ZFYVE26 Antikörper (C-Term)

Produktnummer ABIN783824

Produktdetails anti-ZFYVE26 Antikörper

Target: ZFYVE26 (Zinc Finger, FYVE Domain Containing 26 (ZFYVE26))

Bindungsspezifität: C-Term

Reaktivität: Human, Maus, Ratte

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser ZFYVE26 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB), Enzyme Immunoassay (EIA)

Spezifität: This antibody reacts to ZFYVE26.

Aufreinigung: Affinity chromatography

Immunogen: 16 amino acid peptide near the carboxy terminus of human SPG15.

Anwendungsinformationen

Applikationshinweise: Optimal working dilution should be determined by the investigator.

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Konzentration: 1,0 mg/mL

Buffer: PBS containing 0.02 % sodium azide as preservative

Konservierungsmittel: Sodium azide

Vorsichtsmaßnahmen: This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Lagerung: 4 °C

Informationen zur Lagerung: Store the antibody undiluted at 2-8 °C.

Details zu ZFYVE26

Target: ZFYVE26 (Zinc Finger, FYVE Domain Containing 26 (ZFYVE26))

Andere Bezeichnung: ZFYVE26 (ZFYVE26 Produkte)

Synonyme: wu:fc33a03 antikoerper, FYVE-CENT antikoerper, SPG15 antikoerper, 4930465A13 antikoerper, 9330197E15Rik antikoerper, A630028O16Rik antikoerper, Gm893 antikoerper, mKIAA0321 antikoerper, zinc finger, FYVE domain containing 26 antikoerper, zinc finger FYVE-type containing 26 antikoerper, zfyve26 antikoerper, ZFYVE26 antikoerper, Zfyve26 antikoerper

Hintergrund: Hereditary spastic paraplegias (HSPs) are genetically and phenotypically heterogeneous disorders. Spastic paraplegia with thinning of the corpus callosum (ARHSP-TCC) is a relatively frequent form of complicated hereditary spastic paraplegia in which mental retardation and muscle stiffness at onset are followed by slowly progressive paraparesis and cognitive deterioration. SPG15 is the second gene known to be responsible for ARHSP-TCC in the Italian population. Mutations in this gene are associated with autosomal recessive spastic paraplegia-15. SPG15 encodes a protein containing a FYVE zinc finger binding domain which is thought to target these proteins to membrane lipids through interaction with phospholipids in the membrane. SPG15 mRNA is widely distributed in human tissues, as well as in rat embryos, suggesting a possible role for this protein during embryonic development. SPG15 co-localizes partially with endoplasmic reticulum and endosome markers, suggesting a role in intracellular trafficking. Multiple isoforms of SPG15 are known to exist.Synonyms: KIAA0321, Zinc finger FYVE domain-containing protein 26

Gen-ID: 23503

NCBI Accession: NP_056161

UniProt: Q68DK2