockade alone
    Authors: A Iskenderia, N Liu, Q Deng, Y Huang, C Shen, K Palmieri, R Crooker, D Lundberg, N Kastrapeli, B Pescatore, A Romashko, J Dumas, R Comeau, A Norton, J Pan, H Rong, K Derakhchan, DE Ehmann
    Skelet Muscle, 2018-10-27;8(1):34.
    Species: Mouse
    Sample Types: Serum
  13. Biological scaffold-mediated delivery of myostatin inhibitor promotes a regenerative immune response in an animal model of Duchenne muscular dystrophy
    Authors: KM Estrellas, L Chung, LA Cheu, K Sadtler, S Majumdar, J Mula, MT Wolf, JH Elisseeff, KR Wagner
    J. Biol. Chem., 2018-08-23;0(0):.
    Species: Mouse
    Sample Types: In Vivo
    Applications: In Vivo
  14. JNK regulates muscle remodeling via myostatin/SMAD inhibition
    Authors: SJ Lessard, TL MacDonald, P Pathak, MS Han, VG Coffey, J Edge, DA Rivas, MF Hirshman, RJ Davis, LJ Goodyear
    Nat Commun, 2018-08-02;9(1):3030.
    Species: Mouse
    Sample Types: Whole Cells
    Applications: Bioassay
  15. Inhibition of the Activin Receptor Type-2B Pathway Restores Regenerative Capacity in Satellite Cell-Depleted Skeletal Muscle
    Authors: L Formicola, A Pannérec, RM Correra, B Gayraud-Mo, D Ollitrault, V Besson, S Tajbakhsh, J Lachey, JS Seehra, G Marazzi, DA Sassoon
    Front Physiol, 2018-05-24;9(0):515.
    Species: Mouse
    Sample Types: Whole Cells
    Applications: Bioassay
  16. Relative abundance of mature myostatin rather than total myostatin is negatively associated with bone mineral density in Chinese
    Authors: LF Wu, DC Zhu, BH Wang, YH Lu, P He, YH Zhang, HQ Gao, XW Zhu, W Xia, H Zhu, XB Mo, X Lu, L Zhang, YH Zhang, FY Deng, SF Lei
    J. Cell. Mol. Med., 2017-12-16;0(0):.
    Species: Human
    Sample Types: Whole Cells
    Applications: Bioassay
  17. The histone deacetylase SIRT6 blocks myostatin expression and development of muscle atrophy
    Authors: SA Samant, A Kanwal, VB Pillai, R Bao, MP Gupta
    Sci Rep, 2017-09-19;7(1):11877.
    Species: Mouse
    Sample Types: Whole Cells
    Applications: Bioassay
  18. Specific targeting of TGF-? family ligands demonstrates distinct roles in the regulation of muscle mass in health and disease
    Authors: JL Chen, KL Walton, A Hagg, TD Colgan, K Johnson, H Qian, P Gregorevic, CA Harrison
    Proc. Natl. Acad. Sci. U.S.A., 2017-06-12;0(0):.
    Species: Human
    Sample Types: Whole Cells
    Applications: Bioassay
  19. Activin A more prominently regulates muscle mass in primates than does GDF8
    Authors: E Latres, J Mastaitis, W Fury, L Miloscio, J Trejos, J Pangilinan, H Okamoto, K Cavino, E Na, A Papatheodo, T Willer, Y Bai, J Hae Kim, A Rafique, S Jaspers, T Stitt, AJ Murphy, GD Yancopoulo, J Gromada
    Nat Commun, 2017-04-28;8(0):15153.
    Species: Human
    Sample Types: Recombinant Protein
    Applications: Surface Plasmon Resonance
  20. A multiplexed immunocapture liquid chromatography tandem mass spectrometry assay for the simultaneous measurement of myostatin and GDF-11 in rat serum using an automated sample preparation platform
    Authors: Y Zhao, G Liu, FC Zambito, YJ Zhang, BS DeSilva, AT Kozhich, JX Shen
    Anal. Chim. Acta, 2017-04-26;979(0):36-44.
    Species: Rat
    Sample Types: Serum
    Applications: Bioassay
  21. Maltose binding protein-fusion enhances the bioactivity of truncated forms of pig myostatin propeptide produced in E. coli
    Authors: SB Lee, SK Park, YS Kim
    PLoS ONE, 2017-04-03;12(4):e0174956.
    Species: Human
    Sample Types: Whole Cells
    Applications: Bioassay
  22. Supraphysiological levels of GDF11 induce striated muscle atrophy
    Authors: DW Hammers, M Merscham-B, JY Hsiao, S Engst, JJ Hartman, HL Sweeney
    EMBO Mol Med, 2017-04-01;0(0):.
    Species: Human, Mouse
    Sample Types: Whole Cells
    Applications: Bioassay
  23. Structural basis for potency differences between GDF8 and GDF11
    Authors: RG Walker, M Czepnik, EJ Goebel, JC McCoy, A Vujic, M Cho, J Oh, S Aykul, KL Walton, G Schang, DJ Bernard, AP Hinck, CA Harrison, E Martinez-H, AJ Wagers, RT Lee, TB Thompson
    BMC Biol, 2017-03-03;15(1):19.
    Species: Human, Mouse
    Sample Types: In Vivo, Whole Cells
    Applications: Bioassay, In Vivo
  24. Myostatin propeptide mutation of the hypermuscular Compact mice decreases the formation of myostatin and improves insulin sensitivity
    Authors: Tamas Kocsis
    Am. J. Physiol. Endocrinol. Metab, 2016-12-13;0(0):ajpendo.00216.
    Applications: Control
  25. Myostatin blockade with a fully human monoclonal antibody induces muscle hypertrophy and reverses muscle atrophy in young and aged mice.
    Authors: Latres E, Pangilinan J, Miloscio L, Bauerlein R, Na E, Potocky T, Huang Y, Eckersdorff M, Rafique A, Mastaitis J, Lin C, Murphy A, Yancopoulos G, Gromada J, Stitt T
    Skelet Muscle, 2015-10-09;5(0):34.
    Species: Human
    Sample Types: Whole Cells
    Applications: Bioassay
  26. A Key Role for Leukemia Inhibitory Factor in C26 Cancer Cachexia.
    Authors: Seto D, Kandarian S, Jackman R
    J Biol Chem, 2015-06-19;290(32):19976-86.
    Species: Mouse
