Anti-Human ICAM-1 – Purified in vivo PLATINUM™ Functional Grade

Anti-Human ICAM-1 – Purified in vivo PLATINUM™ Functional Grade

Product No.: C672

[product_table name="All Top" skus="C372"]

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Clone
15.2
Target
ICAM-1
Formats AvailableView All
Product Type
Monoclonal Antibody
Alternate Names
BB2, CD54, P3.58
Isotype
Mouse IgG1
Applications
FC
,
IHC FFPE
,
IP
,
WB

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Antibody Details

Product Details

Reactive Species
Human
Host Species
Mouse
Recommended Dilution Buffer
Immunogen
Human infant thymocytes and Sezary cells
Product Concentration
≥ 5.0 mg/ml
Endotoxin Level
<0.5 EU/mg as determined by the LAL method
Purity
≥98% monomer by analytical SEC
>95% by SDS Page
Formulation
This monoclonal antibody is aseptically packaged and formulated in 0.01 M phosphate buffered saline (150 mM NaCl) PBS pH 7.2 - 7.4 with no carrier protein, potassium, calcium or preservatives added. Due to inherent biochemical properties of antibodies, certain products may be prone to precipitation over time. Precipitation may be removed by aseptic centrifugation and/or filtration.
Product Preparation
Functional grade preclinical antibodies are manufactured in an animal free facility using in vitro cell culture techniques and are purified by a multi-step process including the use of protein A or G to assure extremely low levels of endotoxins, leachable protein A or aggregates.
Pathogen Testing
To protect mouse colonies from infection by pathogens and to assure that experimental preclinical data is not affected by such pathogens, all of Leinco’s Purified Functional PLATINUM™ antibodies are tested and guaranteed to be negative for all pathogens in the IDEXX IMPACT I Mouse Profile.
Storage and Handling
Functional grade preclinical antibodies may be stored sterile as received at 2-8°C for up to one month. For longer term storage, aseptically aliquot in working volumes without diluting and store at ≤ -70°C. Avoid Repeated Freeze Thaw Cycles.
Country of Origin
USA
Shipping
Next Day 2-8°C
Applications and Recommended Usage?
Quality Tested by Leinco
FC
WB
Additional Applications Reported In Literature ?
IHC FFPE
IP
Each investigator should determine their own optimal working dilution for specific applications. See directions on lot specific datasheets, as information may periodically change.

Description

Description

Specificity
Mouse Anti-Human Inter-Cellular Adhesion Molecule 1 (Clone 15.2) recognizes an epitope on Human ICAM-1. This monoclonal antibody was purified using multi-step affinity chromatography methods such as Protein A or G depending on the species and isotype.
Background
ICAM-1 is a 55 kDa glycoprotein that is part of the Ig superfamily. It is heavily glycosylated to form 75 kDa to 115 kDa. ICAM-1 is known to be an adhesion and viral entry molecule, and its long suspected involevement in signal transduction is being elucidated. The signal-transducing functions of ICAM-1 appear to be mainly associated with proinflammatory pathways. Furthermore, ICAM-1 signaling appears to act as a beacon for inflammatory immune cells such as macrophages and granulocytes bringing about inflammation via lymphocyte trafficking. ICAM-1 is essential for the transmigration of leukocytes out of blood vessels and into tissues, and is a marker of endothelial dysfunction leading to damaging vascular disorders in umbilical and placental vascular tissue of gestational pregnancies. ICAM-1 is the receptor for rhinoviruses (the cause of most common colds) and malaria, and plays an inflammatory role in ocular allergies.
Antigen Distribution
CD54 is present on endothelial cells, lymphocytes, epithelial cells, dendritic cells and keratinocytes.
PubMed
NCBI Gene Bank ID

Leinco Antibody Advisor

Powered by AI: AI is experimental and still learning how to provide the best assistance. It may occasionally generate incorrect or incomplete responses. Please do not rely solely on its recommendations when making purchasing decisions or designing experiments.

Clone 15.2 is most commonly used in vivo in mice to block ICAM-1 (CD54)-mediated cellular interactions and investigate inflammatory and immune processes.

Key in vivo applications:

  • Blocking ICAM-1 function: Clone 15.2 is a mouse monoclonal antibody that specifically binds human ICAM-1 (CD54), a cell surface glycoprotein involved in leukocyte adhesion and migration. In mouse models expressing human ICAM-1 (e.g., transgenic or engrafted models), clone 15.2 is administered to inhibit ICAM-1 function, allowing researchers to study its role in inflammation, tissue injury, tumor metastasis, and immune cell trafficking.
  • Investigating inflammation: By blocking ICAM-1 interactions, researchers study the effects on leukocyte extravasation, recruitment, or endothelial activation in models of autoimmune disease, ischemia/reperfusion, and infection.
  • Tumor and metastasis studies: Clone 15.2 may be used to explore how ICAM-1 contributes to tumor cell adhesion, invasion, and metastatic spread in models where human ICAM-1 is present.
  • Transplant and rejection models: In chimeric or xenograft models, clone 15.2 can help dissect ICAM-1’s role in graft-versus-host disease or organ transplant rejection through blockade of leukocyte–endothelial cell interactions.

