Recombinant Human CD151 Fc Chimera Protein, CF

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When Recombinant Human Integrin alpha V beta 3 (Catalog # 3050-AV) isimmobilized at 1 μg/mL, 100 μL/well, Recombinant Human CD151 Fc Chimera bindswith an ED50 of 0.3‑1.8 μg/mL.
2 μg/lane of Recombinant Human CD11b/Integrin alpha M was resolved with SDS-PAGE underreducing (R) and non-reducing (NR) conditions and visualized by Coomassie® Bluestaining, showing bands at 41-55 kDa and 80 - ...read more

Product Details

Summary
Reactivity HuSpecies Glossary
Applications Bioactivity
Format
Carrier-Free

Order Details

Recombinant Human CD151 Fc Chimera Protein, CF Summary

Details of Functionality
Measured by its binding ability in a functional ELISA. When Recombinant Human Integrin  alpha V beta 3 (Catalog # 3050-AV) is immobilized at 1 μg/mL, 100 μL/well, Recombinant Human CD151 Fc Chimera binds with an ED50 of 0.3-1.8 μg/mL.  
Source
Chinese Hamster Ovary cell line, CHO-derived human CD151 protein
MDHuman IgG1
(Pro100-Lys330)
IEGR Human CD151-LEL
(Ala113-Arg221)
Accession # P48509
N-terminusC-terminus
Accession #
N-terminal Sequence
Met
Structure / Form
Disulfide-linked homodimer
Protein/Peptide Type
Recombinant Proteins
Purity
>95%, by SDS-PAGE visualized with Silver Staining and quantitative densitometry by Coomassie® Blue Staining.
Endotoxin Note
<0.10 EU per 1 μg of the protein by the LAL method.

Applications/Dilutions

Dilutions
  • Bioactivity
Theoretical MW
39 kDa.
Disclaimer note: The observed molecular weight of the protein may vary from the listed predicted molecular weight due to post translational modifications, post translation cleavages, relative charges, and other experimental factors.
SDS-PAGE
41-55, and 90-102 kDa (non-reducible dimer), reducing conditions

Packaging, Storage & Formulations

Storage
  • 12 months from date of receipt, ≤ -20 °C as supplied.
  • 1 month, 2 to 8 °C under sterile conditions after reconstitution.
  • 3 months, ≤ -20 °C under sterile conditions after reconstitution.
Buffer
Lyophilized from a 0.2 μm filtered solution in PBS.
Purity
>95%, by SDS-PAGE visualized with Silver Staining and quantitative densitometry by Coomassie® Blue Staining.
Reconstitution Instructions
Reconstitute at 500 μg/mL in PBS.

Notes

This product is produced by and ships from R&D Systems, Inc., a Bio-Techne brand.

Alternate Names for Recombinant Human CD151 Fc Chimera Protein, CF

  • CD151 antigen (Raph blood group)
  • CD151 antigenplatelet surface glycoprotein gp27
  • CD151 molecule (Raph blood group)
  • CD151
  • GP27
  • Membrane glycoprotein SFA-1
  • MER2
  • PETA3
  • PETA-3
  • PETA-3SFA-1
  • platelet-endothelial cell tetraspan antigen 3
  • Platelet-endothelial tetraspan antigen 3
  • RAPH
  • SFA1
  • SFA-1
  • tetraspanin-24
  • TSPAN24
  • tspan-24
  • TSPAN24hemidesmosomal tetraspanin CD151

Background

Human CD151, also known as SFA-1, Tetraspanin-24, and GP27, is a palmitoylated glycoprotein in the tetraspanin superfamily. It is the first tetraspanin member to be identified as a promoter of cancer metastasis (1, 2), and it is found to participate in nearly all stages of cancer progression (3). CD-151 is normally expressed in endothelial cells, platelets, and frequently over-expressed in cancer cells (4). Mature CD-151 is a multi-pass membrane protein that contains four transmembrane domains, three cytoplasmic domains, and two extracellular loops. The region of amino acids (aa) 113-221 contains the largest extracellular loop (LEL) that involves in interacting with integrins and regulating integrin functions (5). Human CD151 LEL shares 88.9% and 87.0% aa identity with that of mouse and rat respectively. CD151 interacts with integrins such as alpha v beta 3, alpha 3 beta 1, alpha 6 beta 1, alpha 7 beta 1, and alpha 6 beta 4 to regulate their activities and thus resulting in modulation of adhesion, spreading, migration, angiogenesis, invasion and metastasis (1, 3-5). CD151 can also complex with immunoglobulin super family proteins and other tetraspanins such as CD9, CD81, and CD63 (3). Clinically, high levels of CD151 are correlated with poor prognosis in a variety of tumors (3, 4). CD151 has been implicated as a potential diagnostic marker in osteosarcoma and prostate cancer and a putative target for antibody-based immunotherapy (3). CD-151 is a key player in the formation of basement membranes in kidney and skin tissues; it is also associated with human papillomavirus (HPV) infection (6, 7).
  1. Detchokul, S. et al. (2014) Br. J. Pharmacol. 171(24):5462.
  2. Hasegawa, H. et al. (1996). Journal of Virology 70: 3258.
  3. Sadej, R. et al. (2014) Laboratory Investigation 94:41.
  4. Kumari, S. et al. (2015) Biomark Cancer 7:7.
  5. Yu J. et al. (2017) Biochem. J. 474(4):589.
  6. Scheffer, K.D. et al. (2014) Viruses 6:893.
  7. Karamatic Crew, V. et al. (2004) Blood 104:2217.

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