Recombinant human Activin A protein (Qk001)2020-03-31T12:45:40+00:00

Recombinant human Activin A protein (Qk001)

Activin A (ActA) is a member of the TGFβ superfamily of growth factors involved in stem cell differentiation and maintenance, regulation of embryogenesis, development of the reproductive system, wound healing and regulation of immune responses. The activity of Activin A is regulated by the high-affinity inhibitor, follistatin (1), and inhibins.
Activins are disulfide-linked homo- and heterodimers of four inhibin β chains. The best characterized are Activin A and Activin B, homodimers of inhibin βA and inhibin βB respectively. Activins, like all other members in the TGF-β superfamily, are synthesized as larger precursors consisting of an N-terminal signal peptide, a pro-domain of 250–350 residues and a highly conserved mature domain. The pro-domain, which is cleaved off in the mature protein, has important roles in the biosynthesis, stabilization, transportation and signalling of the growth factors (2).
Recombinant human Activin A protein is used for maintenance of pluripotency in many human induced-pluripotent stem cell and human embryonic stem cell lines (3), and to induce stem cell differentiation into endoderm (4) and other cell fates.

Qk001 Activin A protein has been extensively validated and benchmarked with other suppliers in stem cell culture and other assays. View the results of this analysis and a commentary by Qkine’s founder Marko Hyvonen.

Summary: Qk001 mature domain of human activin A (residues 311-426, Uniprot: P08476) expressed in E. coli. The mature protein is a disulfide-linked dimer.

Molecular mass: ~26 kDa (for the dimer)

Form: protein is provided lyophilized from a fully volatile solution.  Carrier protein-free.

  • Qk001: Activin A (human)

    Recombinant mature domain of human Activin A protein (residues 311-426, Uniprot: P08476) expressed in E.coli (animal-derived component free).  Protein supplied lyophilized with no carrier protein present. Activin A is used in stem cell maintenance and differentiation.
Activin A is very poorly soluble in physiological solutions. Please follow the handling guidance for lyophilized cytokines below to minimize loss of protein due to precipitation or adsorption to plastic.  We advise storing the recombinant protein at very low pH to before dilution in cell culture media or final working solutions. Low pH will also assist in maintaining the correct disulphide structure of the protein by minimizing disulphide bond exchange reactions.

  • Resuspension in physiological buffers may cause precipitation of stock solutions, hence we recommend dissolving our lyophilized cytokines in 10 mM HCl (1:1000 dilution of concentrated HCl) while keeping the protein concentration at 50 µg/ml or above, in order to avoid loss by adsorption to plasticware.
  • To ensure you recover all of the protein, let the sample sit for a few minutes with the solubilization buffer at room temperature and pipette gently up and down (avoid foaming).
  • Rinse the tube with some more 10 mM HCl and pool with the rest.
  • The protein is tolerant of some freeze and thaw cycles, but as always with proteins, it is better to aliquot and stored frozen.
  • Our protein are supplied carrier-protein free.  If compatible with your work, add carrier protein of your choice such as BSA, HSA or gelatin to further minimize loss by adsorption.
  • Store in -80°C for long term storage. -20°C for short-term.

ActA, Activin beta-A chain, Erythroid differentiation protein (EDP), Follicle-Stimulating Hormone (FSH) releasing protein (FRP), INHBA, Inhibin beta A, Inhibin beta 1

1. Harrington, A. E. et al. Structural basis for the inhibition of activin signalling by follistatin. EMBO J. 25, 1035–1045 (2006).
2. Wang, X., Fischer, G. & Hyvönen, M. Structure and activation of pro-activin A. (2016). doi:10.1038/ncomms12052
3. Pauklin, S. & Vallier, L. Activin/Nodal signalling in stem cells. Development 142, 607–19 (2015).
4. D’Amour, K. A. et al. Efficient differentiation of human embryonic stem cells to definitive endoderm. Nat. Biotechnol. 23, 1534–1541 (2005).

Result: ActA migrates as a single band at 24 kDa in non-reducing (NR) and 13 kDa as a single monomeric species upon reduction (R).  No contaminating protein bands are visible.

Activin A runs as 26kDa dimer in non-reduced conditions

Purified recombinant protein (7 µg) was resolved using 15% w/v SDS-PAGE in reduced (+β-mercaptothanol, R) and non-reduced conditions (NR) and stained with Coomassie Brilliant Blue R250.  Data from Qk001 batch #011

Result: ActA activity is determined using an activin responsive firefly luciferase reporter in HEK293T cells.  EC50 = 6.1 pM .  EC50 is within the expected range of 6 ± 2 pM.

