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Interleukin-6 Human or Mouse Interleukin-6 (IL-6) is a
pro-inflammatory cytokine that also has an important role in immunity. IL-6
induces growth and terminal differentiation of B cells; secretion of immunoglobulins; differentiation and activation of T cells
and macrophages; and the induction of acute-phase response proteins. Many
types of cells, including macrophages, T cells, fibroblasts, and endothelial
cells, produce IL-6 in response to stimuli such as bacteria, viruses, and
other cytokines, particularly IL-1 and tumor necrosis factor, alpha (TNF).
Human IL-6 is active on both mouse and rat cells, while mouse IL-6 has no
activity on human cells. Recombinant human IL-6 is a 22 kDa
protein containing 189 amino acid residues Products
Formulation: Lyophilized powder
lyophilized from a volatile
buffer
(50 mM NH4HCO3
, pH 8.0). Preservative: None. MW: 21 kD Purity: >97% on 15% SDS-PAGE. Source: Recombinant mature protein expressed in E. coli (189 amino acid residues). Sterility: 0.2 µm membrane-filtered and packaged
aseptically. ED50: ND Endotoxin*: ≤0.1 EU/mg. Endotoxin
Unit is determined by Limulus Amebocyte Lysate (LAL) assay (Sigma) Receiving and Storage Upon receiving, store the product at -20oC. After reconstitution, store the working
aliquots at 2-8oC for no more than 3 months. For extended storage,
aliquot the solution (≥100μg/ml) and freeze at -70oC or
-20oC. Avoid repeated freezing and thawing. More dilute solutions
stored at -20oC will lose activity faster. |
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Cloning
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Mutagenesis
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Manuals
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Phone:(858) 457-3658 Fax:(858) 457-3485 Emails |
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Reconstitution and Use Reconstitute the contents of the vial using
sterile phosphate-buffered saline (PBS) to a concentration no less than 100μg/ml
and aliquot for future use. (If the initial rehydration
is too dilute, activity may be lost due to the non-specific adsorption to the
container). The solution can then be further
diluted to a working stock solution. If the product is going to be used for
applications requiring absolute asepsis, it’s best to filter-sterilize the
solution using a sterile and non-pyrogenic 0.2µm
membrane before use. References Kishimoto,
T. (1989) Blood 74:1. Barton, B.E. (1997) Clin.
Immunol. Immunopathol.
85:16. Poupart,
P. et al. (1987) EMBO J. 6:1219. Hibi,
M. et al. (1996) J. Mol. Med. 74:1. Hirano, T. et al. (1994) Stem Cells
12:262. Akira, S. et al. (1993) Adv. Immunol. 54:1. Van Snick, J. (1990) Annu.
Rev. Immunol. 8:253. Kishimoto,
T. et al. (1992) Polyfunctional Cytokines: IL-6 and
LIF. Wiley, Kishimoto,
T. (1992) Int. Arch. Allergy Immunol. 99:172. Chiu, C-P. et al.
(1988) Proc. Natl. Acad. Sci. USA 85:7099. Northemann,
W. et al. (1989) J. Biol. Chem. 264:16072 |
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