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ABHD11 antibody (Middle Region)

The Rabbit Polyclonal anti-ABHD11 antibody has been validated for WB and EIA. It is suitable to detect ABHD11 in samples from Human.
Catalog No. ABIN950210

Quick Overview for ABHD11 antibody (Middle Region) (ABIN950210)

Target

See all ABHD11 Antibodies
ABHD11 (Abhydrolase Domain Containing 11 (ABHD11))

Reactivity

  • 23
  • 7
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Human

Host

  • 26
  • 2
Rabbit

Clonality

  • 28
Polyclonal

Conjugate

  • 12
  • 3
  • 3
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This ABHD11 antibody is un-conjugated

Application

  • 16
  • 15
  • 8
  • 2
  • 1
Western Blotting (WB), Enzyme Immunoassay (EIA)
  • Binding Specificity

    • 7
    • 5
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 183-213, Middle Region

    Specificity

    This antibody reacts to ABHD11.

    Cross-Reactivity (Details)

    Species reactivity (tested):Human.

    Purification

    Affinity chromatography on Protein A

    Immunogen

    KLH conjugated synthetic peptide between 183~213 amino acids from the Central region of human ABHDB

    Isotype

    Ig Fraction
  • Application Notes

    Optimal working dilution should be determined by the investigator.

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    0.25 mg/mL

    Buffer

    PBS containing 0.09 % (W/V) sodium azide as preservative

    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 freezing and thawing.

    Storage

    4 °C/-20 °C

    Storage Comment

    Store the antibody undiluted at 2-8 °C for one month or (in aliquots) at -20 °C for longer.
  • Target

    ABHD11 (Abhydrolase Domain Containing 11 (ABHD11))

    Alternative Name

    ABHD11

    Background

    ABHDB encodes a protein containing an alpha/beta hydrolase fold domain. This protein is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23.Synonyms: Abhydrolase domain-containing protein 11, PP1226, WBSCR21

    Gene ID

    83451

    NCBI Accession

    NP_001138836
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