Anti-Iba1 antibody is a goat polyclonal antibody that is used to detect Iba1 in IHC-P, Western blot. Suitable for Human, Rat samples.
- Cited in over 1350 publications
- Tried and trusted by researchers since 2003
pH: 7.3
Preservative: 0.02% Sodium azide
Constituents: Tris buffered saline, 0.5% BSA
IHC-P | WB | |
---|---|---|
Human | Tested | Tested |
Rat | Not recommended | Tested |
Macaque monkey | Not recommended | Predicted |
Pig | Not recommended | Predicted |
Species | Dilution info | Notes |
---|---|---|
Species Human | Dilution info 5 µg/mL | Notes Although we received several excellent papers on ab5076 working with rat IHC-P, rat is not a batch tested species for IHC-P and we cannot guarantee. Perform heat-mediated antigen retrieval with citrate buffer pH 6 before commencing with IHC staining protocol. |
Species | Dilution info | Notes |
---|---|---|
Species Rat | Dilution info - | Notes Although we received several excellent papers on ab5076 working with rat IHC-P, rat is not a batch tested species for IHC-P and we cannot guarantee. |
Species Pig | Dilution info - | Notes - |
Species Macaque monkey | Dilution info - | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Rat | Dilution info 1-3 µg/mL | Notes A 1 hour primary incubation is recommended for this product. We received several excellent Abreviews on this antibody working with mouse, however, mouse is not a batch tested species and we cannot guarantee that this antibody will work on mouse. Some of our customers have observed high background in mouse samples. We recommend blocking in milk (3% milk in TBST) for 1 hour at room temperature. Blocking with BSA gives high background. |
Species Human | Dilution info 1-3 µg/mL | Notes A 1 hour primary incubation is recommended for this product. We received several excellent Abreviews on this antibody working with mouse, however, mouse is not a batch tested species and we cannot guarantee that this antibody will work on mouse. Some of our customers have observed high background in mouse samples. We recommend blocking in milk (3% milk in TBST) for 1 hour at room temperature. Blocking with BSA gives high background. |
Species | Dilution info | Notes |
---|---|---|
Species Pig, Macaque monkey | Dilution info - | Notes - |
Select an associated product type
Actin-binding protein that enhances membrane ruffling and RAC activation. Enhances the actin-bundling activity of LCP1. Binds calcium. Plays a role in RAC signaling and in phagocytosis. May play a role in macrophage activation and function. Promotes the proliferation of vascular smooth muscle cells and of T-lymphocytes. Enhances lymphocyte migration. Plays a role in vascular inflammation.
Aif1
G1, IBA1, AIF1, Allograft inflammatory factor 1, AIF-1, Ionized calcium-binding adapter molecule 1, Protein G1
Anti-Iba1 antibody is a goat polyclonal antibody that is used to detect Iba1 in IHC-P, Western blot. Suitable for Human, Rat samples.
- Cited in over 1350 publications
- Tried and trusted by researchers since 2003
pH: 7.3
Preservative: 0.02% Sodium azide
Constituents: Tris buffered saline, 0.5% BSA
ab5076 is expected to recognize the isoforms represented by NP_001614 and NP_116573 but not NP_004838.
Although we received several excellent papers on ab5076 working with rat IHC-P, rat is not a batch tested species for IHC-P and we cannot guarantee.
Purified from goat serum by ammonium sulphate precipitation followed by antigen affinity chromatography using the immunizing peptide.
Find all reagents to label astrocytes in our "Microglia markers guide".
Anti-Iba1 antibody (ab5076) is a Goat Polyclonal antibody and is validated for use in IHC-P, WB in human, mouse, rat samples.
Anti-Iba1 antibody (ab5076) has been cited over 1354 times in peer reviewed journals and is trusted by the scientific community.
Abcams high quality validation processes ensure Anti-Iba1 antibody (ab5076) has high sensitivity and specificity.
Anti-Iba1 antibody (ab5076) has 100 independent reviews from customers.
Anti-Iba1 antibody (ab5076) specifically detects Iba1 (UniProt ID: P55008; Molecular weight: 17kDa) and is sold in 100 ug selling sizes.
Iba1 (Ionized calcium-binding adapter molecule 1; allograft inflammatory factor 1, AIF1) is a prominent microglial marker extensively used in neuroscience research. Its expression increases in various neurodegenerative conditions, including Alzheimer's disease (AD), indicating microglial activation and neuroinflammation. Researchers utilize Iba1 in stainings to assess microglial response and activity in different models, making it essential for understanding inflammatory processes in the brain. Changes in Iba1 expression provide valuable insights into neuroinflammation, highlighting its importance in studying diseases like AD.
