Rubicon Protein (Transcript Variant 2) (Myc-DYKDDDDK Tag)
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- Antigène Voir toutes Rubicon (KIAA0226) Protéines
- Rubicon (KIAA0226) (KIAA0226)
- 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 Rubicon protéine est marqué à la Myc-DYKDDDDK Tag.
- Application
- Antibody Production (AbP), Standard (STD)
- Attributs du produit
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- Recombinant human KIAA0226 (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 KIAA0226 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
- Rubicon (KIAA0226) (KIAA0226)
- Autre désignation
- Kiaa0226 (KIAA0226 Produits)
- Synonymes
- RUBICON Protein, 5330403K09 Protein, Kiaa0226 Protein, Rubicon Protein, mKIAA0226 Protein, RUN and cysteine rich domain containing beclin 1 interacting protein Protein, KIAA0226 Protein, RUN domain and cysteine-rich domain containing, Beclin 1-interacting protein Protein, RUBCN Protein, KIAA0226 Protein, Rubcn Protein
- Sujet
- The protein encoded by this gene is a negative regulator of autophagy and endocytic trafficking and controls endosome maturation. This protein contains two conserved domains, an N-terminal RUN domain and a C-terminal DUF4206 domain. The RUN domain is involved in Ras-like GTPase signaling, and the DUF4206 domain contains a diacylglycerol (DAG) binding-like motif. Mutation in this gene results in deletion of the DAG binding-like motif and causes a recessive ataxia. Alternatively spliced transcript variants encoding distinct isoforms have been found for this gene.
- Poids moléculaire
- 108.4 kDa
- NCBI Accession
- NP_055502
- Pathways
- Autophagy
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