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RNASEH2C antibody (AA 1-164)

RNASEH2C Reactivity: Human WB Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN6146992
  • Target See all RNASEH2C Antibodies
    RNASEH2C (Ribonuclease H2, Subunit C (RNASEH2C))
    Binding Specificity
    • 7
    • 7
    • 7
    • 6
    • 6
    • 1
    • 1
    AA 1-164
    Reactivity
    Human
    Host
    • 23
    • 1
    Rabbit
    Clonality
    • 23
    • 1
    Polyclonal
    Conjugate
    • 10
    • 4
    • 3
    • 3
    • 2
    • 2
    This RNASEH2C antibody is un-conjugated
    Application
    • 20
    • 19
    • 13
    • 4
    • 3
    • 1
    • 1
    • 1
    Western Blotting (WB)
    Sequence
    MESGDEAAIE RHRVHLRSAT LRDAVPATLH LLPCEVAVDG PAPVGRFFTP AIRQGPEGLE VSFRGRCLRG EEVAVPPGLV GYVMVTEEKK VSMGKPDPLR DSGTDDQEEE PLERDFDRFI GATANFSRFT LWGLETIPGP DAKVRGALTW PSLAAAIHAQ VPED
    Cross-Reactivity
    Human
    Characteristics
    Polyclonal Antibodies
    Immunogen
    Recombinant fusion protein containing a sequence corresponding to amino acids 1-164 of human RNASEH2C (NP_115569.2).
    Isotype
    IgG
    Top Product
    Discover our top product RNASEH2C Primary Antibody
  • Application Notes
    WB,1:500 - 1:2000
    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
    RNASEH2C (Ribonuclease H2, Subunit C (RNASEH2C))
    Alternative Name
    RNASEH2C (RNASEH2C Products)
    Synonyms
    AGS3 antibody, AYP1 antibody, 1500026D16Rik antibody, ribonuclease H2 subunit C antibody, ribonuclease H2, subunit C antibody, RNASEH2C antibody, Rnaseh2c antibody
    Background
    This gene encodes a ribonuclease H subunit that can cleave ribonucleotides from RNA:DNA duplexes. Mutations in this gene cause Aicardi-Goutieres syndrome-3, a disease that causes severe neurologic dysfunction. A pseudogene for this gene has been identified on chromosome Y, near the sex determining region Y (SRY) gene.,RNASEH2C,AGS3,AYP1,Epigenetics & Nuclear Signaling,RNASEH2C
    Molecular Weight
    17 kDa
    Gene ID
    84153
    UniProt
    Q8TDP1
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