The Iba1 antibody (ab5076) is commonly used as a marker of microglia activation in staining and immunohistochemistry, given that ionized calcium binding adaptor molecule 1 (Iba1) is a microglia/macrophage-specific calcium-binding protein with actin-bundling activity that participates in membrane ruffling and phagocytosis in activated microglia.
Iba1 also known as allograft inflammatory factor 1 (AIF1) is a protein with a molecular weight of approximately 17 kDa. It is widely expressed in microglia which are the resident immune cells of the central nervous system (CNS). Iba1 plays a mechanical role in actin-binding and modulating cytoskeleton dynamics which affects cell shape and motility. It is also found in other myeloid-derived cells including macrophages and monocytes where it influences cellular processes linked to inflammation and immune responses.
The involvement of Iba1 in actin polymerization impacts microglia's ability to perform phagocytosis and cytokine production. Iba1 does not appear to be part of any large protein complex but interacts directly with actin filaments to facilitate cytoskeletal reorganization. This function enables the cells to move and respond efficiently to tissue damage or pathogens in the CNS. It plays an important role in supporting cellular changes associated with immune surveillance and neuroinflammatory responses.
Microglial activation relies heavily on Iba1 for executing acts linked with neuroinflammation. Iba1 engages in the NF-kB signaling pathway significant in managing inflammatory responses. It interacts with proteins such as MyD88 and IRAK4 which aid in transmitting signals from toll-like receptors. These pathways enable changes in gene expression critical for microglial response to various stimuli. Furthermore Iba1 also contributes to the PI3K/Akt pathway where it influences cell survival and proliferation interacting with proteins like Akt1 and PTEN.
Iba1 has implications in neurodegenerative diseases notably Alzheimer's disease and multiple sclerosis. In Alzheimer's disease increased expression of Iba1 is observed in activated microglia around amyloid plaques suggesting a role in plaque clearance and neuroinflammation. The protein relates to amyloid precursor protein (APP) as microglia respond to abnormal accumulations. In multiple sclerosis Iba1 expression marks activated microglia involved in demyelination processes where it associates with proteins like myelin basic protein (MBP) highlighting its role in the disease's pathology.
We have tested this species and application combination and it works. It is covered by our product promise.
We have not tested this specific species and application combination in-house, but expect it will work. It is covered by our product promise.
This species and application combination has not been tested, but we predict it will work based on strong homology. However, this combination is not covered by our product promise.
We do not recommend this combination. It is not covered by our product promise.
We are dedicated to supporting your work with high quality reagents and we are here for you every step of the way should you need us.
In the unlikely event of one of our products not working as expected, you are covered by our product promise.
Full details and terms and conditions can be found here:
Terms & Conditions.
Iba1 immunohistochemistry staining of human spleen using goat anti-Iba1 antibody
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) analysis of human spleen tissue labelling Iba1 with ab5076 at 8µg/ml.
Heat induced antigen retrieval with citrate buffer Ph 6 HRP-staining.
Detected by chemiluminescence.
All lanes: Western blot - Anti-Iba1 antibody (ab5076) at 1 µg/mL
Lane 1: Human lymph node tissue lysate in RIPA buffer at 35 µg
Lane 2: Rat brain tissue lysate in RIPA buffer at 35 µg
Developed using the ECL technique.
Predicted band size: 16 kDa
Immunohistochemical analysis of formalin-fixed, paraffin-embedded human lateral prefrontal cortex tissue labeling iba1 labeled microglia (labeled with black arrows) within the cortex using ab5076 at 1/1000 dilution. (Cropped image).
Sections were rinsed in 0.01 m PBS, pH 7.4, followed by 10% serum matching the species of the secondary antibody, 5% bovine serum albumin, and 0.1% Triton X-100 in 0.01 m PBS blocking solution for 1 h and incubated for 2 days at 4 °C in primary antibody. The sections were rinsed in PBS and incubated overnight at 4 °C with a horse anti-Goat IgG (Biotinylated) secondary antibody.
Iba1 immunohistochemistry staining of human spleen using goat anti-Iba1 antibody
Negative control: Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) analysis of human spleen tissue labelling Iba1 with no primary antibody.
Heat induced antigen retrieval with citrate buffer Ph 6 HRP-staining.
Please note: All products are 'FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC OR THERAPEUTIC PROCEDURES'.
For licensing inquiries, please contact partnerships@abcam.com