FREM1 anticorps (C-Term)

N° du produit ABIN783634

Cet anticorps Lapin Polyclonal détecte spécifiquement FREM1 dans WB, IF et EIA. Il présente une réactivité envers Humain et Souris.

Aperçu rapide pour FREM1 anticorps (C-Term) (ABIN783634)

Antigène: FREM1 (FRAS1 Related Extracellular Matrix 1 (FREM1))

Reactivité: Humain, Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp FREM1 est non-conjugé

Application: Western Blotting (WB), Immunofluorescence (IF), Enzyme Immunoassay (EIA)

Détail du produit anti-FREM1 anticorps

Épitope: C-Term

Specificité: This antibody rescts with Muman and Mouse FREM1 and is predicted to not cross-react with other FRAS members.

Purification: Affinity Chromatography purified via peptide column

Immunogène: 15 amino acid peptide near the carboxy terminus of Human FREM1

Information d'application

Indications d'application: Optimal working dilution should be determined by the investigator.

Restrictions: For Research Use only

Stockage

Concentration: 1.0 mg/mL

Buffer: PBS, 0.02 % Sodium Azide

Agent conservateur: Sodium azide

Précaution d'utilisation: This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Conseil sur la manipulation: Avoid repeated freezing and thawing.

Stock: 4 °C/-20 °C

Stockage commentaire: Store undiluted at 2-8 °C for one month or (in aliquots) at -20 °C for longer.

Détails sur FREM1

Antigène: FREM1 (FRAS1 Related Extracellular Matrix 1 (FREM1))

Autre désignation: FREM1

Sujet: FREM1 is a member of the FRAS1-related extracellular matrix protein family and is thought to play a role in craniofacial and renal development. FREM1 functions as an extracellular matrix protein that is essential for epidermal adhesion during embryogenesis and may also participate in epidermal differentiation. It is recognized by cells in the embryonic skin and hair follicles through different members of the integrin family. Deficiency in the Fras1/Frem genes gives rise to the bleb phenotype, which is equivalent to the human hereditary disorder Fraser syndrome.Synonyms: C9orf143, C9orf145, C9orf154, FRAS1-related extracellular matrix protein 1, Protein QBRICK

ID gène: 158326

NCBI Accession: NP_001171175

UniProt: Q5H8C1