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ACTL10 antibody (AA 21-100) (HRP)

This Rabbit Polyclonal antibody specifically detects ACTL10 in ELISA, IHC (fro) and IHC (p). It exhibits reactivity toward Rat.
Catalog No. ABIN1711234

Quick Overview for ACTL10 antibody (AA 21-100) (HRP) (ABIN1711234)

Target

ACTL10 (Actin-Like 10 (ACTL10))

Reactivity

Rat

Host

  • 14
Rabbit

Clonality

  • 14
Polyclonal

Conjugate

  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This ACTL10 antibody is conjugated to HRP

Application

  • 13
  • 13
  • 2
  • 2
  • 2
  • 1
ELISA, Immunohistochemistry (Frozen Sections) (IHC (fro)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
  • Binding Specificity

    AA 21-100

    Cross-Reactivity

    Rat

    Predicted Reactivity

    Human,Mouse

    Purification

    Purified by Protein A.

    Immunogen

    KLH conjugated synthetic peptide derived from human C20orf134

    Isotype

    IgG
  • Application Notes

    IHC-P 1:200-400
    IHC-F 1:100-500

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1 μg/μL

    Buffer

    Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.

    Preservative

    ProClin

    Precaution of Use

    This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.

    Handling Advice

    Do NOT add Sodium Azide! Use of Sodium Azide will inhibit enzyme activity of horseradish peroxidase.

    Storage

    -20 °C

    Storage Comment

    Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

    Expiry Date

    12 months
  • Target

    ACTL10 (Actin-Like 10 (ACTL10))

    Alternative Name

    C20orf134

    Background

    Synonyms: C20orf134, CT134_HUMAN, Putative uncharacterized actin family protein C20orf134.

    Background: C20orf134 is a 245 amino acid secreted protein that belongs to the Actin family and is encoded by a gene which maps to human chromosome 20. Comprising approximately 2 % of the human genome, chromosome 20 contains nearly 63 million bases that encode over 600 genes, some of which are associated with Creutzfeldt-Jakob disease, amyotrophic lateral sclerosis, spinal muscular atrophy, ring chromosome 20 epilepsy syndrome and Alagille syndrome. Additionally, chromosome 20 contains a region with numerous genes which are thought important for seminal production and may be potential targets for male contraception.

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