FMR1 Antikörper (AA 36-279)

Produktnummer ABIN2721254

Der Maus Monoklonal anti-FMR1 Antikörper (Klon 1D10) (ABIN2721254) detektiert spezifisch FMR1 in WB und IHC. Dieser Antikörper reagiert spezifisch mit Proben aus Human, Maus, Ratte, Hund und Affe.

Kurzübersicht für FMR1 Antikörper (AA 36-279) (ABIN2721254)

Target: FMR1 (Fragile X Mental Retardation 1 (FMR1))

Reaktivität: Human, Maus, Ratte, Hund, Affe

Wirt: Maus

Klonalität: Monoklonal

Konjugat: Dieser FMR1 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB), Immunohistochemistry (IHC)

Klon: 1D10

Produktdetails anti-FMR1 Antikörper

Bindungsspezifität: AA 36-279

Produktmerkmale: Homo sapiens fragile X mental retardation 1 (FMR1), transcript variant ISO1

Aufreinigung: Purified from mouse ascites fluids by affinity chromatography

Immunogen: Human recombinant protein fragment corresponding to amino acids 36-279 of human FMR1(NP_002015) produced in E.coli.

Isotyp: IgG2b

Anwendungsinformationen

Applikationshinweise: WB 1:500~2000, IHC 1:50,

Kommentare:

The concentration of the product may vary between diferrent lots.

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: 0.5-1.0 mg/mL

Buffer: PBS (PH 7.3) containing 1 % BSA, 50 % glycerol and 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.

Lagerung: -20 °C

Details zu FMR1

Target: FMR1 (Fragile X Mental Retardation 1 (FMR1))

Andere Bezeichnung: FMR1

Hintergrund: The protein encoded by this gene binds RNA and is associated with polysomes. The encoded protein may be involved in mRNA trafficking from the nucleus to the cytoplasm. A trinucleotide repeat (CGG) in the 5' UTR is normally found at 6-53 copies, but an expansion to 55-230 repeats is the cause of fragile X syndrome. Expansion of the trinucleotide repeat may also cause one form of premature ovarian failure (POF1). Multiple alternatively spliced transcript variants that encode different protein isoforms and which are located in different cellular locations have been described for this gene.

Molekulargewicht: 71 kDa

Gen-ID: 2332

NCBI Accession: NM_002024

HGNC: 2332

Pathways: Regulation of Muscle Cell Differentiation, Skeletal Muscle Fiber Development