WB result of Invivo anti-Mouse CD54 (ICAM-1) Recombinant mAb
Primary antibody: Invivo anti-Mouse CD54 (ICAM-1) Recombinant mAb at 1/1000 dilution
Lane 1: ICAM-1/CD54 His Tag Protein, Mouse lysate 1 µg
Lane 2: ICAM-1/CD54 His Tag Protein, Human lysate 1 µg
Secondary antibody: Goat Anti-Rat IgG (H+L), HRP conjugated at 1/10000 dilution
Predicted MW: 72 kDa
Observed MW: 72 kDa
Product Details
Product Details
Product Specification
| Host | Rat |
| Antigen | CD54 (ICAM-1) |
| Synonyms | Intercellular adhesion molecule 1; MALA-2; MyD10; Icam1 |
| Location | Cell membrane |
| Accession | P13597 |
| Antibody Type | Rat mAb |
| Isotype Control | S0B0997 |
| Application | WB, in vivo neutralization |
| Purification | Protein G |
| Concentration | 5 mg/ml |
| Purity | >95% (Determined by SDS-PAGE) |
| Endotoxin | <1EU/mg |
| Conjugation | Unconjugated |
| Physical Appearance | Liquid |
| Storage Buffer | PBS pH7.4, containing no preservative |
| Stability & Storage | 2 to 8 °C for 2 weeks under sterile conditions; |
Dilution
| application | dilution | species |
| WB | 1:1000 | Ms |
Background
CD54, commonly known as Intercellular Adhesion Molecule-1 (ICAM-1), is a type I transmembrane glycoprotein belonging to the immunoglobulin superfamily that plays a pivotal role in immune responses and inflammation by mediating cell-cell adhesion through high-affinity binding to β2 integrins such as LFA-1 (CD11a/CD18) and Mac-1 (CD11b/CD18) on leukocytes. Expressed constitutively at low levels on endothelial cells and various leukocytes but rapidly upregulated by pro-inflammatory cytokines like TNF-α and IL-1, ICAM-1 facilitates critical physiological processes including leukocyte extravasation across the vascular endothelium, antigen presentation via the immunological synapse between T cells and antigen-presenting cells, and lymphocyte homing. Beyond its essential immune functions, CD54 serves as the primary cellular receptor for human rhinoviruses and certain strains of Plasmodium falciparum-infected erythrocytes, linking it directly to infectious pathogenesis, while its aberrant overexpression is implicated in autoimmune disorders, atherosclerosis, transplant rejection, and tumor metastasis, making it a significant biomarker and therapeutic target for modulating inflammatory and malignant diseases.
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Western Blot
