TOM1L2 Protein (Transcript Variant 3) (Myc-DYKDDDDK Tag)
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- Target Alle TOM1L2 Proteine anzeigen
- TOM1L2 (Target of Myb1-Like 2 (TOM1L2))
- Protein-Typ
- Recombinant
- Proteineigenschaft
- Transcript Variant 3
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Spezies
- Human
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Quelle
- HEK-293 Cells
- Aufreinigungstag / Konjugat
- Dieses TOM1L2 Protein ist gelabelt mit Myc-DYKDDDDK Tag.
- Applikation
- Antibody Production (AbP), Standard (STD)
- Produktmerkmale
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- Recombinant human TOM1L2 (transcript variant 3) protein expressed in HEK293 cells.
- Produced with end-sequenced ORF clone
- Reinheit
- > 80 % as determined by SDS-PAGE and Coomassie blue staining
- Top Product
- Discover our top product TOM1L2 Protein
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- Applikationshinweise
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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 - Kommentare
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The tag is located at the C-terminal.
- Beschränkungen
- Nur für Forschungszwecke einsetzbar
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- Konzentration
- 50 μg/mL
- Buffer
- 25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10 % glycerol.
- Lagerung
- -80 °C
- Informationen zur Lagerung
- 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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- Target
- TOM1L2 (Target of Myb1-Like 2 (TOM1L2))
- Andere Bezeichnung
- Tom1l2 (TOM1L2 Produkte)
- Synonyme
- 2900016I08Rik Protein, A730055F12Rik Protein, AU042072 Protein, Srebf1 Protein, target of myb1 like 2 membrane trafficking protein Protein, target of myb1 like 2 membrane trafficking protein L homeolog Protein, target of myb1-like 2 (chicken) Protein, TOM1L2 Protein, tom1l2.L Protein, Tom1l2 Protein
- Hintergrund
- This gene belongs to a small gene family whose members have an N-terminal VHS domain followed by a GAT domain domains which typically participate in vesicular trafficking. The canonical protein encoded by this gene also has a C-terminal clathrin binding motif. This protein has been shown to interact with Tollip, clathrin and ubiquitin and is thought to play a role in endosomal sorting. This gene resides in the 3.7 Mb deletion of chromosome region 17p11.2 that is associated with Smith-Magenis syndrome. Alternative splicing results in multiple transcript variants encoding distinct proteins.
- Molekulargewicht
- 55.4 kDa
- NCBI Accession
- NP_001076437
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