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AMPD1 antibody (AA 50-260)

This anti-AMPD1 antibody is a Rabbit Polyclonal antibody detecting AMPD1 in WB and IF. Suitable for Human.
Catalog No. ABIN1678653

Quick Overview for AMPD1 antibody (AA 50-260) (ABIN1678653)

Target

See all AMPD1 Antibodies
AMPD1 (Adenosine Monophosphate Deaminase 1 (AMPD1))

Reactivity

  • 30
  • 23
  • 22
  • 4
  • 2
  • 2
  • 2
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  • 2
Human

Host

  • 36
  • 1
Rabbit

Clonality

  • 37
Polyclonal

Conjugate

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  • 1
  • 1
  • 1
  • 1
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  • 1
  • 1
  • 1
  • 1
  • 1
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  • 1
  • 1
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This AMPD1 antibody is un-conjugated

Application

  • 13
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  • 3
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  • 1
Western Blotting (WB), Immunofluorescence (IF)
  • Binding Specificity

    • 15
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    • 1
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    AA 50-260

    Sequence

    AEKVFASEVK DEGGRQEISP FDVDEICPIS HHEMQAHIFH LETLSTSTEA RRKKRFQGRK TVNLSIPLSE TSSTKLSHID EYISSSPTYQ TVPDFQRVQI TGDYASGVTV EDFEIVCKGL YRALCIREKY MQKSFQRFPK TPSKYLRNID GEAWVANESF YPVFTPPVKK GEDPFRTDNL PENLGYHLKM KDGVVYVYPN EAAVSKDEPK P

    Cross-Reactivity

    Human, Mouse, Rat

    Characteristics

    Polyclonal Antibodies

    Purification

    Affinity purification

    Immunogen

    Recombinant fusion protein containing a sequence corresponding to amino acids 50-260 of human AMPD1 (NP_001166097.1).

    Isotype

    IgG
  • Application Notes

    WB,1:500 - 1:2000,IF,1:50 - 1:200

    Restrictions

    For Research Use only
  • 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

    AMPD1 (Adenosine Monophosphate Deaminase 1 (AMPD1))

    Alternative Name

    AMPD1

    Background

    Adenosine monophosphate deaminase 1 catalyzes the deamination of AMP to IMP in skeletal muscle and plays an important role in the purine nucleotide cycle. Two other genes have been identified, AMPD2 and AMPD3, for the liver- and erythocyte-specific isoforms, respectively. Deficiency of the muscle-specific enzyme is apparently a common cause of exercise-induced myopathy and probably the most common cause of metabolic myopathy in the human. Alternatively spliced transcript variants encoding different isoforms have been identified in this gene.,AMPD1,MAD,MADA,MMDD,Cancer,Signal Transduction,Endocrine & Metabolism,AMPD1

    Molecular Weight

    89 kDa/90 kDa

    Gene ID

    270

    UniProt

    P23109
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