Recombinant Human/Mouse Indian Hedgehog/Ihh (C28II) N-Term Summary
Product Specifications
Cys28-Gly202 (Cys28Ile-Ile), with an N-terminal Met
Analysis
Product Datasheets
1705-HH/CF (carrier free)
Discontinued Product
1705-HH
| Formulation | Lyophilized from a 0.2 μm filtered solution in NaH2PO4, NaCl and DTT with Trehalose and with BSA as a carrier protein. |
| Reconstitution | Reconstitute at 200 μg/mL in sterile water 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.
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Reconstitution Calculator
Background: Indian Hedgehog/Ihh
The hedgehog (hh) gene encoding a secreted protein was originally identified in Drosophila as a segment polarity gene. The vertebrate homologues of Hh comprise several proteins including sonic hedgehog (Shh), Indian hedgehog (Ihh), and Desert hedgehog (Dhh) (1). Hedgehog proteins are important signaling molecules during embryonic development and are highly conserved within and across species (1). Mouse and human Ihh share 100% amino acid identity in the signaling domain, while mouse Ihh and Shh share 90% amino acid identity in the N-terminal signaling domain. Ihh mRNA expression is detected in fetal lung, gut, stomach, liver, kidney, pancreas and strongly in cartilage - in growth regions of the developing bone (2, 3). Ihh, along with parathyroid hormone related protein, regulate the rate of chondrocyte proliferation and differentiation (4). Ihh is also involved in yolk sac vasculogenesis, playing an important role in differentiation of epiblast cells into endothelial and red blood cells (5).
Mouse Ihh cDNA encodes a 411 amino acid (aa) polypeptide with a predicted 27 aa signal peptide. This polypeptide is cleaved to generate a 45 kDa precursor protein that undergoes the same post‑translation processing as Shh (3). An autocatalytic reaction yields a 19 kDa amino‑terminal domain Ihh‑N protein that retains all known signaling capabilities, and a 23 kDa carboxy‑terminal domain Ihh-C protein (3). Since hydrophobic modifications to Shh, including the substitution of the N-terminal cysteine residue with two hydrophobic isoleucine residues, can also increase its potency (6), a similar modification was made for Ihh. This modified form also shows increased potency in a bioassay measuring induction of alkaline phosphatase. At the cell surface, Hedgehog activity is mediated by a multicomponent receptor complex involving the 12‑pass transmembrane protein Patched (Ptc) which binds Hedgehogs with high affinity and Smoothened (Smo), a signaling seven transmembrane G-protein coupled receptor (1).
- Ingham, P. and A. McMahon (2001) Genes & Dev. 15:3059.
- Marigo, V. et al. (1995) Genomics 28:44.
- Valentini, R.P. et al. (1997) J Biol Chem. 272:8466.
- Vortkamp, A. et al. (1996) Science 273:613.
- Byrd, N. et al. (2002) Development 129:361.
- Taylor, F.R. et al. (2001) Biochemistry 40:4359.
Citations for Recombinant Human/Mouse Indian Hedgehog/Ihh (C28II) N-Term
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.
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Citations: Showing 1 - 8
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Altered IHH signaling contributes to reduced chondrocyte proliferation in the growth plate of MPS VII mice
Authors: Z Jiang, ALK Derrick-Ro, S Byers
Mol Genet Metab Rep, 2020-10-22;25(0):100668.
Species: Mouse
Sample Types: Whole Cells
Applications: Bioassay -
Regulation of Calvarial Osteogenesis by Concomitant De-repression of GLI3 and Activation of IHH Targets
Authors: LK Veistinen, T Mustonen, MR Hasan, M Takatalo, Y Kobayashi, DA Kesper, A Vortkamp, DP Rice
Front Physiol, 2017-12-19;8(0):1036.
Species: Mouse
Sample Types: Whole Cells
Applications: Bioassay -
Endogenously produced Indian Hedgehog regulates TGFbeta-driven chondrogenesis of human bone marrow stromal/stem cells.
Authors: Handorf A, Chamberlain C, Li W
Stem Cells Dev, 2015-01-26;24(8):995-1007.
Species: Human
Sample Types: Whole Cells
Applications: Bioassay -
The osteoblast to osteocyte transition: epigenetic changes and response to the vitamin D3 hormone.
Authors: St John, Hillary, Bishop, Kathleen, Meyer, Mark B, Benkusky, Nancy A, Leng, Ning, Kendziorski, Christin, Bonewald, Lynda F, Pike, J Wesley
Mol Endocrinol, 2014-05-30;28(7):1150-65.
Species: Mouse
Sample Types: Whole Cells
Applications: Bioassay -
Chondrocyte proliferation regulated by secreted luminal domain of ER stress transducer BBF2H7/CREB3L2.
Authors: Saito A, Kanemoto S, Zhang Y, Asada R, Hino K, Imaizumi K
Mol Cell, 2013-12-12;53(1):127-39.
Species: Human
Sample Types: Cell Culture Supernates
Applications: Bioassay -
Plasma Shh Levels Reduced in Pancreatic Cancer Patients
Authors: Mohamad El-Zaatari, Stephanie Daignault, Art Tessier, Gail Kelsey, Lisa A. Travnikar, Esperanza F. Cantu et al.
Pancreas
Species: Human
Sample Types: Plasma, Whole Cells
Applications: Bioassay, ELISA Standard -
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 -
Signaling hierarchy regulating human endothelial cell development.
Authors: Kelly MA, Hirschi KK
Arterioscler. Thromb. Vasc. Biol., 2009-02-12;29(5):718-24.
Species: Human
Sample Types: Whole Cells
Applications: Bioassay
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