NDE1 Protein (NDE1) (Transcript Variant 2) (Myc-DYKDDDDK Tag)
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- Antigène Voir toutes NDE1 Protéines
- NDE1
- Type de proteíne
- Recombinant
- Attributs du protein
- Transcript Variant 2
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Origine
- Humain
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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
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- Recombinant human NDE1 (transcript variant 2) protein expressed in HEK293 cells.
- Produced with end-sequenced ORF clone
- Pureté
- > 80 % as determined by SDS-PAGE and Coomassie blue staining
- Top Product
- Discover our top product NDE1 Protéine
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- Indications d'application
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Recombinant human proteins can be used for:
Native antigens for optimized antibody production
Positive controls in ELISA and other antibody assays - Commentaires
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The tag is located at the C-terminal.
- Restrictions
- For Research Use only
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- 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.
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- 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_060138
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