    Sample Types: Whole Cells
    Applications: Bioassay
  27. Small molecules dorsomorphin and LDN-193189 inhibit myostatin/GDF8 signaling and promote functional myoblast differentiation.
    Authors: Horbelt D, Boergermann J, Chaikuad A, Alfano I, Williams E, Lukonin I, Timmel T, Bullock A, Knaus P
    J Biol Chem, 2014-11-03;290(6):3390-404.
    Species: Human
    Sample Types: Whole Cells
    Applications: Bioassay
  28. Blockade of ActRIIB signaling triggers muscle fatigability and metabolic myopathy.
    Authors: Relizani K, Mouisel E, Giannesini B, Hourde C, Patel K, Morales Gonzalez S, Julich K, Vignaud A, Pietri-Rouxel F, Fortin D, Garcia L, Blot S, Ritvos O, Bendahan D, Ferry A, Ventura-Clapier R, Schuelke M, Amthor H
    Mol Ther, 2014-05-27;22(8):1423-33.
    Species: Mouse
    Sample Types: Whole Cells
    Applications: Bioassay
  29. Myostatin regulates energy homeostasis in the heart and prevents heart failure.
    Authors: Biesemann N, Mendler L, Wietelmann A, Hermann S, Schafers M, Kruger M, Boettger T, Borchardt T, Braun T
    Circ Res, 2014-05-07;115(2):296-310.
    Species: Mouse
    Sample Types: Whole Cells
    Applications: Bioassay
  30. Screening with a novel cell-based assay for TAZ activators identifies a compound that enhances myogenesis in C2C12 cells and facilitates muscle repair in a muscle injury model.
    Authors: Yang, Zeyu, Nakagawa, Kentaro, Sarkar, Aradhan, Maruyama, Junichi, Iwasa, Hiroaki, Bao, Yijun, Ishigami-Yuasa, Mari, Ito, Shigeru, Kagechika, Hiroyuki, Hata, Shoji, Nishina, Hiroshi, Abe, Shinya, Kitagawa, Masanobu, Hata, Yutaka
    Mol Cell Biol, 2014-02-18;34(9):1607-21.
    Species: Mouse
    Sample Types: Whole Cells
    Applications: Bioassay
  31. Myostatin stimulates, not inihibits, C2C12 myoblast proliferation.
    Authors: Rodgers B, Wiedeback B, Hoversten K, Jackson M, Walker R, Thompson T
    Endocrinology, 2014-01-01;155(3):670-5.
    Species: Mouse
    Sample Types: Whole Cells
    Applications: Bioassay
  32. Self-renewal of embryonic-stem-cell-derived progenitors by organ-matched mesenchyme.
    Authors: Sneddon, Julie B, Borowiak, Malgorza, Melton, Douglas
    Nature, 2012-10-07;491(7426):765-8.
    Species: Human
    Sample Types: Whole Cells
    Applications: Cell Culture
  33. Widespread potential for growth-factor-driven resistance to anticancer kinase inhibitors.
    Authors: Wilson TR, Fridlyand J, Yan Y, Penuel E, Burton L, Chan E, Peng J, Lin E, Wang Y, Sosman J, Ribas A, Li J, Moffat J, Sutherlin DP, Koeppen H, Merchant M, Neve R, Settleman J
    Nature, 2012-07-26;487(7408):505-9.
    Species: Human
    Sample Types: Whole Cells
    Applications: Bioassay
  34. Analysis of the effects of androgens and training on myostatin propeptide and follistatin concentrations in blood and skeletal muscle using highly sensitive Immuno PCR.
    Authors: Diel P, Schiffer T, Geisler S, Hertrampf T, Mosler S, Schulz S, Wintgens KF, Adler M
    Mol. Cell. Endocrinol., 2010-08-27;330(1):1-9.
    Applications: ELISA (Standard)
  35. Loss-of-function mutation in myostatin reduces tumor necrosis factor alpha production and protects liver against obesity-induced insulin resistance.
    Authors: Wilkes JJ, Lloyd DJ, Gekakis N
    Diabetes, 2009-02-10;58(5):1133-43.
    Species: Mouse
    Sample Types: In Vivo
    Applications: In Vivo
  36. A new model for growth factor activation: type II receptors compete with the prodomain for BMP-7.
    Authors: Sengle G, Ono RN, Lyons KM, Bachinger HP, Sakai LY
    J. Mol. Biol., 2008-07-02;381(4):1025-39.
    Species: Human
    Sample Types: Recombinant Protein
    Applications: ELISA Developmet, Surface Plasmon Resonance
  37. Targeting of bone morphogenetic protein growth factor complexes to fibrillin.
    Authors: Sengle G, Charbonneau NL, Ono RN, Sasaki T, Alvarez J, Keene DR, Bachinger HP, Sakai LY
    J. Biol. Chem., 2008-03-13;283(20):13874-88.
    Species: Human
    Sample Types: Recombinant Protein
    Applications: Binding Assay, Surface Plasmon Resonance
  38. Gene transfer demonstrates that muscle is not a primary target for non-cell-autonomous toxicity in familial amyotrophic lateral sclerosis.
    Authors: Miller TM, Kim SH, Yamanaka K, Hester M, Umapathi P, Arnson H, Rizo L, Mendell JR, Gage FH, Cleveland DW, Kaspar BK
    Proc. Natl. Acad. Sci. U.S.A., 2006-12-12;103(51):19546-51.
    Species: Mouse
    Sample Types: Whole Cells
    Applications: Bioassay
  39. Muscular atrophy of caveolin-3-deficient mice is rescued by myostatin inhibition.
    Authors: Ohsawa Y, Hagiwara H, Nakatani M, Yasue A, Moriyama K, Murakami T, Tsuchida K, Noji S, Sunada Y
    J. Clin. Invest., 2006-10-12;116(11):2924-34.
    Species: Human
    Sample Types: Whole Cells
    Applications: Bioassay
  40. Follistatin complexes Myostatin and antagonises Myostatin-mediated inhibition of myogenesis.
    Authors: Amthor H, Nicholas G, McKinnell I, Kemp CF, Sharma M, Kambadur R, Patel K
    Dev. Biol., 2004-06-01;270(1):19-30.
    Species: Chicken
    Sample Types: Whole Tissue
    Applications: Bioassay

