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Home >> Antibodies >> IBA1 Antibody / AIF-1

IBA1 Antibody / AIF-1 (R32736)

  Catalog No Formulation Size Price (USD)  
Image R32736 0.5mg/ml if reconstituted with 0.2ml sterile DI water 100 ug 449
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IHC analysis of IBA1/AIF-1 using anti-Iba1/AIF-1 antibody. IBA1/AIF-1 was detected in a paraffin-embedded section of mouse brain tissue. Heat-mediated antigen retrieval was performed in EDTA buffer (pH 8.0). The tissue section was blocked with 10% goat serum and incubated with rabbit anti-IBA1/AIF-1 antibody overnight at 4°C. Peroxidase-conjugated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using an HRP-conjugated detection system with DAB as the chromogen.
IHC analysis of IBA1/AIF-1 using anti-Iba1/AIF-1 antibody. IBA1/AIF-1 was detected in a paraffin-embedded section of mouse brain tissue. Heat-mediated antigen retrieval was performed in EDTA buffer (pH 8.0). The tissue section was blocked with 10% goat serum and incubated with rabbit anti-IBA1/AIF-1 antibody overnight at 4°C. Peroxidase-conjugated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using an HRP-conjugated detection system with DAB as the chromogen.
IHC analysis of IBA1/AIF-1 using anti-IBA1/AIF-1 antibody. IBA1/AIF-1 was detected in paraffin-embedded sections of rat brain tissue. Heat-mediated antigen retrieval was performed in EDTA buffer (pH 8.0). The tissue sections were blocked with 10% goat serum and incubated with rabbit anti-IBA1/AIF-1 antibody overnight at 4°C. Peroxidase-conjugated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue sections were developed using an HRP-conjugated detection system with DAB as the chromogen.
IHC analysis of IBA1/AIF-1 using anti-IBA1/AIF-1 antibody. IBA1/AIF-1 was detected in paraffin-embedded sections of rat brain tissue. Heat-mediated antigen retrieval was performed in EDTA buffer (pH 8.0). The tissue sections were blocked with 10% goat serum and incubated with rabbit anti-IBA1/AIF-1 antibody overnight at 4°C. Peroxidase-conjugated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue sections were developed using an HRP-conjugated detection system with DAB as the chromogen.
IHC analysis of IBA1/AIF-1 using anti-IBA1/AIF-1 antibody. IBA1/AIF-1 was detected in paraffin-embedded sections of pig brain tissue. Heat-mediated antigen retrieval was performed in EDTA buffer (pH 8.0). The tissue sections were blocked with 10% goat serum and incubated with rabbit anti-IBA1/AIF-1 antibody overnight at 4°C. Peroxidase-conjugated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue sections were developed using an HRP-conjugated detection system with DAB as the chromogen.
IHC analysis of IBA1/AIF-1 using anti-IBA1/AIF-1 antibody. IBA1/AIF-1 was detected in paraffin-embedded sections of human spleen tissue. Heat-mediated antigen retrieval was performed in EDTA buffer (pH 8.0). The tissue sections were blocked with 10% goat serum and incubated with rabbit anti-IBA1/AIF-1 antibody overnight at 4°C. Peroxidase-conjugated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue sections were developed using an HRP-conjugated detection system with DAB as the chromogen.
IHC analysis of IBA1/AIF-1 using anti-IBA1/AIF-1 antibody. IBA1/AIF-1 was detected in paraffin-embedded sections of human spleen tissue. Heat-mediated antigen retrieval was performed in EDTA buffer (pH 8.0). The tissue sections were blocked with 10% goat serum and incubated with rabbit anti-IBA1/AIF-1 antibody overnight at 4°C. Peroxidase-conjugated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue sections were developed using an HRP-conjugated detection system with DAB as the chromogen.
Western blot analysis of IBA1 Antibody / AIF-1. IBA1/AIF-1 antibody immunoreactivity is observed in human HEL and THP-1 whole cell lysates. Proteins were separated by SDS-PAGE under reducing conditions and transferred to a nitrocellulose membrane. Lane 1: human HEL whole cell lysates; Lane 2: human THP-1 whole cell lysates. A distinct band is detected at approximately 17 kDa, consistent with the predicted molecular weight of IBA1/AIF-1.
Availability 1-3 business days
Species Reactivity Human, Mouse, Rat, Pig
Format Antigen affinity purified
Host Rabbit
Clonality Polyclonal (rabbit origin)
Isotype Rabbit IgG
Purity Antigen affinity
Buffer Lyophilized from 1X PBS with 2% Trehalose
UniProt P55008
Localization Cytoplasmic, membranous
Applications Western Blot : 0.5-1ug/ml
Immunohistochemistry (FFPE) : 2-5ug/ml
Limitations This IBA1 antibody is available for research use only.
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Description

