Anti-ICAM-3/CD50 Antibody, Rabbit Polyclonal sinobiological 10333-RP02

$143.00
In stock
SKU
10333-RP02
Catalog No.SizePrice (USD)
10333-RP02-5050 µL$147.96
10333-RP02-100100 µL$251.64
10333-RP02-200200 µL$355.32

General Information

Product nameAnti-ICAM-3/CD50 Antibody, Rabbit Polyclonal
Validated applicationsWB (FAQ Protocol), ELISA (FAQ Protocol), IP (FAQ Protocol)
Species reactivityReacts with: Human
SpecificityHuman ICAM-3/CD50
ImmunogenRecombinant Human ICAM3 / CD50 protein (Catalog#10333-H08H)
PreparationProduced in rabbits immunized with purified, recombinant Human ICAM3 / CD50 (rh ICAM3 / CD50; Catalog#10333-H08H; CAA49369.1; Met 1-His 485). ICAM3 / CD50 specific IgG was purified by Human ICAM3 / CD50 affinity chromatography.
SourcePolyclonal Rabbit IgG
PurificationProtein A & Antigen Affinity
Formulation0.2 μm filtered solution in PBS
ConjugateUnconjugated
FormLiquid
ShippingThis antibody is shipped as liquid solution at ambient temperature. Upon receipt, store it immediately at the temperature recommended below.
StorageThis antibody can be stored at 2℃-8℃ for one month without detectable loss of activity. Antibody products are stable for twelve months from date of receipt when stored at -20℃ to -80℃. Preservative-Free. Avoid repeated freeze-thaw cycles.

Synonyms: Anti-CD50 Antibody; Anti-CDW50 Antibody; Anti-ICAM-R Antibody

Image / Experimental Information

Image 1 DescriptionAnti-ICAM3 rabbit polyclonal antibody at 1:500 dilution Lane A: HL-60 Membrane Lysate Lysates/proteins at 20 μg per lane. Secondary Goat Anti-Rabbit IgG H&L (Dylight800) at 1/10000 dilution. Developed using the Odyssey technique. Performed under reducing conditions. Predicted band size:60 kDa Observed band size:150 kDa
Image 1 Alt TextHuman ICAM-3 / CD50 Western blot (WB) 13187
Image 1 URLSource image
Image 2 DescriptionAnti-ICAM3 rabbit polyclonal antibody at 1:500 dilution Lane A: HL-60 Membrane Lysate Lysates/proteins at 20 μg per lane. Secondary Goat Anti-Rabbit IgG H&L (Dylight800) at 1/10000 dilution. Developed using the Odyssey technique. Performed under reducing conditions. Predicted band size:60 kDa Observed band size:150 kDa
Image 2 Alt TextHuman CD50 Immunoprecipitation(IP) 30542
Image 2 URLSource image

Background Information

Full Nameintercellular adhesion molecule 3
DescriptionThe protein ICAM-3, also known as CD50, is a member of the intercellular adhesion molecule (ICAM) family consisting of three members. It is a DC-SIGN ligand that is constitutively expressed on resting leukocytes and is thus an important molecule for the first immune response. ICAM-3 comprises five immunoglobulin-like domains and binds LFA-1 through its two N-terminal domains. It functions not only as an adhesion molecule but also as a potent signaling molecule. ICAM-3 binds to LFA-1 on antigen-presenting cells (APC) stabilizing the T cell-APC interaction, facilitating signaling through the CD3/TCR complex. However, recent evidence using cultured and transformed T cells suggests ICAM-3 may also function in signaling. It has been reported that the CD50 molecule can play a role in developing functionally mature T lymphocytes and its expression increases during the maturation process of T lymphocytes. Also, the interactions of ICAM-3 and LFA-1 facilitate HIV-1- induced virological synapse formation between T cells. ICAM-3 is associated with an increase in cellular radio-resistance and cancer cell proliferation. It could be considered as a candidate for anti-cancer drug development and as a cancer diagnostic marker.
References
  1. Berney SM, et al. (1999) ICAM-3 (CD50) cross-linking augments signaling in CD3-activated peripheral human T lymphocytes. J Leukoc Biol. 65(6): 867-74.
  2. van Buul JD, et al. (2004) ICAM-3 activation modulates cell-cell contacts of human bone marrow endothelial cells. J Vasc Res. 41(1): 28-37.
  3. Sugino H. (2005) ICAM-3, a ligand for DC-SIGN, was duplicated from ICAM-1 in mammalian evolution, but was lost in the rodent genome. FEBS Lett. 579(13): 2901-6.
  4. Park JK, et al. (2010) ICAM-3 enhances the migratory and invasive potential of human non-small cell lung cancer cells by inducing MMP-2 and MMP-9 via Akt and CREB. Int J Oncol. 36(1): 181-92.

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