ZFYVE27 Protein (Transcript Variant 2) (Myc-DYKDDDDK Tag)
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- Target See all ZFYVE27 Proteins
- ZFYVE27 (Zinc Finger, FYVE Domain Containing 27 (ZFYVE27))
- Protein Type
- Recombinant
- Protein Characteristics
- Transcript Variant 2
- Origin
- Human
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Source
- HEK-293 Cells
- Purification tag / Conjugate
- This ZFYVE27 protein is labelled with Myc-DYKDDDDK Tag.
- Application
- Antibody Production (AbP), Standard (STD)
- Characteristics
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- Recombinant human ZFYVE27 (transcript variant 2) protein expressed in HEK293 cells.
- Produced with end-sequenced ORF clone
- Purity
- > 80 % as determined by SDS-PAGE and Coomassie blue staining
- Top Product
- Discover our top product ZFYVE27 Protein
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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
- ZFYVE27 (Zinc Finger, FYVE Domain Containing 27 (ZFYVE27))
- Alternative Name
- Zfyve27 (ZFYVE27 Products)
- Synonyms
- ZFYVE27 Protein, MGC130947 Protein, spg33 Protein, im:7137347 Protein, zgc:153156 Protein, PROTRUDIN Protein, RP11-459F3.2 Protein, SPG33 Protein, 2210011N02Rik Protein, 9530077C24Rik Protein, AI426636 Protein, AI593546 Protein, AI835681 Protein, zinc finger FYVE-type containing 27 Protein, zinc finger FYVE domain containing 27 L homeolog Protein, zinc finger FYVE domain containing 27 Protein, zinc finger, FYVE domain containing 27 Protein, ZFYVE27 Protein, zfyve27.L Protein, zfyve27 Protein, Zfyve27 Protein
- Background
- This gene encodes a protein with several transmembrane domains, a Rab11-binding domain and a lipid-binding FYVE finger domain. The encoded protein appears to promote neurite formation. A mutation in this gene has been reported to be associated with hereditary spastic paraplegia, however the pathogenicity of the mutation, which may simply represent a polymorphism, is unclear.
- Molecular Weight
- 45.7 kDa
- NCBI Accession
- NP_653189
- Pathways
- Neurotrophin Signaling Pathway
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