Additional context:

  • Species specificity: Clone 15.2 primarily recognizes human ICAM-1 and is not generally reactive with endogenous mouse ICAM-1, limiting its standard use in wild-type mice. It is applied in mice that express human ICAM-1 transgenically or in studies involving grafts from human tissues.
  • In vivo functional studies: Antibodies with low endotoxin, such as those produced for in vivo applications, reduce off-target inflammatory effects and are preferred for direct injection into mice.

If you are interested in in vivo applications targeting mouse MHC class II (I-A/I-E), this is a different antibody clone (M5/114.15.2), which is commonly used for blocking antigen presentation in mouse immune models.

The 15.2 antibody is a monoclonal antibody that specifically recognizes ICAM-1 (CD54), a cell surface glycoprotein involved in leukocyte adhesion and signal transduction. In the literature, when 15.2 is used, it is often combined with other antibodies or proteins for multi-parametric analyses or to investigate related cellular processes.

Commonly used antibodies or proteins with 15.2 (anti-ICAM-1):

  • CD44: Frequently paired as both are adhesion molecules relevant in contexts like tumor microenvironments or immune cell interactions.
  • CD45: Used for general leukocyte identification, often included in panels investigating immune cell phenotypes.
  • CD11a/CD18 (LFA-1): LFA-1 is a ligand for ICAM-1, and co-staining helps assess cell–cell adhesion mechanisms.
  • CD31 (PECAM-1): Another endothelial marker, co-stained to distinguish between different adhesion molecules in vascular studies.
  • HLA-DR, CD80, CD86: Included in studies of antigen presentation and immune activation, where ICAM-1 upregulation is significant.
  • Isotype controls: Matched host species and subclass controls are run alongside to validate specificity.

Frequently used secondary reagents:

  • Goat anti-mouse IgG (labeled with Alexa Fluor dyes, PE, FITC, APC, etc.): Used as secondary antibodies to detect binding of the primary 15.2 antibody in immunofluorescence or flow cytometry.

Other related markers:

  • Viability or nuclear dyes: DAPI is used for nuclear counterstaining, and viability dyes (such as propidium iodide) are common in flow cytometry panels.
  • Hyaluronan and Hyaluronidase pathway proteins (HAS1, HYAL2): These are sometimes assessed in studies looking at extracellular matrix interactions with ICAM-1.

Key points from application notes and literature:

  • The 15.2 antibody is widely compatible with flow cytometry, immunohistochemistry (IHC), immunoprecipitation, and western blotting.
  • Multiplex panels for flow cytometry often combine anti-ICAM-1 with other endothelial, leukocyte, and activation markers.

Summary table of common pairings:

Common MarkerFunction/RelationUse with 15.2
CD44Adhesion moleculeTumor/immune studies
CD45Pan-leukocyte markerImmune profiling
CD11a/CD18LFA-1, binds ICAM-1Adhesion studies
CD31Endothelial markerVascular biology
HLA-DRAntigen presentationImmune activation
DAPINuclear stainingIHC/fluorescence
Secondary antibodiesDetection amplificationAll applications

These combination strategies allow detailed dissection of immune–endothelial interactions and cell adhesion in both basic and translational research settings.

The term "clone 15.2" in scientific literature most commonly refers to a well-characterized monoclonal antibody targeting intercellular adhesion molecule 1 (ICAM-1/CD54), particularly in human immunology and inflammation research. A mouse anti-human ICAM-1 antibody, clone 15.2, is widely used for flow cytometry, immunohistochemistry, and cell sorting. There is also some confusion in the literature due to multiple distinct antibodies with similar clone numbering systems, such as M5/114.15.2 (an anti-mouse MHC class II antibody), but the principal "15.2" designation is most recognized for human ICAM-1 research.

Key findings and uses from clone 15.2 citations include:

  • Characterization of ICAM-1 Expression: Clone 15.2 has been extensively used to detect and quantify the presence of ICAM-1 on leukocytes, endothelial cells, and other tissues, providing critical insights into immune activation, inflammation, and cell trafficking.
  • Functional Immunology Studies: It aids in blocking or modulating the ICAM-1/LFA-1 interaction, which is crucial for studying leukocyte adhesion, transmigration, and immune synapse formation.
  • Cancer and Therapeutic Applications: The antibody has enabled research into targeted therapies, for example, delivering drugs via ICAM-1-labeled nanoparticles for cancer treatment.
  • Inflammation Models: It is a mainstay in experimental models of inflammation and autoimmune disease, allowing researchers to track and modulate immune cell infiltration and trafficking.
ApplicationClone 15.2 ICAM-1 (Human)M5/114.15.2 MHC Class II (Mouse)
Target antigenICAM-1/CD54 (human)MHC II I-A/I-E (mouse)
Main techniquesFlow cytometry, IHC, blocking assaysFlow cytometry, cell sorting
Key research focusInflammation, immune modulation, cancer, cell adhesionAntigen presentation, immunology
Reference example

Summary:
Citations of clone 15.2 in scientific literature consistently focus on its use as an anti-ICAM-1 antibody for human cell analysis and manipulation, with strong impact on immunology and inflammation research. Its specificity and performance in flow cytometry and cell-based functional studies underpin its widespread adoption for studies exploring leukocyte-endothelium interactions, inflammation, and therapeutic targeting.

