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BOLL antibody

This anti-BOLL antibody is a Rabbit Polyclonal antibody detecting BOLL in WB. Suitable for Human.
Catalog No. ABIN7468058

Quick Overview for BOLL antibody (ABIN7468058)

Target

See all BOLL Antibodies
BOLL (Bol, Boule-Like (BOLL))

Reactivity

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Human

Host

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Rabbit

Clonality

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Polyclonal

Conjugate

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This BOLL antibody is un-conjugated

Application

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Western Blotting (WB)
  • Cross-Reactivity

    Mouse

    Purification

    Purified by antigen-affinity chromatography.

    Immunogen

    Recombinant protein encompassing a sequence within the center region of human BOLL. The exact sequence is proprietary.

    Isotype

    IgG
  • Application Notes

    WB: 1:500-1:3000. Optimal dilutions/concentrations should be determined by the researcher. Not tested in other applications.

    Comment

    Positive Control: mouse testis

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1 mg/mL

    Buffer

    0.1M Tris-Glycine ( pH 7), 20 % Glycerol, 0.01 % Thimerosal

    Preservative

    Thimerosal (Merthiolate)

    Precaution of Use

    This product contains Thimerosal (Merthiolate): a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Storage

    4 °C,-20 °C

    Storage Comment

    Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4°C. For long-term storage, aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.
  • Target

    BOLL (Bol, Boule-Like (BOLL))

    Alternative Name

    boule homolog, RNA binding protein

    Background

    Synonyms: boule homolog, RNA binding protein , BOULE

    Background: This gene belongs to the DAZ gene family required for germ cell development. It encodes an RNA-binding protein which is more similar to Drosophila Boule than to human proteins encoded by genes DAZ (deleted in azoospermia) or DAZL (deleted in azoospermia-like). Loss of this gene function results in the absence of sperm in semen (azoospermia). Histological studies demonstrated that the primary defect is at the meiotic G2/M transition. Two alternatively spliced transcript variants encoding distinct isoforms have been found for this gene. [provided by RefSeq]

    Molecular Weight

    31 kDa

    Gene ID

    66037

    UniProt

    Q8N9W6
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