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ZFYVE26 antibody (C-Term)

ZFYVE26 Reactivity: Human, Mouse, Rat WB, EIA Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN783824
  • Target See all ZFYVE26 Antibodies
    ZFYVE26 (Zinc Finger, FYVE Domain Containing 26 (ZFYVE26))
    Binding Specificity
    • 5
    • 2
    • 1
    • 1
    • 1
    • 1
    C-Term
    Reactivity
    • 10
    • 3
    • 3
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Human, Mouse, Rat
    Host
    • 10
    Rabbit
    Clonality
    • 10
    Polyclonal
    Conjugate
    • 6
    • 2
    • 1
    • 1
    This ZFYVE26 antibody is un-conjugated
    Application
    • 6
    • 4
    • 2
    • 2
    • 2
    Western Blotting (WB), Enzyme Immunoassay (EIA)
    Specificity
    This antibody reacts to ZFYVE26.
    Purification
    Affinity chromatography
    Immunogen
    16 amino acid peptide near the carboxy terminus of human SPG15.
    Top Product
    Discover our top product ZFYVE26 Primary Antibody
  • Application Notes
    Optimal working dilution should be determined by the investigator.
    Restrictions
    For Research Use only
  • Concentration
    1,0 mg/mL
    Buffer
    PBS containing 0.02 % sodium azide as preservative
    Preservative
    Sodium azide
    Precaution of Use
    This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Storage
    4 °C
    Storage Comment
    Store the antibody undiluted at 2-8 °C.
  • Target
    ZFYVE26 (Zinc Finger, FYVE Domain Containing 26 (ZFYVE26))
    Alternative Name
    ZFYVE26 (ZFYVE26 Products)
    Synonyms
    wu:fc33a03 antibody, FYVE-CENT antibody, SPG15 antibody, 4930465A13 antibody, 9330197E15Rik antibody, A630028O16Rik antibody, Gm893 antibody, mKIAA0321 antibody, zinc finger, FYVE domain containing 26 antibody, zinc finger FYVE-type containing 26 antibody, zfyve26 antibody, ZFYVE26 antibody, Zfyve26 antibody
    Background
    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
    Gene ID
    23503
    NCBI Accession
    NP_056161
    UniProt
    Q68DK2
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