Phone:
+1 877 302 8632
Fax:
+1 888 205 9894 (Toll-free)
E-Mail:
orders@antibodies-online.com

RD3 antibody (AA 1-195)

RD3 Reactivity: Human WB Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN6146834
  • Target See all RD3 Antibodies
    RD3 (Retinal Degeneration 3 (RD3))
    Binding Specificity
    • 6
    • 1
    • 1
    AA 1-195
    Reactivity
    • 8
    • 2
    • 1
    • 1
    Human
    Host
    • 9
    Rabbit
    Clonality
    • 9
    Polyclonal
    Conjugate
    • 5
    • 2
    • 1
    • 1
    This RD3 antibody is un-conjugated
    Application
    • 5
    • 5
    • 2
    Western Blotting (WB)
    Sequence
    MSLISWLRWN EAPSRLSTRS PAEMVLETLM MELTGQMREA ERQQRERSNA VRKVCTGVDY SWLASTPRST YDLSPIERLQ LEDVCVKIHP SYCGPAILRF RQLLAEQEPE VQEVSQLFRS VLQEVLERMK QEEEAHKLTR QWSLRPRGSL ATFKTRARIS PFASDIRTIS EDVERDTPPP LRSWSMPEFR APKAD
    Cross-Reactivity
    Mouse, Rat
    Characteristics
    Polyclonal Antibodies
    Immunogen
    Recombinant fusion protein containing a sequence corresponding to amino acids 1-195 of human RD3 (NP_898882.1).
    Isotype
    IgG
    Top Product
    Discover our top product RD3 Primary Antibody
  • Application Notes
    WB,1:500 - 1:1000
    Restrictions
    For Research Use only
  • Format
    Liquid
    Buffer
    PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.
    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
    Store at -20°C. Avoid freeze / thaw cycles.
  • Target
    RD3 (Retinal Degeneration 3 (RD3))
    Alternative Name
    RD3 (RD3 Products)
    Synonyms
    C1orf36 antibody, LCA12 antibody, 3322402L07Rik antibody, rd-3 antibody, rd3 antibody, retinal degeneration 3 antibody, RD3 antibody, Rd3 antibody
    Background
    This gene encodes a retinal protein that is associated with promyelocytic leukemia-gene product (PML) bodies in the nucleus. Mutations in this gene cause Leber congenital amaurosis type 12, a disease that results in retinal degeneration. Alternative splicing results in multiple transcript variants.,RD3,C1orf36,LCA12,Neuroscience,RD3
    Molecular Weight
    22 kDa
    Gene ID
    343035
    UniProt
    Q7Z3Z2
You are here:
Support