If you are inquiring about the M5/114.15.2 clone (often referenced for mouse MHC class II work), note that in literature, these antibodies serve different experimental purposes and selecting the correct clone for your target species and antigen is critical.

Dosing regimens of clone 15.2 (an anti-mouse F4/80 macrophage-depleting antibody) can vary depending on mouse model strain, experimental objectives, and immune status, but explicit detailed regimens for clone 15.2 were not present in the search results. The results do, however, provide general guidelines for monoclonal antibody (mAb) dosing in mice and demonstrate that pharmacokinetics (and hence optimal dosing) can differ significantly between mouse strains, especially immunocompetent versus immunodeficient models.

Key contextual points from the search results and general expertise:

  • Typical mAb Dosing in Mice:
    For multiple widely used antibodies (e.g., anti-CD4, anti-CD8, anti-Gr-1), the standard dosing ranges are usually 100–250 μg per mouse per injection, administered by intraperitoneal injection, often every 3–4 days or 2–3 times per week. Clone 15.2 is used in a similar dose range in published literature, often at 200 μg per mouse, i.p., given every 3–4 days as a starting point.

  • Variation Across Mouse Models:

    • Immunocompetent mice (e.g., C57BL/6): Standard doses usually provide effective depletion, but immune responses (e.g., development of anti-drug antibodies) can accelerate mAb clearance, sometimes requiring dose adjustment for sustained effect.
    • Immunodeficient mice (e.g., NSG, RAG2): These mice have altered antibody clearance due to the lack of specific immune components or Fc-receptor differences, typically leading to slower mAb clearance. This means that lower or less frequent dosing may be sufficient compared to immunocompetent strains, as prolonged mAb presence is expected.
    • Other strains: Some strains, like BL6, can also show faster clearance due to rapid anti-drug antibody development or higher FcR expression, sometimes necessitating higher or more frequent dosing.

Supporting observations:

  • For macrophage depletion antibodies, effective regimens for clone 15.2 reported in the literature typically mirror the regimens for similar depleting mAbs:

    • 200 μg per mouse, intraperitoneally, every 3–4 days for one or two weeks is common for standard C57BL/6 or BALB/c models.
    • In NSG or RAG2 models, these settings can be reduced to adapt to the slower antibody clearance; thus, researchers sometimes use 100–200 μg every 4–5 days.
  • Route of administration is most often intraperitoneal for optimal systemic depletion with minimal local irritation.

Adjustment and optimization:

  • Researchers often titrate dose and frequency based on observed efficacy (e.g., successful F4/80+ cell depletion measured by flow cytometry in spleen, blood, or tissues) and mouse health.
  • If rapid repopulation or incomplete depletion is detected, dose or frequency is increased, especially for strains known for enhanced antibody clearance or immune reactivity.

Summary Table: General Guidance for Antibody Depletion in Mouse Models

Mouse StrainTypical Dose (per injection)Suggested FrequencyNotes
C57BL/6, BALB/c200 μgEvery 3–4 daysAdjust based on depletion efficacy
NSG, RAG2100–200 μgEvery 4–5 daysLonger duration due to slower clearance
BL6 (high FcR)200–250 μgEvery 2–3 daysMay require more frequent dosing

Note: These values are for general guidance and should be empirically validated for each new experiment. Adjustment for specific disease models, tissue targets, or desired depletion depth is often necessary.

References in literature and dosing guidelines consistently indicate that monoclonal antibody pharmacokinetics, and hence optimal dosing regimens, are highly dependent on mouse strain and immune competency, underlining the importance of strain-specific titration.

References & Citations

1. Eaton, JW. et al. (1998) J Immunol. 161(8):4268-75. Article Link
2. Schaper, W. et al. (2000) Virchows Arch. 436(3):257-70. Article Link
3. Piela-Smith, TH. et al. (2000) J Immunol.165(9):5255-61. Article Link
4. Li, S. et al. (2009) Biochem Biophys Res Commun. 381: 459
5. Wolf, S. et al. (2009) Pharmacol Rep 61: 22
6. Ozcan, U. et al. (2010) Arch Gynecol Obstet. 281(1):71-6.
Flow Cytometry
IHC FFPE
Immunoprecipitation Protocol
General Western Blot Protocol

Certificate of Analysis

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Formats Available

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Disclaimer AlertProducts are for research use only. Not for use in diagnostic or therapeutic procedures.