Recombinant Human Sonic Hedgehog/Shh Protein, High Activity
Recombinant Human Sonic Hedgehog/Shh Protein, High Activity Summary
Product Specifications
Cys24-Gly197
Analysis
Product Datasheets
Carrier Free
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.
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.
8908-SH
Formulation | Supplied as a 0.2 μm filtered solution in MES, NaCl and CHAPS with BSA as a carrier protein. |
Shipping | The product is shipped with dry ice or equivalent. Upon receipt, store it immediately at the temperature recommended below. |
Stability & Storage: | Use a manual defrost freezer and avoid repeated freeze-thaw cycles.
|
8908-SH/CF
Formulation | Supplied as a 0.2 μm filtered solution in MES, NaCl and CHAPS. |
Shipping | The product is shipped with dry ice or equivalent. Upon receipt, store it immediately at the temperature recommended below. |
Stability & Storage: | Use a manual defrost freezer and avoid repeated freeze-thaw cycles.
|
Scientific Data
Recombinant Human Shh proteins induce alkaline phosphatase production by mesenchymal stem cells. High Activity Shh (green), purified from HEK293 cells and containing the correct post-translational modifications (cholesterol and fatty acids), is over 14-fold more active than E. coli-purified Recombinant Human Shh-N (C24II) N-Terminus (Catalog # 1845-SH; red line), and over 250-fold more active than E. coli-purified Recombinant Human Shh-N (Catalog # 1314-SH; blue line).
1 μg/lane of Recombinant Human Sonic Hedgehog/Shh Protein was resolved with SDS-PAGE under reducing (R) and non-reducing (NR) conditions and visualized by silver staining, showing 18-24 kDa bands.
LC/ESI-MS analysis of Recombinant Human (rh)SHH Protein, High Activity shows major peaks at 20119.3, 20145.2, and 20171.6 Da, suggesting that recombinant human SHH molecules are dual-modified with cholesterol at C-terminus, and fatty acids (lauric acid, myristic acid, and palmitic acid) at the N-terminus. The minor peaks at 19776 Da corresponds to rhSHH with only fatty acid modification.
Reconstitution Calculator
Background: Sonic Hedgehog/Shh
The Sonic Hedgehog (Shh) protein is expressed in embryonic tissues that are critical for the patterning of the developing central nervous system, somite, and limb. It is also involved in whisker, hair, foregut, tooth, and bone development. The Shh protein regulates neural and hematopoietic stem cell fate and is important for thymocyte differentiation and proliferation as well as T cell determination. In adult tissue, Shh is associated with cancer development and tissue remodeling following injury (1-3). Human Shh encodes a 462 amino acid (aa) precursor Shh protein that is autocatalytically processed to yield a non-glycosylated 19 kDa N-terminal fragment (Shh-N) and a glycosylated 25 kDa C-terminal protein (Shh-C) (4). The Shh-C protein, which is responsible for the intramolecular processing of Shh, is rapidly degraded following Shh proteolysis (5). The Shh-N protein is highly conserved, sharing >98% aa identity between mouse, human, rat, canine, porcine, and chicken Shh-N. Shh-N can be palmitoylated at its N-terminal cysteine and modified by cholesterol addition at its C-terminus (6). These modifications contribute to the membrane tethering of the Shh protein as well as its assembly into various sized multimers (6-9). Lipid modification and multimerization greatly increase the receptor binding affinity and signaling potency of the Shh-N protein (5, 6, 8, 9). Monomeric and multimeric Shh can be released from the plasma membrane by the cooperative action of DISP1, SCUBE2, and TACE/ADAM17 (10-12). Modifications also extend the effective range of functionality of the Shh protein and are required for the development of Shh protein gradients important in tissue morphogenesis (9, 13). Canonical signaling by the Shh protein is mediated by a multicomponent receptor complex that includes Patched (PTCH1, PTCH2) and Smoothened (SMO) (14). Binding of the Shh protein to PTCH releases the basal repression of SMO by PTCH. Shh activity can also be regulated through interactions with heparin, glypicans, and membrane-associated Hip (hedgehog interacting protein) (13, 15, 16).
- Briscoe, J. and P.P. Therond (2013) Mol. Cell. Biol. 14:416.
- Aviles, E.C. et al. (2013) Front. Cell. Neurosci. 7:86.
- Xie, J. et al. (2013) OncoTargets Ther. 6:1425.
- Marigo, V. et al. (1995) Genomics 28:44.
- Zeng, X. et al. (2001) Nature 411:716.
- Feng, J. et al. (2004) Development 131:4357.
- Goetz, J.A. et al. (2006) J. Biol. Chem. 281:4087.
- Pepinsky, R.B. et al. (1998) J. Biol. Chem. 273:14037.
- Chen, M.-H. et al. (2004) Genes Dev. 18:641.
- Etheridge, L.A. et al. (2010) Development 137:133.
- Jakobs, P. et al. (2014) J. Cell Sci. 127:1726.
- Dierker, T. et al. (2009) J. Biol. Chem. 284:8013.
- Lewis, P.M. et al. (2001) Cell 105:599.
- Carpenter, D. et al. (1998) Proc. Natl. Acad. Sci. USA 95:13630.
- Filmus, J. and M. Capurro (2014) Matrix Biol. 35:248.
- Chuang, P.-T. and A.P. McMahon (1999) Nature 397:617.
Citations for Recombinant Human Sonic Hedgehog/Shh Protein, High Activity
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.