FAQs

  1. Is Recombinant Human/Mouse/Rat GDF-8/Myostatin Protein (Catalog # 788-G8) the mature form of GDF8?

    • The mature form of GDF8 consists of a disulfide-linked homodimer. Catalog 788-G8 consists of Asp268-Ser376. There are multiple disulfide bonds within this sequence, which form a disulfide-linked heterodimer with another Asp268-Ser376 molecule.

View all Proteins and Enzyme FAQs

Reviews for Recombinant Human/Mouse/Rat GDF-8/Myostatin Protein

Average Rating: 4.3 (Based on 3 Reviews)

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Recombinant Human/Mouse/Rat GDF-8/Myostatin Protein
By Sampath Kumar Anandan on 04/15/2024
Application: Immunoassay Standard
Reason for Rating: I had used the recombinant GDF-8/Myostatin as a positive control for my immunoblotting experiments. The recombinant GDF-8/myostatin at 1μg concentration produced a strong signal just above 20kDa.

Upon receipt of the recombinant myostatin, i reconstituted it in 4 mM HCl.

I had loaded 1μg of recombinant myostatin/GDF8 into a Bio-Rad PROTEAN TGX 4-15% gel, performed electrophoresis with NuPAGE MES buffer and blotted the gel onto 0.2μm nitrocellulose membrane.

For the immuno-detection, I had used the R&D systems goat polyclonal GDF8 antibody (BAF788) at 0.1 or 0.25 µg/mL concentration, and the R&D system anti-goat secondary antibody (HAF017) at 1:4000 dilution.


Recombinant Human/Mouse/Rat GDF-8/Myostatin Protein
By Anonymous on 04/07/2020
Application: In vitro bioactivity in cell culture

Recombinant Human/Mouse/Rat GDF-8/Myostatin Protein
By Shelley Anderson on 10/20/2017
Application: Immunoassay Standard