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Mouse Recombinant TMEM173 (Prokaryotic) (from E. coli)
Mouse Recombinant TMEM173 (Prokaryotic) (from E. coli)
Catalog # MSPP-RPN011MU1
CAS Number:  
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Mouse Recombinant TMEM173 (Prokaryotic) (from E. coli)
Catalog # MSPP-RPN011MU1
Supplier Number:  RPN011MU01
CAS Number:  

Specifications

  • Pack type:
    Vial
  • Conjugation:
    Unconjugated
  • Protein Function:
    Cytokines and Growth Factors
  • Protein/Peptide Type:
    Recombinant
  • Source:
    E. coli
  • Species:
    Mouse
  • Size:
    50 µg
  • Tag sequence:
    MGHHHHHHSGSEF
  • Storage Conditions:
    –20 °C
  • Endotoxin Content:
    <1.0 EU per 1 μg (determined by the LAL method)
  • Gene ID:
    72512
  • Reconstitution Instructions:
    Reconstitute in 10 mM PBS (pH 7.4) to a concentration of 0.1 - 1.0 mg/ml. Do not vortex.
  • Endotoxin-free:
    N
  • Carrier-Free:
    Y
  • Protease-free:
    N
  • Animal-Free:
    Y
  • Protein Synonyms:
    Transmembrane Protein 173
  • UniProtKB:
    Q3TBT3
  • Protein/Peptide Name:
    TMEM173
  • Purity:
    97 - 100%
  • Molecular Weight:
    28 kDa
  • Sequence:
    Trp160~Leu371
  • Endotoxin Level:
    Low
  • Concentration:
    0.2 mg/ml
  • Formulation:
    Lyophilized from PBS, pH 7.4, containing 0.01% SKL, 5% Trehalose.
  • Nuclease-free:
    N
  • Shipping Temperature:
    4 °C
  • Tested Applications:
    Positive control, Immunogen, SDS-PAGE, Western blot.
  • Cat. No.:
    MSPP-RPN011MU1

Specifications

About this item

This is a TMEM173 recombinant protein (prokaryotic), Mouse is sequencing from Trp160~Leu371 with 97 - 100% purity. Lyophilized from PBS, pH 7.4, containing 0.01% SKL, 5% Trehalose with 0.2 mg/ml.

  • High quality, purity, reproducibility and effectiveness
  • Offers customized buffers and tag options
  • 100% quality and service satisfaction guarantee

The deduced 379-amino acid protein has a calculated molecular mass of 42.2 kDa. It has 5 putative N-terminal transmembrane domains, a signal cleavage site in the first transmembrane domain, and a leucine-rich region that overlaps the first 4 transmembrane domains. Northern blot analysis detected STING expression in all tissues examined. Confocal microscopy and fractionation analysis of human embryonic kidney 293 cells revealed that STING predominantly associated with the endoplasmic reticulum (ER). Western blot analysis of 293 cells detected endogenous STING at an apparent molecular mass of 42 kDa. STING activated both the NF-kappa-B and IRF3 transcription pathways to induce expression of IFN-alpha (IFNA1) and IFN-beta and exert a potent antiviral effect.

Certifications: ISO 9001 and ISO 13485 certified, three level QC system.
Caution: For research use only. Not for use in clinical diagnostic procedures. Please proper stored each component based on the instruction.