MID1 Protein (Transcript Variant 1) (Myc-DYKDDDDK Tag)

Produktnummer ABIN2726004

Produktdetails

Target: MID1 (Midline 1 (MID1))

Protein-Typ: Recombinant

Proteineigenschaft: Transcript Variant 1

Spezies: Human

Quelle: HEK-293 Cells

Aufreinigungstag / Konjugat: Dieses MID1 Protein ist gelabelt mit Myc-DYKDDDDK Tag.

Applikation: Antibody Production (AbP), Standard (STD)

Produktmerkmale:

• Recombinant human Midline-1 (transcript variant 1) protein expressed in HEK293 cells.
• Produced with end-sequenced ORF clone

Reinheit: > 80 % as determined by SDS-PAGE and Coomassie blue staining

Anwendungsinformationen

Applikationshinweise: Recombinant human proteins can be used for:
Native antigens for optimized antibody production
Positive controls in ELISA and other antibody assays

Kommentare:

The tag is located at the C-terminal.

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Konzentration: 50 μg/mL

Buffer: 25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10 % glycerol.

Lagerung: -80 °C

Informationen zur Lagerung: Store at -80°C. Thaw on ice, aliquot to individual single-use tubes, and then re-freeze immediately. Only 2-3 freeze thaw cycles are recommended.

Antigendetails

Target: MID1 (Midline 1 (MID1))

Andere Bezeichnung: Midline-1 (MID1 Produkte)

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

Hintergrund: The protein encoded by this gene is a member of the tripartite motif (TRIM) family, also known as the &aposRING-B box-coiled coil&apos (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: 75.1 kDa

NCBI Accession: NP_000372