Product Description
Size: 100µL
Rabbit Polyclonal FRAS1 antibody. Suitable for IP, WB and reacts with Human samples. Cited in 3 publications. Immunogen corresponding to Synthetic Peptide within Human FRAS1 aa 3000-3100.
Key facts
Host species:Rabbit,
Clonality:Polyclonal,
Isotype:IgG,
Carrier free:No,
Reacts with:Human,
Applications:IP, WBSee reactivity dataSee the reactivity data table below for information on validated species and application combinations.,
Immunogen:Synthetic Peptide within Human FRAS1 aa 3000-3100. The exact immunogen used to generate this antibody is proprietary information.Q86XX4
Properties and Storage Information:
Form-Liquid, Purification technique-Affinity purification Immunogen, Purification notes-ab240583 was affinity purified using an epitope specific to FRAS1 immobilized on solid support., Storage buffer-pH: 6.8 - 7.4Preservative: 0.09% Sodium azideConstituents: Tris buffered saline, 0.1% 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-+4°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.
FRAS1 (Fraser syndrome 1) is a protein with a mass of approximately 419 kDa. It is expressed in the basement membrane zone of epithelial tissues particularly in the skin lungs kidneys and developing eyes. FRAS1 belongs to the extracellular matrix and plays a critical role in the structural organization of these tissues. This protein is also known as Fraser syndrome protein 1 and mutations in the FRAS1 gene can cause developmental defects.
Biological function summary
FRAS1 interacts with other extracellular matrix proteins to maintain the integrity of basement membranes. It forms a complex with FREM2 (Fras1 related extracellular matrix protein 2) and FREM1 (Fras1 related extracellular matrix protein 1). This complex is important for the adhesion between epithelial and mesenchymal cells during embryonic development ensuring proper organ formation and function. The correct assembly of this protein complex is essential for tissue integrity.
Pathways
FRAS1 participates in the assembly and organization of the extracellular matrix. It has an important role in epithelial-mesenchymal signaling particularly during embryonic development. This protein interacts with BMP4 (Bone Morphogenetic Protein 4) within these pathways influencing morphogenetic processes. FRAS1's participation in these pathways ensures proper organ structure and function by maintaining stable cellular environments.
FRAS1 is most notably associated with Fraser syndrome a genetic disorder characterized by cryptophthalmos syndactyly and renal agenesis. Mutations in the FRAS1 often resulting in a loss of function cause this syndrome. Another relevant condition is renal malformation which corresponds with disrupted FRAS1 function. Through these conditions FRAS1 also links to other proteins such as nephronectin that is involved in kidney development and maintenance.
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Collaboration
Tony Tang
Email: Tony.Tang@iright.com
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