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LHX4 antibody (AA 238-390)

This Rabbit Polyclonal antibody specifically detects LHX4 in WB, ELISA and FACS. It exhibits reactivity toward Human.
Catalog No. ABIN7872638
$625.62
Plus shipping costs $50.00
100 μg
Shipping to: United States
Delivery in 2 to 4 Business Days

Quick Overview for LHX4 antibody (AA 238-390) (ABIN7872638)

Target

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

Reactivity

  • 29
  • 6
  • 4
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
Human

Host

  • 23
  • 6
Rabbit

Clonality

  • 24
  • 5
Polyclonal

Conjugate

  • 24
  • 1
  • 1
  • 1
  • 1
  • 1
This LHX4 antibody is un-conjugated

Application

  • 26
  • 18
  • 5
  • 4
  • 4
  • 1
  • 1
  • 1
  • 1
  • 1
Western Blotting (WB), ELISA, Flow Cytometry (FACS)
  • Binding Specificity

    • 7
    • 3
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 238-390

    Purpose

    LHX4 Antibody / LIM homeobox protein 4

    Purification

    Antigen affinity purified

    Immunogen

    Recombinant human protein (amino acids S238-F390) was used as the immunogen for the LHX4 antibody.

    Isotype

    IgG
  • Application Notes

    Optimal dilution of the LHX4 antibody should be determined by the researcher.

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Buffer

    0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

    Storage

    4 °C,-20 °C

    Storage Comment

    After reconstitution, the LHX4 antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.
  • Target

    LHX4 (LIM Homeobox 4 (LHX4))

    Alternative Name

    LHX4

    Background

    LIM/homeobox protein Lhx4 is a protein that in humans is encoded by the LHX4 gene. 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 is a transcription factor involved in the control of differentiation and development of the pituitary gland. Mutations in this gene cause combined pituitary hormone deficiency 4.

    UniProt

    Q969G2
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