CLIP2 Protein (Transcript Variant 1) (Myc-DYKDDDDK Tag)

Produktnummer ABIN2712880

Produktdetails

Target: CLIP2 (CAP-GLY Domain Containing Linker Protein 2 (CLIP2))

Protein-Typ: Recombinant

Proteineigenschaft: Transcript Variant 1

Spezies: Human

Quelle: HEK-293 Cells

Aufreinigungstag / Konjugat: Dieses CLIP2 Protein ist gelabelt mit Myc-DYKDDDDK Tag.

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

Produktmerkmale:

• Recombinant human CLIP2 (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: CLIP2 (CAP-GLY Domain Containing Linker Protein 2 (CLIP2))

Andere Bezeichnung: Clip2 (CLIP2 Produkte)

Synonyme: CLIP Protein, CLIP-115 Protein, CYLN2 Protein, WBSCR3 Protein, WBSCR4 Protein, WSCR3 Protein, WSCR4 Protein, Cyln2 Protein, B230327O20 Protein, Clip1 Protein, mKIAA0291 Protein, wbscr4 Protein, CAP-Gly domain containing linker protein 2 Protein, CAP-GLY domain containing linker protein 2 Protein, CLIP2 Protein, Clip2 Protein, clip2 Protein

Hintergrund: The protein encoded by this gene belongs to the family of cytoplasmic linker proteins, which have been proposed to mediate the interaction between specific membranous organelles and microtubules. This protein was found to associate with both microtubules and an organelle called the dendritic lamellar body. This gene is hemizygously deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23. Alternative splicing of this gene generates 2 transcript variants.

Molekulargewicht: 115.6 kDa

NCBI Accession: NP_003379

Pathways: Microtubule Dynamics