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Recombinant Rat CD36 protein (rFc Tag)

Species

Rat

Purity

>90 %, SDS-PAGE

Tag

rFc Tag

Activity

not tested

Cat no : Eg3222

Validation Data Gallery

  • Purity of Recombinant Rat CD36 was determined by SDS-PAGE. The protein was resolved in an SDS-PAGE in reducing (R) and non-reducing (NR) conditions and stained using Coomassie blue.

    Purity of Recombinant Rat CD36 was determined by SDS-PAGE. The protein was resolved in an SDS-PAGE in reducing (R) and non-reducing (NR) conditions and stained using Coomassie blue.

Product Information

Purity >90 %, SDS-PAGE
Endotoxin <0.1 EU/μg protein, LAL method
Activity 
Not tested
Expression HEK293-derived Rat CD36 protein Gly30-Lys439 (Accession# Q07969) with a rabbit IgG Fc tag at the C-terminus.
GeneID 29184
Accession Q07969
PredictedSize 72.6 kDa
SDS-PAGE 85-110 kDa, reducing (R) conditions
Formulation Lyophilized from 0.22 μm filtered solution in PBS, pH 7.4. Normally 5% trehalose and 5% mannitol are added as protectants before lyophilization.
Reconstitution Briefly centrifuge the tube before opening. Reconstitute at 0.1-0.5 mg/mL in sterile water.
Storage Conditions
It is recommended that the protein be aliquoted for optimal storage. Avoid repeated freeze-thaw cycles.
  • Until expiry date, -20℃ to -80℃ as lyophilized proteins.
  • 3 months, -20℃ to -80℃ under sterile conditions after reconstitution.
Shipping The product is shipped at ambient temperature. Upon receipt, store it immediately at the recommended temperature.

Background

CD36 is widely recognized as a plasma membrane protein. On the cell membrane, CD36 and caveolin-1 can co-polymerize in plasma membrane domains called caveolae, which are specialized cell-membrane microdomains that are rich in cholesterol, sphingomyelin, signaling molecules, and receptor proteins and promote the integration of signaling cascades. CD36 can be transported to organelle and cell membranes by intracellular and extracellular vesicles and can regulate FA uptake and the balance of energy metabolism.

References:

1. Glatz JF. et al. (2010). Physiol Rev. 90:367–417.
2. Lamaze C. et al. (2017). Curr Opin Cell Biol. 47:117–25.
3. Wang J. et al. (2019). Theranostics. 9(17):4893-4908.