R&D Systems代理4106-RS-025 Recombinant Mouse R-Spondin 4 Protein (25 UG)

2025-06-25

货号:4106-RS-025

品牌:R&D Systems

规格:25ug

目录价:¥4490.00

市场价格:¥3592.00

会员价格:¥3592.00

  • 到货时间:3~4周

    金山科研平台,产品价格货期咨询微信:jinshanbio Source:Chinese Hamster Ovary cell line, CHO-derived, Ala19-Gln228 Accession #:Q8BJ73 N-terminal Sequence Analysis:Ala19 Purity:>95%, by SDS-PAGE under reducing conditions and visualized by silver stain. Predicted Molecular Mass:23.9 kDa SDS-PAGE:32 kDa, reducing conditions Activity:Measured by its ability to induce activation of beta -catenin response in a Topflash Luciferase assay using HEK293T human embryonic kidney cells.The ED50 for this effect is typically5 -20 ng/mL in the presence of10 ng/mL rmWnt-3a. Molecule Information: R-Spondin 4 Long Name: Roof Plate-specific Spondin 4 Aliases: Cristin 4; RSPO4 Entrez Gene IDs: 343637 (Human); 228770 (Mouse) Background: R-Spondin 4 R-Spondin 4 (RSPO4, roof plate-specific spondin 4), also called cysteine-rich and single thrombospondin domain containing-4 (Cristin 4), is an ~33 kDa secreted heparin-binding protein that shares ~35% amino acid (aa) identity with three other R-Spondin family members. All are positive modulators of Wnt/beta-Catenin signaling, but vary in activity. R-Spondins regulate Wnt/beta-Catenin by competing with the Wnt antagonist DKK-1 for binding to the Wnt co-receptors LRP-6 and Kremen, reducing their DKK-1-mediated internalization. Like other R-spondins, human R-Spondin 4 (228 aa) contains a signal sequence (aa 1-19), two adjacent cysteine-rich furin-like domains (aa 85-128) with one potential tyrosine phosphorylation site (aa 114), followed by a thrombospondin (TSP-1) motif (aa 137-197) and a region rich in basic residues (aa 199-228). Mature human R-Spondin 4 shares 81%, 81%, 84%, 84% and 86% aa identity with mouse, rat, equine, canine and bovine R-Spondin 4, respectively. Of two potential isoforms, one lacks the TSP-1 domain, while another terminates at aa 224. Each R-Spondin has a distinct expression pattern. In the mouse, R-Spondin 4 mRNA is found during development of limb bud mesenchyme, nail beds, heart and teeth. In humans, mutations of R-Spondin 4 have been found to cause anonychia, a condition in which fingernails and toenails are absent.

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