FRG2B Antikörper (FITC)

Produktnummer ABIN1403366

Der Kaninchen Polyklonal Anti-FRG2B-Antikörper wurde für WB und IF (p) validiert. Er ist geeignet, FRG2B in Proben von Human zu detektieren.

Kurzübersicht für FRG2B Antikörper (FITC) (ABIN1403366)

Target: FRG2B (FSHD Region Gene 2 Family, Member B (FRG2B))

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser FRG2B Antikörper ist konjugiert mit FITC

Applikation: Western Blotting (WB), Immunofluorescence (Paraffin-embedded Sections) (IF (p))

Produktdetails anti-FRG2B Antikörper (FITC)

Kreuzreaktivität: Human

Aufreinigung: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human FRG2B

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: IF(IHC-P) 1:50-200

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: 1 μg/μL

Buffer: Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.

Konservierungsmittel: ProClin

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

Lagerung: -20 °C

Informationen zur Lagerung: Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

Haltbarkeit: 12 months

Details zu FRG2B

Target: FRG2B (FSHD Region Gene 2 Family, Member B (FRG2B))

Andere Bezeichnung: FRG2B

Hintergrund:

Synonyms: FRG2A, FRG2B, FRG2C, FRG2B_HUMAN, FSHD region gene 2 protein family member B, HSA10-FRG2, Protein FRG2-like-1.

Background: Chromosome 3 is made up of about 214 million bases encoding over 1,100 genes. Notably, there is a chemokine receptor gene cluster and a variety of human cancer related loci on chromosome 3. Particular regions of the chromosome 3 short arm are deleted in many types of cancer cells. Key tumor suppressing genes on chromosome 3 encode apoptosis mediator RASSF1, cell migration regulator HYAL1 and angiogenesis suppressor SEMA3B. Marfan Syndrome, porphyria, von Hippel-Lindau syndrome, osteogenesis imperfecta and Charcot-Marie-Tooth Disease are a few of the numerous genetic diseases associated with chromosome 3.

Gen-ID: 441581