TM4SF20 Protein (Myc-DYKDDDDK Tag)
TM4SF20
Origin: Human
Host: HEK-293 Cells
Recombinant
> 80 % as determined by SDS-PAGE and Coomassie blue staining
AbP, STD
1 image
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- Target See all TM4SF20 products
- TM4SF20 (Transmembrane 4 L Six Family Member 20 (TM4SF20))
- Protein Type
- Recombinant
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Origin
- Human
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Source
- HEK-293 Cells
- Purification tag / Conjugate
- This TM4SF20 protein is labelled with Myc-DYKDDDDK Tag.
- Application
- Antibody Production (AbP), Standard (STD)
- Characteristics
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- Recombinant human TM4SF20 protein expressed in HEK293 cells.
- Produced with end-sequenced ORF clone
- Purity
- > 80 % as determined by SDS-PAGE and Coomassie blue staining
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- Application Notes
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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 - Comment
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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.
- Storage
- -80 °C
- Storage Comment
- 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
- TM4SF20 (Transmembrane 4 L Six Family Member 20 (TM4SF20))
- Alternative Name
- Tm4sf20 (TM4SF20 Products)
- Synonyms
- pro994 Protein, tcce518 Protein, PRO994 Protein, TCCE518 Protein, 1810018L02Rik Protein, transmembrane 4 L six family member 20 Protein, transmembrane 4 L six family member 20 L homeolog Protein, TM4SF20 Protein, Tm4sf20 Protein, tm4sf20.L Protein, tm4sf20 Protein
- Background
- The protein encoded by this gene is a member of the four-transmembrane L6 superfamily. Members of this family function in various cellular processes including cell proliferation, motility, and adhesion via their interactions with integrins. In human brain tissue, this gene is expressed at high levels in the parietal lobe, occipital lobe, hippocampus, pons, white matter, corpus callosum, and cerebellum. Knockout of the homologous gene in mouse results in a neurobehavioral phenotype with suggested enhanced motor coordination. A deletion mutation in the human gene is associated with specific language impairment-5.
- Molecular Weight
- 24.9 kDa
- NCBI Accession
- NP_079071
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