Bioactivity is determined using an activin responsive firefly luciferase reporter in HEK293T cells.  Cells are treated (in triplicate) with a serial dilution of activin A for 6 hours.  Firefly luciferase activity is measured and normalized to the control Renilla luciferase activity. Data from Qk001 batch #011

Result: calculated molecular mass of the Activin A dimer is 25932 Da. Result of the analysis: 25934 Da which is consistent with the calculated mass.  No significant heterogeneity is present.

MALDI mass spectrometric analysis is used to confirm the molecular mass of the intact protein and to reveal any heterogeneity that would not be evident in SDS-PAGE analysis. The results are compared with calculated mass of the protein with the assumption that all the cysteines are disulphide-linked. The different peaks represent different charge states of the protein.  Data from Qk001 batch #011

Result: Reverse phase chromatogram shows single sharp peak showing that the protein is pure and homogeneous.

Protein purity and structural homogeneity is analyzed by reversed phase chromatography. 50 µg of protein, at 0.1 mg/ml in 10 mM HCl is analyzed in ACE C4 4.6 x 250 mm column using eluted using a 10 – 90 % acetonitrile gradient in 0.1 % trifluoroacetic acid . Homogeneity is judged by the absence of multiple peaks and by the symmetry of the main peak. Blue line shows absorbance at 280 nm and the green line the acetonitrile gradient.  Example data from Qk001 batch #011

Result: UV spectrum shows full recovery of protein following aliquoting and lyophilization.

Absorbance at 280 nm: average 0.158
Recovered concentration: 0.158 cm-1 x 10 / 1.446 cm-1 mg ml-1 = 1.09 mg / ml
Recovery: 110% (>100% due to routine 10% over-fill of vials during aliquoting)

The sample was reconstituted in 10 mM HCl to a theoretical concentration of 1 mg/ml following instructions above. This was diluted 1:10 in 6 M guanidine hydrochloride, 20 mM sodium phosphate pH 7.4 and the UV spectrum 340-220 nm. Concentration was calculated using extinction coefficient at 280 nm.  Example data from Qk001 batch #011

Result: Endotoxin level <0.005 EU/ug protein (below level of detection)

Stem cell cultures are sensitive to endotoxins1, which can be present in media, serum and as a contaminant on plasticware.  We optimize our protein production processes to ensure the lowest possible levels of endotoxin contamination.    Our endotoxin pass criteria are set at the industry leading <0.1 EU per ug protein and we aim for <0.01 EU per ug protein.  Endotoxin levels in our proteins are determined by an external expert microbiological testing services provider.  Example data from Qk001 batch #011

1. A biological study establishing the endotoxin limit for in vitro proliferation of human mesenchymal stem cells (2017). Yusuke Nomura, Chie Fukui, Yuki Morishita, Yuji Haishima. Regenerative Therapy, 7, 45-51.

View full batch quality testing data for Qk001

Batch #010, #011

All our proteins are produced in our Cambridge, UK, labs.  We provide detailed quality data for each batch because we believe reliable, high quality cytokines and growth factors are critical for successful stem cell and organoid culture.

When we test our proteins, we choose a vial at random and reconstitute as recommended to ensure we are testing as close to the protein you will receive as possible.  Biochemical identity and purity is checked using SDS-PAGE, mass spectrometry and analytical reverse phase chromatography.  Bioactivity is determined using an appropriate cell-based assay.  As stem cells are sensitive to endotoxin levels, we use a high resolution test to ensure endotoxin levels are at industry leading low levels (<0.01 EU per µg protein).  We also check that the correct amount of protein is recovered from the vial – it might sound basic but if you order 100 µg, we believe you should receive 100 µg so when you use the proteins you can rely on your calculated dilution.

Please contact us with questions any time by email or phone +44 (0) 1223 491486 / US toll free 1-866 877 2185.

Order online and upload your PO or pay by credit card, whichever is easiest for you, or email your PO to

We also provide bulk orders and stock reservation for sensitive applications, please email us.

  • Qk001: Activin A (human)

    Recombinant mature domain of human Activin A protein (residues 311-426, Uniprot: P08476) expressed in E.coli (animal-derived component free).  Protein supplied lyophilized with no carrier protein present. Activin A is used in stem cell maintenance and differentiation.

Our products are for research use only and not for diagnostic or therapeutic use.  Products are not for resale.