MFAP1 Antikörper (AA 83-437)

Produktnummer ABIN7876941

Der Kaninchen Polyklonal anti-MFAP1 Antikörper wird verwendet zum Nachweis von MFAP1 in Proben von Human und Maus. Er wurde validiert für WB, ELISA, FACS und IF.

Kurzübersicht für MFAP1 Antikörper (AA 83-437) (ABIN7876941)

Target: MFAP1 (Microfibrillar Associated Protein 1 (MFAP1))

Reaktivität: Human, Maus

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser MFAP1 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB), ELISA, Flow Cytometry (FACS), Immunofluorescence (IF)

Produktdetails anti-MFAP1 Antikörper

Bindungsspezifität: AA 83-437

Verwendungszweck: MFAP1 Antibody / Microfibrillar-associated protein 1

Aufreinigung: Antigen affinity purified

Immunogen: An E.coli-derived human recombinant protein (D83-K437) was used as the immunogen for the MFAP1 antibody.

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: Optimal dilution of the MFAP1 antibody should be determined by the researcher.

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Lyophilized

Buffer: 0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

Lagerung: 4 °C,-20 °C

Informationen zur Lagerung: After reconstitution, the MFAP1 antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.

Details zu MFAP1

Target: MFAP1 (Microfibrillar Associated Protein 1 (MFAP1))

Andere Bezeichnung: MFAP1

Hintergrund: Microfibrillar-associated protein 1 is a protein that in humans is encoded by the MFAP1 gene. Microfibrils are an important component of the extracellular matrix of many tissues and can either associate with or without elastin. Several microfibril associated proteins (MFAPs) have been cloned, including MFAP1, MFAP3 and MFAP4. The MFAP1 and MFAP3 genes are localized near the fibrillin genes FBN1 and FBN2, respectively. Mutations in FBN1 are linked to Marfan syndrome. Mutations in FBN2 have been linked to congenital contractural arachnodactyly. This suggests roles for MFAP1 and MFAP3 in heritable diseases affecting microfibrils. Deletion of MFAP4 was found in 30 of 31 patients with Smith-Magenis syndrome (SMS), a clinically recognizable multiple congenital anomaly/mental retardation syndrome

UniProt: P55081