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AGA antibody (Middle Region)

This Rabbit Polyclonal antibody specifically detects AGA in WB. It exhibits reactivity toward Human, Rat, Cow, Dog, Guinea Pig, Horse and Pig.
Catalog No. ABIN2788660

Quick Overview for AGA antibody (Middle Region) (ABIN2788660)

Target

See all AGA Antibodies
AGA (Aspartylglucosaminidase (AGA))

Reactivity

  • 22
  • 12
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Human, Rat, Cow, Dog, Guinea Pig, Horse, Pig

Host

  • 23
  • 1
Rabbit

Clonality

  • 24
Polyclonal

Conjugate

  • 13
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This AGA antibody is un-conjugated

Application

  • 14
  • 9
  • 7
  • 4
  • 4
  • 1
Western Blotting (WB)
  • Binding Specificity

    • 7
    • 3
    • 2
    • 1
    • 1
    Middle Region

    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
  • 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

    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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