12
Citations: Showing 1 - 10
Filter your results:
Filter by:
-
Two-way Dispatched function in Sonic hedgehog shedding and transfer to high-density lipoproteins
Authors: Ehring, K;Ehlers, SF;Froese, J;Gude, F;Puschmann, J;Grobe, K;
eLife
Species: Mouse
Sample Types: Transfected Whole Cells
Applications: Bioassay -
Diffusion barriers imposed by tissue topology shape Hedgehog morphogen gradients
Authors: Schlissel, G;Meziane, M;Narducci, D;Hansen, AS;Li, P;
Proceedings of the National Academy of Sciences of the United States of America
Species: Mouse
Sample Types: Whole Cells
Applications: Bioassay -
Increasing Ciliary ARL13B Expression Drives Active and Inhibitor-Resistant Smoothened and GLI into Glioma Primary Cilia
Authors: Shi, P;Tian, J;Mallinger, JC;Ling, D;Deleyrolle, LP;McIntyre, JC;Caspary, T;Breunig, JJ;Sarkisian, MR;
Cells
Species: Human
Sample Types: Whole Cells
Applications: Bioassay -
Structural insights into proteolytic activation of the human Dispatched1 transporter for Hedgehog morphogen release
Authors: W Li, L Wang, BM Wierbowski, M Lu, F Dong, W Liu, S Li, P Wang, A Salic, X Gong
Nature Communications, 2021-11-29;12(1):6966.
Species: Human
Sample Types: Recombinant Protein
Applications: Bioassay -
Forebrain Shh overexpression improves cognitive function and locomotor hyperactivity in an aneuploid mouse model of Down syndrome and its euploid littermates
Authors: FJ Gao, D Klinedinst, FX Fernandez, B Cheng, A Savonenko, B Devenney, Y Li, D Wu, MG Pomper, RH Reeves
Acta neuropathologica communications, 2021-08-16;9(1):137.
Species: Transgenic Mouse
Sample Types: Whole Cells
Applications: Bioassay -
SLITRK5 is a negative regulator of hedgehog signaling in osteoblasts
Authors: J Sun, DY Shin, M Eiseman, AR Yallowitz, N Li, S Lalani, Z Li, M Cung, S Bok, S Debnath, SJ Marquez, TE White, AG Khan, IC Lorenz, JH Shim, FS Lee, R Xu, MB Greenblatt
Nature Communications, 2021-07-29;12(1):4611.
Species: Human
Sample Types: Whole Cells
Applications: Bioassay -
PAUPAR and PAX6 sequentially regulate human embryonic stem cell cortical differentiation
Authors: Y Xu, J Xi, G Wang, Z Guo, Q Sun, C Lu, L Ma, Y Wu, W Jia, S Zhu, X Guo, S Bian, J Kang
Nucleic Acids Research, 2021-02-26;0(0):.
Species: Human
Sample Types: Whole Cells
Applications: Bioassay -
GLI2 but not GLI1/GLI3 plays a central role in the induction of malignant phenotype of gallbladder cancer
Authors: S Ichimiya, H Onishi, S Nagao, S Koga, K Sakihama, K Nakayama, A Fujimura, Y Oyama, A Imaizumi, Y Oda, M Nakamura
Oncology reports, 2021-01-22;45(3):997-1010.
Species: Human
Sample Types: Whole Cells
Applications: Bioassay -
Nicotinamide restricts neural precursor proliferation to enhance catecholaminergic neuronal subtype differentiation from mouse embryonic stem cells
Authors: SM Griffin, MR Pickard, CP Hawkins, AC Williams, RA Fricker
PLoS ONE, 2020-09-14;15(9):e0233477.
Species: Mouse
Sample Types: Whole Cells
Applications: Bioassay -
Defects in mRNA Translation in LRRK2-Mutant hiPSC-Derived Dopaminergic Neurons Lead to Dysregulated Calcium Homeostasis
Authors: JW Kim, X Yin, A Jhaldiyal, MR Khan, I Martin, Z Xie, T Perez-Rose, M Kumar, L Abalde-Atr, J Xu, L Chen, SM Eacker, DJ Surmeier, NT Ingolia, TM Dawson, VL Dawson
Cell Stem Cell, 2020-08-25;27(4):633-645.e7.
Species: Human
Sample Types: Whole Cells
Applications: Bioassay -
Structures of human Patched and its complex with native palmitoylated sonic hedgehog
Authors: X Qi, P Schmiege, E Coutavas, J Wang, X Li
Nature, 2018-07-11;0(0):.
Species: Human
Sample Types: Recombinant Protein
Applications: Bioassay -
Roles of Ihh signaling in chondroprogenitor function in postnatal condylar cartilage
Authors: N Kurio, C Saunders, TE Bechtold, I Salhab, HD Nah, S Sinha, PC Billings, M Pacifici, E Koyama
Matrix Biol., 2018-02-12;0(0):.
Species: Mouse
Sample Types: Whole Cells
Applications: Bioassay
FAQs
No product specific FAQs exist for this product, however you may
View all Proteins and Enzyme FAQsReviews for Recombinant Human Sonic Hedgehog/Shh Protein, High Activity
Average Rating: 4 (Based on 1 Review)
Have you used Recombinant Human Sonic Hedgehog/Shh Protein, High Activity?
Submit a review and receive an Amazon gift card.
$25/€18/£15/$25CAN/¥75 Yuan/¥2500 Yen for a review with an image
$10/€7/£6/$10 CAD/¥70 Yuan/¥1110 Yen for a review without an image
Filter by:
Reason for Rating: n/a