NDE1 Protein (NDE1) (Transcript Variant 1) (Myc-DYKDDDDK Tag)

N° du produit ABIN2726913

Détail du produit

Antigène: NDE1

Type de proteíne: Recombinant

Attributs du protein: Transcript Variant 1

Origine: Humain

Source: HEK-293 Cells

Purification/Conjugué: Cette NDE1 protéine est marqué à la Myc-DYKDDDDK Tag.

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

Attributs du produit:

• Recombinant human NDE1 (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: NDE1

Autre désignation: Nde1 (NDE1 Produits)

Synonymes: 2810027M15Rik Protein, AU042936 Protein, AW822251 Protein, Nude Protein, mNudE Protein, HOM-TES-87 Protein, LIS4 Protein, NDE Protein, NUDE Protein, NUDE1 Protein, fb82g01 Protein, im:7141877 Protein, wu:fb82g01 Protein, zgc:114109 Protein, nudE neurodevelopment protein 1 Protein, Nde1 Protein, NDE1 Protein, nde1 Protein

Sujet: This gene encodes a member of the nuclear distribution E (NudE) family of proteins. The encoded protein is localized at the centrosome and interacts with other centrosome components as part of a multiprotein complex that regulates dynein function. This protein plays an essential role in microtubule organization, mitosis and neuronal migration. Mutations in this gene cause lissencephaly 4, a disorder characterized by lissencephaly, severe brain atrophy, microcephaly, and severe mental retardation. Alternative splicing results in multiple transcript variants.

Poids moléculaire: 37.5 kDa

NCBI Accession: NP_001137451