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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
$483.54
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Quick Overview for AGA antibody (Middle Region) (ABIN2788660)

Target

See all AGA Antibodies
AGA (Aspartylglucosaminidase (AGA))

Reactivity

  • 22
  • 13
  • 3
  • 1
  • 1
  • 1
  • 1
  • 1
Human, Rat, Cow, Dog, Guinea Pig, Horse, Pig

Host

  • 22
  • 1
Rabbit

Clonality

  • 23
Polyclonal

Conjugate

  • 12
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This AGA antibody is un-conjugated

Application

  • 12
  • 8
  • 5
  • 2
  • 2
  • 2
Western Blotting (WB)
  • Binding Specificity

    • 6
    • 2
    • 1
    • 1
    • 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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