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Human IFN gamma Animal-Free Recombinant Protein

 Human IFN gamma Animal-Free Recombinant Protein
 Human IFN gamma Animal-Free Recombinant Protein
 Human IFN gamma Animal-Free Recombinant Protein
New
 Human IFN gamma Animal-Free Recombinant Protein
 Human IFN gamma Animal-Free Recombinant Protein
 Human IFN gamma Animal-Free Recombinant Protein
Human IFN gamma Animal-Free Recombinant Protein
$20.00
Ex Tax: $20.00
  • Stock: In Stock
  • Model: 0681

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Product Description

IFN-γ, an acid-labile interferon, is produced by CD4 and CD8 T lymphocytes as well as activated NK cells. Its receptors are widespread in immune cells, triggering an increase in class I MHC protein surface expression upon IFN-γ signaling. This enhancement aids in antigen presentation to T-helper (CD4+) cells. IFN-γ signaling in antigen-presenting cells, B and T lymphocytes involved in antigen recognition, plays a crucial role in regulating the antigen-specific phases of the immune response. Moreover, IFN-γ stimulates various functions in lymphoid cells, including the anti-microbial and anti-tumor responses of macrophages, NK cells, and neutrophils. Notably, Human IFN-γ is species-specific and exhibits biological activity exclusively in Human and primate cells. Recombinant Human IFN-γ is a 16.8 kDa protein composed of 144 amino acid residues.

 

Product Specifications

 
Species Human
Published species

Bacteria, Fish, Human, Mouse, Rat, Virus

Expression System E. coli
Amino acid sequence

MQDPYVKEAE NLKKYFNAGH SDVADNGTLF LGILKNWKEE SDRKIMQSQI VSFYFKLFKN FKDDQSIQKS VETIKEDMNV KFFNSNKKKR DDFEKLTNYS VTDLNVQRKA IHELIQVMAE LSPAAKTGKR KRSQMLFQGR RASQ

Molecular weight 16.8 kDa
Class Recombinant
Type Protein
Purity

≥ 98% by SDS-PAGE gel and HPLC analyses.

Endotoxin concentration <0.1 EU/µg
Activity

The ED50 determined by a cytotoxicity assay using HT-29 cells. The ED50 is 0.26-0.40 ng/ml. 

Conjugate Unconjugated
Form Lyophilized
Contains

no preservative

Storage conditions -20°C

CAUTION

For Research Use Only. Not for use in diagnostic procedures.

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