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CLN5 antibody (C-Term)

CLN5 Reactivity: Human, Rat, Cow, Dog, Guinea Pig, Horse, Pig, Rabbit Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN5517800
  • Target See all CLN5 Antibodies
    CLN5 (Ceroid-Lipofuscinosis, Neuronal 5 (CLN5))
    Binding Specificity
    • 15
    • 7
    • 7
    • 6
    • 5
    • 3
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    C-Term
    Reactivity
    Human, Rat, Cow, Dog, Guinea Pig, Horse, Pig, Rabbit
    Host
    • 42
    • 1
    Rabbit
    Clonality
    • 43
    Polyclonal
    Conjugate
    • 15
    • 5
    • 4
    • 4
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This CLN5 antibody is un-conjugated
    Application
    Please inquire
    Sequence
    DNETGIYYET WNVKASPEKG AETWFDSYDC SKFVLRTFNK LAEFGAEFKN
    Predicted Reactivity
    Cow: 77%, Dog: 79%, Guinea Pig: 79%, Horse: 86%, Human: 100%, Pig: 86%, Rabbit: 86%, Rat: 79%
    Purification
    Affinity purified
    Immunogen
    The immunogen is a synthetic peptide directed towards the C terminal region of human CLN5
    Top Product
    Discover our top product CLN5 Primary Antibody
  • Restrictions
    For Research Use only
  • Format
    Liquid
    Buffer
    Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.
    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
    -20 °C
    Storage Comment
    For short term use, store at 2-8°C up to 1 week. For long term storage, store at -20°C in small aliquots to prevent freeze-thaw cycles.
  • Target
    CLN5 (Ceroid-Lipofuscinosis, Neuronal 5 (CLN5))
    Alternative Name
    CLN5 (CLN5 Products)
    Synonyms
    NCL antibody, A730075N08Rik antibody, CLN5, intracellular trafficking protein antibody, ceroid-lipofuscinosis, neuronal 5 antibody, CLN5 antibody, Cln5 antibody
    Background
    This gene is one of eight which have been associated with neuronal ceroid lipofuscinoses (NCL). Also referred to as Batten disease, NCL comprises a class of autosomal recessive, neurodegenerative disorders affecting children. The genes responsible likely encode proteins involved in the degradation of post-translationally modified proteins in lysosomes. The primary defect in NCL disorders is thought to be associated with lysosomal storage function.

    Alias Symbols: NCL

    Protein Interaction Partner: ARHGAP36, FBXO27, SPNS1, SFXN3, SLC25A22, SEC61A1, FBXO6, PHGDH, GANAB, OS9, CDIPT, SLC25A13, CDS2, SLC25A11, XPO1, SLC25A1, SEL1L, RPN1, RCN2, HMGCS1, DBH, CLN5, CLGN, CANX, CALU, CALR, ATP2A2, ATP1A3, ARF4, SLC25A6, SLC25A5, SLC25A4, Dlg4, UBC, KRT8,

    Protein Size: 358
    Gene ID
    1203
    NCBI Accession
    NM_006493, NP_006484
    UniProt
    O75503
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