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

种属

Mouse

纯度

>90 %, SDS-PAGE

标签

His Tag

生物活性

未测试

Cat no : Eg0482

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Synonyms

CD54, Icam-1, ICAM 1, Icam1, MALA-2



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 Mouse ICAM-1 protein Gln28-Asn485 (Accession# P13597-1) with a His tag at the C-terminus.
基因ID 15894
蛋白编号 P13597-1
预测分子量 51 kDa
SDS-PAGE 70-100 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

Intercellular adhesion molecule 1 (ICAM-1, also known as 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. ICAM-1 can exist as membrane-bound form (mICAM-1) and soluble form (sICAM-1). The sICAM-1 arises from alternative splicing and proteolysis of mICAM-1 and appears to be associated with leukocyte activation to produce LFA-1.

参考文献:

1. Lawson C, et al. (2009). Pharmacol Rep. 61(1):22-32. 2. Dustin ML, et al. (1986). J Immunol. 137(1):245-54. 3. Marlin SD, et al. (1987). Cell. 51(5):813-9. 4. Staunton DE, et al. (1989). Cell. 56(5):849-53. 5. Berendt AR, et al. (1989). Nature. 341(6237):57-9. 6. Ramos TN, et al. (2014). J Immunol. 192(10):4469-4474.