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AGA antibody (Middle Region)

AGA Reactivity: Human, Rat, Cow, Dog, Guinea Pig, Horse, Pig WB Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN2788660
  • Target See all AGA Antibodies
    AGA (Aspartylglucosaminidase (AGA))
    Binding Specificity
    • 6
    • 1
    • 1
    • 1
    • 1
    Middle Region
    Reactivity
    • 19
    • 11
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Human, Rat, Cow, Dog, Guinea Pig, Horse, Pig
    Host
    • 19
    • 1
    Rabbit
    Clonality
    • 20
    Polyclonal
    Conjugate
    • 9
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This AGA antibody is un-conjugated
    Application
    • 10
    • 7
    • 4
    • 2
    • 2
    • 1
    Western Blotting (WB)
    Sequence
    SMGFINEDLS TTASQALHSD WLARNCQPNY WRNVIPDPSK YCGPYKPPGI
    Predicted Reactivity
    Cow: 86%, Dog: 79%, Guinea Pig: 85%, Horse: 79%, Human: 100%, Pig: 86%, Rat: 79%
    Characteristics
    This is a rabbit polyclonal antibody against AGA. It was validated on Western Blot.
    Purification
    Affinity Purified
    Top Product
    Discover our top product AGA Primary Antibody
  • Application Notes
    Optimal working dilutions should be determined experimentally by the investigator.
    Comment

    Antigen size: 336 AA

    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    Lot specific
    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.
    Handling Advice
    Avoid repeated freeze-thaw cycles.
    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
    AGA (Aspartylglucosaminidase (AGA))
    Alternative Name
    AGA (AGA Products)
    Background
    Aspartylglucosaminidase is involved in the catabolism of N-linked oligosaccharides of glycoproteins. It cleaves asparagine from N-acetylglucosamines as one of the final steps in the lysosomal breakdown of glycoproteins. The lysosomal storage disease aspartylglycosaminuria is caused by a deficiency in the AGA enzyme.
    Alias Symbols: AGU, ASRG, GA
    Protein Interaction Partner: FBXO6, ALB, AGA, IGF2R,
    Protein Size: 336
    Molecular Weight
    36 kDa
    Gene ID
    175
    NCBI Accession
    NM_001171988, NP_001165459
    UniProt
    P20933
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