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LHX4 antibody

The Rabbit Polyclonal anti-LHX4 antibody has been validated for IHC (p). It is suitable to detect LHX4 in samples from Human.
Catalog No. ABIN7467790

Quick Overview for LHX4 antibody (ABIN7467790)

Target

See all LHX4 Antibodies
LHX4 (LIM Homeobox 4 (LHX4))

Reactivity

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  • 5
  • 3
  • 2
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  • 2
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  • 2
  • 1
  • 1
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Human

Host

  • 20
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Rabbit

Clonality

  • 21
  • 5
Polyclonal

Conjugate

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  • 1
This LHX4 antibody is un-conjugated

Application

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Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
  • Cross-Reactivity

    Human

    Purification

    Purified by antigen-affinity chromatography.

    Immunogen

    Recombinant protein encompassing a sequence within the center region of human Lhx4. The exact sequence is proprietary.

    Isotype

    IgG
  • Application Notes

    IHC-P: 1:100-1:1000. Optimal dilutions/concentrations should be determined by the researcher. Not tested in other applications.

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    0.65 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

    LHX4 (LIM Homeobox 4 (LHX4))

    Alternative Name

    LIM homeobox 4

    Background

    LIM homeobox 4 , CPHD4,This gene encodes a member of a large protein family which contains the LIM domain, a unique cysteine-rich zinc-binding domain. The encoded protein may function as a transcriptional regulator and be involved in control of differentiation and development of the pituitary gland. Mutations in this gene are associated with syndromic short stature and pituitary and hindbrain defects. An alternative splice variant has been described but its biological nature has not been determined. [provided by RefSeq]

    Molecular Weight

    43 kDa

    Gene ID

    89884

    UniProt

    Q969G2
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