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Cell Signaling Technology

Orders: 877-616-CELL (2355) [email protected]

Support: 877-678-TECH (8324)

Web: [email protected] cellsignal.com

3 Trask LaneDanversMassachusetts01923USA
For Research Use Only. Not for Use in Diagnostic Procedures.
MW (kDa):

50

UniProt ID:

#P17936

Entrez-Gene Id:

3486

Background

IGFBP3 is a multifunctional protein that plays a key role in regulation of IGFI/II activity, cell proliferation, and death. One of six high-affinity IGF binding proteins, IGFBP3 is the major species in circulation and is bound in a complex with ALS to 99% of hepatic IGF-I (1). Proteolytic degradation of IGFBP3 increases the bioavailability and activity of the IGF I/II (1). However, some biological activities of IGFBP3 are independent of the IGF/IGF-IR axis. IGFBP3 potentiates EGF-induced breast cancer cell proliferation in vitro by enhancing ERK phosphorylation and sphingosine kinase-mediated EGFR trans-activation (2,3). Conversely, IGFBP3 has been shown to induce apoptosis and inhibit NF-κB activity (4).

  1. Jogie-Brahim, S. et al. (2009) Endocr Rev 30, 417-37.
  2. Martin, J.L. et al. (2003) J Biol Chem 278, 2969-76.
  3. Martin, J.L. et al. (2009) J Biol Chem 284, 25542-52.
  4. Han, J. et al. (2011) Cancer Lett 307, 200-10.

Endotoxin

Less than 0.01 ng endotoxin/1 μg hHis6IGFBP3.

Purity

>95% as determined by SDS-PAGE of 6 μg reduced (+) and nonreduced (-) recombinant hHisIGFBP3. All lots are greater than 95% pure.

Source / Purification

Recombinant Human His6IGFBP3 (hHis6IGFBP3) Gly28-Lys291 (Accession #NP_17936) was expressed in human 293 cells at Cell Signaling Technology.

Bioactivity

The bioactivity of hHis6IGFBP3 was determined by inhibition of IGF-I induced AKT phosphorylation in human dermal fibroblasts. The ED50 of each lot is between 2.5-9 ng/ml.

Background

IGFBP3 is a multifunctional protein that plays a key role in regulation of IGFI/II activity, cell proliferation, and death. One of six high-affinity IGF binding proteins, IGFBP3 is the major species in circulation and is bound in a complex with ALS to 99% of hepatic IGF-I (1). Proteolytic degradation of IGFBP3 increases the bioavailability and activity of the IGF I/II (1). However, some biological activities of IGFBP3 are independent of the IGF/IGF-IR axis. IGFBP3 potentiates EGF-induced breast cancer cell proliferation in vitro by enhancing ERK phosphorylation and sphingosine kinase-mediated EGFR trans-activation (2,3). Conversely, IGFBP3 has been shown to induce apoptosis and inhibit NF-κB activity (4).

Background References

    Cross-Reactivity Key

    H: human M: mouse R: rat Hm: hamster Mk: monkey Vir: virus Mi: mink C: chicken Dm: D. melanogaster X: Xenopus Z: zebrafish B: bovine Dg: dog Pg: pig Sc: S. cerevisiae Ce: C. elegans Hr: horse GP: Guinea Pig Rab: rabbit All: all species expected

    Trademarks and Patents

    Cell Signaling Technology is a trademark of Cell Signaling Technology, Inc.
    PathScan is a trademark of Cell Signaling Technology, Inc.
    All other trademarks are the property of their respective owners. Visit cellsignal.com/trademarks for more information.

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    Revision 1
    #12579

    Human His6IGFBP3 (hHis6IGFBP3)

    Human His6IGFBP3 (hHis6IGFBP3): Image 1 Expand Image
    IGF-I 诱导 hHis6IGFBP3 磷酸化 Akt 受到抑制。在 hHis6IGFBP3 的浓度不断升高或不升高的情况下,人皮肤成纤维细胞使用 Human Insulin-like Growth Factor I (hIGF-I) # 8917 处理 10 分钟,裂解后,使用 PathScan® Phospho-Akt1 (Ser473) Sandwich ELISA Kit #7160 对 Akt1 (Ser473) 磷酸化进行定量分析。
    Human His6IGFBP3 (hHis6IGFBP3): Image 2 Expand Image
    对 6 µg 还原 (+) 和非还原 (-) 重组 hHis6 IGFBP3 进行 SDS-PAGE 并使用考马斯蓝染色过夜

    来测定重组 His6 IGFBP3 的纯度。