IBA1 antibody recognizes Ionized calcium-binding adapter molecule 1 (AIF-1), a small cytoplasmic protein predominantly expressed in cells of the myeloid lineage, most notably microglia in the central nervous system and macrophages in peripheral tissues. IBA1 is widely used as a cellular marker for microglial identification due to its consistent expression across resting and activated microglial states and its strong association with innate immune cell function and immune surveillance activity within neural tissue.

Ionized calcium-binding adapter molecule 1 is encoded by the AIF1 gene and produces a highly conserved protein containing EF-hand calcium-binding motifs. These structural elements enable calcium-dependent protein interactions that link intracellular signaling events to cytoskeletal remodeling. Through these interactions, IBA1 associates with actin-regulatory proteins and contributes to changes in cell shape, membrane ruffling, and cytoplasmic extension, all of which are critical for immune cell motility and phagocytic behavior.

Functionally, IBA1 plays an important role in regulating actin dynamics during microglial activation. Microglia rely on rapid cytoskeletal rearrangement to survey their microenvironment, migrate toward sites of injury or infection, and engulf cellular debris. IBA1 expression supports these processes by facilitating actin cross-linking and stabilizing membrane protrusions. These functions are essential for both homeostatic immune surveillance and reactive immune responses in the central nervous system.

Under physiological conditions, IBA1 is constitutively expressed in resting microglia, where it supports basal motility and continuous environmental sensing. Upon immune activation triggered by neuronal damage, infection, ischemia, or neurodegenerative processes, IBA1 expression is frequently upregulated. This increase correlates with well-characterized morphological changes, including retraction of fine cellular processes, enlargement of the cell body, and increased phagocytic capacity. These changes reflect a shift from a surveillant to an activated immune phenotype.

IBA1 is primarily localized to the cytoplasm, with enrichment near the plasma membrane and within actin-rich regions of the cell. In tissue sections, IBA1 immunoreactivity typically highlights microglial cell bodies and branching processes, providing clear visualization of microglial distribution and morphology. This staining pattern makes IBA1 antibody-based detection particularly useful for assessing microglial density, activation state, and spatial organization across different brain regions and experimental conditions.

Outside the central nervous system, IBA1 is expressed by macrophages and related myeloid cells in tissues such as spleen, lymph nodes, liver, and sites of inflammation. In these peripheral contexts, IBA1 contributes to immune cell migration, phagocytosis, and inflammatory signaling. Detection of IBA1-positive macrophages is commonly used to evaluate immune cell infiltration, tissue remodeling, and inflammatory status in both normal and pathological samples.

Altered microglial activation marked by changes in IBA1 expression has been implicated in a wide range of pathological conditions, including neurodegenerative diseases, traumatic brain injury, ischemic stroke, multiple sclerosis, and tumor-associated neuroinflammation. Because IBA1 expression reflects both microglial presence and activation-associated morphological changes, it is frequently used to assess immune involvement and disease progression in experimental models and translational research settings. NSJ Bioreagents provides reagents intended for research use to support studies of IBA1 expression in microglia and macrophage populations.

An IBA1 antibody is suitable for research applications requiring detection and visualization of microglia or macrophage populations, including studies focused on neuroinflammation, innate immune responses, immune cell dynamics, and tissue-resident myeloid cell biology.

Application Notes

Optimal dilution of the IBA1 antibody should be determined by the researcher.

Immunogen

Amino acids 99-133 (ETFSYPDFLRMMLGKRSAILKMILMYEEKAREKEK) from the human protein were used as the immunogen for the IBA1 antibody.

Storage

After reconstitution, the IBA1 antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.

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