MID1 Antikörper

Produktnummer ABIN6571035

Produktdetails anti-MID1 Antikörper

Target: MID1 (Midline 1 (MID1))

Reaktivität: Human, Maus

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser MID1 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB), Immunofluorescence (IF)

Aufreinigung: Affinity purification

Immunogen: Recombinant fusion protein of human MID1 (NP_000372.1).

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: WB 1:500-1:2000 IF 1:50-1:100

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: 1 mg/mL

Buffer: PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3

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

Informationen zur Lagerung: Store at -20°C. Avoid freeze / thaw cycles.

Details zu MID1

Target: MID1 (Midline 1 (MID1))

Andere Bezeichnung: MID1 (MID1 Produkte)

Synonyme: BBBG1 antikoerper, FXY antikoerper, GBBB1 antikoerper, MIDIN antikoerper, OGS1 antikoerper, OS antikoerper, OSX antikoerper, RNF59 antikoerper, TRIM18 antikoerper, XPRF antikoerper, ZNFXY antikoerper, 61B3-R antikoerper, DXHXS1141 antikoerper, Fxy antikoerper, Trim18 antikoerper, Midline1 antikoerper, bbbg1 antikoerper, fxy antikoerper, gbbb1 antikoerper, midin antikoerper, ogs1 antikoerper, osx antikoerper, rnf59 antikoerper, trim18 antikoerper, xprf antikoerper, znfxy antikoerper, midline 1 antikoerper, midline 1 L homeolog antikoerper, MID1 antikoerper, Mid1 antikoerper, mid1 antikoerper, mid1.L antikoerper

Hintergrund: The protein encoded by this gene is a member of the tripartite motif (TRIM) family, also known as the 'RING-B box-coiled coil' (RBCC) subgroup of RING finger proteins. The TRIM motif includes three zinc-binding domains, a RING, a B-box type 1 and a B-box type 2, and a coiled-coil region. This protein forms homodimers which associate with microtubules in the cytoplasm. The protein is likely involved in the formation of multiprotein structures acting as anchor points to microtubules. Mutations in this gene have been associated with the X-linked form of Opitz syndrome, which is characterized by midline abnormalities such as cleft lip, laryngeal cleft, heart defects, hypospadias, and agenesis of the corpus callosum. This gene was also the first example of a gene subject to X inactivation in human while escaping it in mouse. Alternative promoter use, alternative splicing and alternative polyadenylation result in multiple transcript variants that have different tissue specificities.

Molekulargewicht:

Observed_MW: 85kDa

Calculated_MW: 62kDa/75kDa

Gen-ID: 4281

UniProt: O15344