Rabbit Polyclonal FREM1 antibody. Suitable for IHC-P and reacts with Human samples. Immunogen corresponding to Synthetic Peptide within Human FREM1 conjugated to Keyhole Limpet Haemocyanin.
pH: 7.4
Preservative: 0.02% Sodium azide
Constituents: 99% PBS
IHC-P | |
---|---|
Human | Tested |
Mouse | Predicted |
Species | Dilution info | Notes |
---|---|---|
Species Human | Dilution info 10 µg/mL | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Mouse | Dilution info - | Notes - |
Extracellular matrix protein that plays a role in epidermal differentiation and is required for epidermal adhesion during embryonic development.
C9orf143, C9orf145, C9orf154, FREM1, FRAS1-related extracellular matrix protein 1, Protein QBRICK
Rabbit Polyclonal FREM1 antibody. Suitable for IHC-P and reacts with Human samples. Immunogen corresponding to Synthetic Peptide within Human FREM1 conjugated to Keyhole Limpet Haemocyanin.
pH: 7.4
Preservative: 0.02% Sodium azide
Constituents: 99% PBS
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FREM1 also known as Fras1-related extracellular matrix protein 1 serves mechanical roles by interacting with the extracellular matrix. This protein has a mass of approximately 230 kDa. It is prominently expressed in skin kidney and lung tissues. FREM1's interactions contribute to the structural stability and organization of tissues aiding their resilience and function.
FREM1 plays a critical role in skin and organ development. It is an important part of the Fraser complex which is essential during the formation of epithelial and basement membranes. The protein's function supports cellular adhesion and proper tissue morphogenesis. These roles are necessary for maintaining tissue integrity making it well-integrated into developmental processes.
FREM1 integrates with developmental signaling cascades essential to epithelial integrity and tissue cohesion. Notably it participates in the Wnt signaling pathway which is fundamental for cell fate determination. Through these pathways FREM1 coordinates with other proteins like FRAS1 and FREM2 ensuring proper signaling and communication within cell environments.
FREM1 mutations and disruptions relate to Fraser syndrome which involves congenital malformations affecting the eyes ears and skin. FREM1's interaction with FRAS1 and FREM2 is critical in this context as these proteins form the Fraser complex. Additionally irregularities in FREM1 expression may relate to kidney dysplasia highlighting its role in normal organ morphogenesis and function.
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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.
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ab117566, at 10 µg/ml, staining FREM1 in formalin fixed, paraffin embedded Human tonsil tissue by Immunohistochemistry.
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