LZTFL1 Protein (Myc-DYKDDDDK Tag)
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- Antigène Voir toutes LZTFL1 Protéines
- LZTFL1 (Leucine Zipper Transcription Factor-Like 1 (LZTFL1))
- Type de proteíne
- Recombinant
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Origine
- Humain
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Source
- HEK-293 Cells
- Purification/Conjugué
- Cette LZTFL1 protéine est marqué à la Myc-DYKDDDDK Tag.
- Application
- Antibody Production (AbP), Standard (STD)
- Attributs du produit
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- Recombinant human LZTFL1 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 LZTFL1 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
- LZTFL1 (Leucine Zipper Transcription Factor-Like 1 (LZTFL1))
- Autre désignation
- Lztfl1 (LZTFL1 Produits)
- Synonymes
- lztfl1 Protein, MGC53120 Protein, LZTFL1 Protein, DKFZp469B0113 Protein, fb53f12 Protein, wu:fb53f12 Protein, zgc:56268 Protein, BBS17 Protein, 5530402H04Rik Protein, 6130400H19Rik Protein, AI414725 Protein, AW048545 Protein, leucine zipper transcription factor like 1 L homeolog Protein, leucine zipper transcription factor like 1 Protein, leucine zipper transcription factor-like 1 Protein, lztfl1.L Protein, LZTFL1 Protein, lztfl1 Protein, Lztfl1 Protein
- Sujet
- This gene encodes a ubiquitously expressed protein that localizes to the cytoplasm. This protein interacts with Bardet-Biedl Syndrome (BBS) proteins and, through its interaction with BBS protein complexes, regulates protein trafficking to the ciliary membrane. Nonsense mutations in this gene cause a form of Bardet-Biedl Syndrome a ciliopathy characterized in part by polydactyly, obesity, cognitive impairment, hypogonadism, and kidney failure. This gene may also function as a tumor suppressor possibly by interacting with E-cadherin and the actin cytoskeleton and thereby regulating the transition of epithelial cells to mesenchymal cells. Alternative splicing of this gene results in multiple transcript variants.
- Poids moléculaire
- 34.4 kDa
- NCBI Accession
- NP_065080
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