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Ä«Å×°í¸® Cytokines & Growth Factor
CAT.NO LGP-12-076
PRODUCT IFN-¥ã, Mouse (Murine Interferon-gamma)
SIZE 100ug, 500ug, 1mg
PRICE KRW 285,000, 940,000, 1,570,000
Technical Parameters
Accession P01580
GeneID 15978
Source Escherichia coli.
Molecular Weight Approximately 15.5 kDa, a single non-glycosylated polypeptide chain containing 133 amino acids.
Quantity 100µg/500µg/1000µg
AA Sequence HGTVIESLES LNNYFNSSGI DVEEKSLFLD IWRNWQKDGD MKILQSQIIS FYLRLFEVLK DNQAISNNIS VIESHLITTF FSNSKAKKDA FMSIAKFEVN NPQVQRQAFN ELIRVVHQLL PESSLRKRKR SRC
Purity > 96 % by SDS-PAGE and HPLC analyses.
Biological Activity Fully biologically active when compared to standard. The ED50 as determined by an anti-viral assay using murine L929 cells infected with encephalomyocarditis (EMC) virus is less than 0.8 ng/ml, corresponding to a specific activity of > 1.3 ¡¿ 106 IU/mg.
Physical Appearance Sterile Filtered White lyophilized (freeze-dried) powder.
Formulation Lyophilized from a 0.2 µm filtered solution in PBS, pH 7.4, containing 5 % trehalose.
Endotoxin Less than 1 EU/µg of rMuIFN-¥ã as determined by LAL method.
Reconstitution We recommend that this vial be briefly centrifuged prior to opening to bring the contents to the bottom. Reconstitute in sterile distilled water or aqueous buffer containing 0.1 % BSA to a concentration of 0.1-1.0 mg/ml. Stock solutions should be apportioned into working aliquots and stored at ¡Â -20 ¡ÆC. Further dilutions should be made in appropriate buffered solutions.
Stability & Storage Use a manual defrost freezer and avoid repeated freeze-thaw cycles.
- 12 months from date of receipt, -20 to -70 ¡ÆC as supplied.
- 1 month, 2 to 8 ¡ÆC under sterile conditions after reconstitution.
- 3 months, -20 to -70 ¡ÆC under sterile conditions after reconstitution.
Usage This material is offered by Korea Lugen Sci for research, laboratory or further evaluation purposes. NOT FOR HUMAN USE.
Reference 1. Pennino D, Bhavsar PK, Effner R, et al. 2012. J Allergy Clin Immunol, 
2. Hibi M, Hachimura S, Ise W, et al. 2003. Cytotechnology, 43: 49-55.
3. Wang H, Ruan Z, Wang Y, et al. 2008. Mol Immunol, 45: 1548-56.
4. Kopinski P, Przybylski G, Jarzemska A, et al. 2007. Pol Merkur Lekarski, 23: 15-21.
Background Interferon-gamma (IFN-¥ã), also known as Type II interferon or immune interferon, is a cytokine produced primarily by T-lymphocytes and natural killer cells. The protein shares no significant homology with IFN-¥â or the various IFN-¥á family proteins. Mature IFN-¥ã exists as noncovalently-linked homodimers. It shares high sequence indentity with rat IFN-¥ã (86 %). IFN-¥ã was originally characterized based on its antiviral activities. The protein also exerts antiproliferative, immunoregulatory and proinflammatory activities and is thus important in host defense mechanisms. IFN-¥ã induces the production of cytokines, upregulates the expression of class I and II MHC antigens, Fc receptor and leukocyte adhesion molecules. It modulates macrophage effector functions, influences isotype switching and potentiates the secretion of immunoglobulins by B cells. Additionally, IFN-¥ã augments TH1 cell expansion and may be required for TH1 cell differentiation.

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