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

N° du produit ABIN2712880

Détail du produit

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

Type de proteíne: Recombinant

Attributs du protein: Transcript Variant 1

Origine: Humain

Source: HEK-293 Cells

Purification/Conjugué: Cette CLIP2 protéine est marqué à la Myc-DYKDDDDK Tag.

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

Attributs du produit:

• Recombinant human CLIP2 (transcript variant 1) protein expressed in HEK293 cells.
• Produced with end-sequenced ORF clone

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

Information d'application

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

Commentaires:

The tag is located at the C-terminal.

Restrictions: For Research Use only

Stockage

Concentration: 50 μg/mL

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

Stock: -80 °C

Stockage commentaire: 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.

Détail du antigène

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

Autre désignation: Clip2 (CLIP2 Produits)

Synonymes: 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

Sujet: 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.

Poids moléculaire: 115.6 kDa

NCBI Accession: NP_003379

Pathways: Dynamique des Microtubules