ZFYVE27 Protein (Transcript Variant 5) (Myc-DYKDDDDK Tag)

Produktnummer ABIN2735876

Produktdetails

Target: ZFYVE27 (Zinc Finger, FYVE Domain Containing 27 (ZFYVE27))

Protein-Typ: Recombinant

Proteineigenschaft: Transcript Variant 5

Spezies: Human

Quelle: HEK-293 Cells

Aufreinigungstag / Konjugat: Dieses ZFYVE27 Protein ist gelabelt mit Myc-DYKDDDDK Tag.

Applikation: Antibody Production (AbP), Standard (STD)

Produktmerkmale:

• Recombinant human ZFYVE27 (transcript variant 5) protein expressed in HEK293 cells.
• Produced with end-sequenced ORF clone

Reinheit: > 80 % as determined by SDS-PAGE and Coomassie blue staining

Anwendungsinformationen

Applikationshinweise: Recombinant human proteins can be used for:
Native antigens for optimized antibody production
Positive controls in ELISA and other antibody assays

Kommentare:

The tag is located at the C-terminal.

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

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.

Antigendetails

Target: ZFYVE27 (Zinc Finger, FYVE Domain Containing 27 (ZFYVE27))

Andere Bezeichnung: Zfyve27 (ZFYVE27 Produkte)

Synonyme: 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

Hintergrund: 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.

Molekulargewicht: 35.7

NCBI Accession: NP_001167591

Pathways: Neurotrophin Signalübertragung