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IGFBP-6 Protein, Mouse

IGFBP-6 Protein, Mouse

Catalog Number: UA040535 Brand: UA BIOSCIENCE
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Regular price $120 USD
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Product Details

Product Specification


Species Mouse
Synonyms Insulin-like growth factor-binding protein 6, IBP-6, IGF-binding protein 6, IGFBP-6
Accession P47880
Amino Acid Sequence

Ala26-Gly238 with His Tag at the C-Terminus

Expression System HEK293
Molecular Weight

30-35 kDa (Reducing)

Purity >95% by SDS-PAGE & HPLC.
Endotoxin <0.1EU/μg
Conjugation Unconjugated
Tag His Tag
Physical Appearance Lyophilized powder
Storage Buffer

PBS, 1mM EDTA, pH7.4

Reconstitution

Reconstitute at 0.1-1 mg/ml according to the size in ultrapure water after rapid centrifugation.

Stability & Storage

·12 months from date of receipt, lyophilized powder stored at -20 to -80℃.
·3 months, -20 to -80℃ under sterile conditions after reconstitution.
·1 week, 2 to 8℃ under sterile conditions after reconstitution.
·Please avoid repeated freeze-thaw cycles.

Reference

J Clin Invest. 2008 Jul;118(7):2609-19.
Growth Horm IGF Res. 2016 Oct-Dec:30-31:81-86.

Background

Insulin-like Growth Factor Binding Protein-6 (IGFBP-6) is a 30-kDa secreted glycoprotein encoded by the Igfbp6 gene, distinguished by its extraordinary ~50–70-fold binding preference for IGF-II over IGF-I. This selectivity is mediated by cooperative interactions between the N-terminal subdomain and C-terminal domain of IGFBP-6 with adjacent binding sites on IGF-II. IGFBP-6 primarily functions as a selective inhibitor of IGF-II actions, blocking IGF-II-induced cell proliferation, differentiation, migration, and survival across diverse cell types including myoblasts, neuroblastoma cells, and rhabdomyosarcoma cells. Unlike other IGFBPs, it has minimal effect on IGF-I activity.

IGFBP-6 expression is developmentally regulated in mouse skeletal muscle, with high levels during embryogenesis and sustained expression in adult muscle tissue. In aging mice, serum IGFBP-6 levels increase progressively. Expression is regulated by TGF-β (via SMAD2/3), hedgehog signaling, p53, and hypoxia-inducible factors.

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Bioactivity

Measured by its ability to inhibit the biological activity of IGF-I or IGF-II on MCF‑7 human breast cancer cells. The EC50 is 0.286-0.831 μg/mL in the presence of 14 ng/mL human IGF-II.

SDS-PAGE

2μg (R: reducing condition, N: non-reducing condition).

RP-HPLC

>95% as determined by RP-HPLC.