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Recombinant Rat ICAM-1/CD54 protein (His Tag)

种属

Rat

纯度

>90 %, SDS-PAGE

标签

His Tag

生物活性

未测试

Cat no : Eg1025

Print datasheet

Synonyms

CD54, ICAM-1, ICAM-1/CD54, Icam1

验证数据展示

  • Purity of Recombinant Rat ICAM-1 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 ICAM-1 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.

产品信息

纯度 >90 %, SDS-PAGE
内毒素 <0.1 EU/μg protein, LAL method
生物活性 Not tested
来源 HEK293-derived Rat ICAM-1 protein Gln28-Thr493 (Accession# Q00238) with a His tag at the C-terminus.
基因ID 25464
蛋白编号 Q00238
预测分子量 52.2 kDa
SDS-PAGE 65-85 kDa, reducing (R) conditions
组分 Lyophilized from 0.22 μm filtered solution in PBS, pH 7.4. Normally 5% trehalose and 5% mannitol are added as protectants before lyophilization.
复溶 Briefly centrifuge the tube before opening. Reconstitute at 0.1-0.5 mg/mL in sterile water.
储存条件
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.
运输条件 The product is shipped at ambient temperature. Upon receipt, store it immediately at the recommended temperature.

背景信息

ICAM-1 (CD54) is a transmembrane glycoprotein of the immunoglobulin superfamily and is critical for the firm attachment and transmigration of leukocytes out of blood vessels and into tissues. ICAM-1 is expressed by several cell types, typically on endothelial cells and cells of the immune system, and its expression can be up-regulated by various stimuli, including TNF-α, INF-γ, IL-1 and thrombin. It is a ligand for LFA-1 and Mac-1, serves as a receptor for rhinovirus, and is one of several receptors used by Plasmodium falciparum.

参考文献:

1. M L Dustin, et al. (1986) J Immunol. 137(1):245-54.
2. C W Smith, et al. (1989) J Clin Invest. 83(6):2008-17.
3. D E Staunton, et al. (1989) Cell. 56(5):849-53. 
4. A R Berendt, et al. (1989) Nature. 341(6237):57-9. 
5. G Kaplanski, et al. (1998) Blood. 92(4):1259-67.
6. Narimasa Miho, et al. (2005) Cardiovasc Res. 68(2):289-98.
7. Charlotte Lawson, et al. (2009) Pharmacol Rep. 61(1):22-32.