FREM1 Antikörper (C-Term)

Produktnummer ABIN783634

Dieses Kaninchen Polyklonal-Antikörper erkennt spezifisch FREM1 in WB, IF und EIA. Er zeigt eine Reaktivität gegenüber Human und Maus.

Kurzübersicht für FREM1 Antikörper (C-Term) (ABIN783634)

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

Reaktivität: Human, Maus

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser FREM1 Antikörper ist unkonjugiert

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

Produktdetails anti-FREM1 Antikörper

Bindungsspezifität: C-Term

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

Aufreinigung: Affinity Chromatography purified via peptide column

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

Anwendungsinformationen

Applikationshinweise: Optimal working dilution should be determined by the investigator.

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Konzentration: 1.0 mg/mL

Buffer: PBS, 0.02 % Sodium Azide

Konservierungsmittel: Sodium azide

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

Handhabung: Avoid repeated freezing and thawing.

Lagerung: 4 °C/-20 °C

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

Details zu FREM1

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

Andere Bezeichnung: FREM1

Hintergrund: 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

Gen-ID: 158326

NCBI Accession: NP_001171175

UniProt: Q5H8C1