Recombinant human PEDF/Serpin-F1 (HEK expressed) protein

(HB7366)
Technical documents: Datasheet

Product overview

Name Recombinant human PEDF/Serpin-F1 (HEK expressed) protein
Alternative names Recombinant Human Pigment Epithelium-Derived Factor, HEK, Pigment epithelium-derived factor, PEDF, Serpin-F1, SerpinF1, EPC-1, EPC1, PIG35.
Purity >95%
Description HEK expressed recombinant human PEDF/Serpin-F1 protein
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Solubility & Handling

Solubility overview To make a working stock solution, add deionized water to make a solution (0.5mg/mL) and allow the lyophilized material to dissolve. Filter the product using an appropriate sterile filter before using it in cell culture
Handling
  • Solutions should be made in sterile deionized water (not less than 100 µg/ml). This solution can then be further diluted with other aqueous solutions.
  • Following reconstitution, solutions may be stored at 4°C and are useable for around 2-7 days and for future use store at -18°C.
  • Freeze-thaw cycles should be prevented.
Important This product is for RESEARCH USE ONLY and is not intended for therapeutic or diagnostic use. Not for human or veterinary use.

Calculators

Molarity

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Dilution

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Chemical Data

Purity >95%
Source HEK 293.
Appearance White lyophilized powder (filtered & freeze-dried)
Formulation Lyophilized from filtered (0.4μm) solution (0.5mg/ml) containing Tris (20mM) & NaCl pH 7.5 (20mM)

References for Recombinant human PEDF/Serpin-F1 (HEK expressed) protein

References are publications that support the biological activity of the product
  • PEDF and its roles in physiological and pathological conditions: implication in diabetic and hypoxia-induced angiogenic diseases

    He X et al (2015) Clin Sci (Lond) 128(11) : 805-23
  • Pigment epithelium-derived factor (PEDF) is one of the most abundant proteins secreted by human adipocytes and induces insulin resistance and inflammatory signaling in muscle and fat cells

    Famulla S et al (2011) Int J Obes (Lond) 35(6) : 762-72
  • PEDF: a multifaceted neurotrophic factor

    Tombran-Tink J et al (2003) Nat Rev Neurosci 4(8) : 628-36

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