Abcam, ab235445, Anti-FoxJ1 antibody [EPR21874]

Size: 100µL / 1mL
Anti-FoxJ1 antibody [EPR21874] (ab235445) is a rabbit monoclonal antibody detecting FoxJ1 in IHC-P . Suitable for Human, Mouse, Rat . - Biophysical QC for unrivalled batch-batch consistency - Over 10 publications
Key facts
Host species:Rabbit,
Clonality:Monoclonal,
Clone number:EPR21874,
Isotype:IgG,
Carrier free:No,
Reacts with:Mouse, Rat, Human,
Applications:IHC-PSee reactivity dataSee the reactivity data table below for information on validated species and application combinations.,
Immunogen:The exact immunogen used to generate this antibody is proprietary information.

Product details:
What is this antibody validated in?
Anti-FoxJ1 antibody [EPR21874] (ab235445) is a rabbit recombinant monoclonal antibody and is validated for use in Immunohistochemistry (IHC-P) in Human, Mouse, Rat samples.
Trusted by the scientific community
Anti-FoxJ1 [EPR21874] (ab235445) was first used in a scientific publication in 2018 and has been cited over 10 times in peer-reviewed journals.
Trial sizes available!
Test your antibody or perform pre-screening before committing to a larger quantity. Sold in 10µl.
Discover our selection of trial-size antibodies
Other related products
We have a range of other formats of antibody clone [EPR21874] also available for your convenience: ab235445, Carrier free -
ab238168
Patented technology
Our RabMAb
technology is a patented hybridoma-based technology for making rabbit monoclonal antibodies. For details on our patents, please refer to
RabMAb® patents
What are the advantages of a recombinant monoclonal antibody?
This product is a recombinant monoclonal antibody, which offers several advantages including:
- High batch-to-batch consistency and reproducibility
- Improved sensitivity and specificity
- Long-term security of supply
- Animal-free batch production
For more information, read more on
recombinant antibodies

Properties and Storage Information:
Form-Liquid, Purification technique-Affinity purification Protein A, Storage buffer-pH: 7.2 - 7.4Preservative: 0.01% Sodium azideConstituents: PBS, 40% Glycerol (glycerin, glycerine), 0.05% BSA, Shipped at conditions-Blue Ice, Appropriate short-term storage duration-1-2 weeks, Appropriate short-term storage conditions-+4°C, Appropriate long-term storage conditions--20°C, Aliquoting information-Upon delivery aliquot, Storage information-Avoid freeze / thaw cycle

Supplementary Information:
This supplementary information is collated from multiple sources and compiled automatically.
FoxJ1 also known as Forkhead Box J1 is a transcription factor that plays an important role in the regulation of gene expression. It is part of the forkhead family of transcription factors and has a molecular mass of approximately 44 kDa. FoxJ1 is expressed mainly in tissues with motile cilia such as the brain respiratory tract and reproductive organs. This expression pattern highlights its significance in tissues where ciliary movement is important for normal function.
Biological function summary
FoxJ1 is important in ciliogenesis the process of building cilia on the surface of cells. It acts as a master regulator by activating genes that code for ciliary components. This includes genes involved in the formation of the axoneme the core structure of cilia. FoxJ1 does not work alone; it functions within a network of other transcription factors and proteins to achieve effective cilia formation and movement. By controlling this process FoxJ1 ensures that ciliary structures develop and function correctly which is necessary for cellular motility and fluid movement across epithelial surfaces.
Pathways
FoxJ1 operates within critical pathways involved in cilia development and function. It integrates into the Wnt signaling pathway which is critical for embryogenesis and cell polarity. Additionally FoxJ1 interacts with the Notch signaling pathway. In these pathways it can relate to other transcription factors like Rfx3 which also influence cilia-related gene expression. FoxJ1 coordinates with these pathways to ensure precise regulation of cilia biogenesis and maintenance contributing to cellular processes that depend on functional cilia.
Deficient or malfunctioning FoxJ1 can lead to primary ciliary dyskinesia (PCD) and respiratory diseases. PCD results from impaired ciliary movement affecting respiratory tract function and fertility. Dysfunctional FoxJ1 expression can disrupt ciliary architecture connecting it to other proteins like DNAI1 which is often implicated in PCD. Abnormal FoxJ1 activity has also been linked to hydrocephalus where cerebrospinal fluid imbalances occur due to faulty cilia movement. In these conditions understanding FoxJ1's role provides insight into potential targets for therapeutic interventions.