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ALX4 antibody

The Rabbit Polyclonal anti-ALX4 antibody has been validated for ELISA and IHC. It is suitable to detect ALX4 in samples from Human.
Catalog No. ABIN7189784

Quick Overview for ALX4 antibody (ABIN7189784)

Target

See all ALX4 Antibodies
ALX4 (ALX Homeobox 4 (ALX4))

Reactivity

  • 34
  • 11
  • 8
  • 6
  • 5
  • 4
  • 4
  • 4
  • 2
  • 2
  • 1
  • 1
  • 1
Human

Host

  • 31
  • 4
Rabbit

Clonality

  • 31
  • 4
Polyclonal

Conjugate

  • 21
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This ALX4 antibody is un-conjugated

Application

  • 24
  • 12
  • 9
  • 3
  • 1
  • 1
  • 1
  • 1
ELISA, Immunohistochemistry (IHC)
  • Purpose

    ALX4 Antibody

    Cross-Reactivity

    Mouse

    Purification

    Antigen affinity purification

    Immunogen

    Synthetic peptide of Human ALX4

    Isotype

    IgG
  • Application Notes

    Optimal working dilution should be determined by the investigator.

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

     pH 7.4 PBS, 0.05 % Sodium azide, 40 % Glycerol

    Preservative

    Sodium azide

    Precaution of Use

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

    Storage

    -20 °C,-80 °C

    Storage Comment

    Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
  • Target

    ALX4 (ALX Homeobox 4 (ALX4))

    Alternative Name

    ALX4

    Background

    Background: This gene encodes a paired-like homeodomain transcription factor expressed in the mesenchyme of developing bones, limbs, hair, teeth, and mammary tissue. Mutations in this gene cause parietal foramina 2 (PFM2), an autosomal dominant disease characterized by deficient ossification of the parietal bones. Mutations in this gene also cause a form of frontonasal dysplasia with alopecia and hypogonadism, suggesting a role for this gene in craniofacial development, mesenchymal-epithelial communication, and hair follicle development. Deletion of a segment of chromosome 11 containing this gene, del(11)(p11p12), causes Potocki-Shaffer syndrome (PSS), a syndrome characterized by craniofacial anomalies, mental retardation, multiple exostoses, and genital abnormalities in males. In mouse, this gene has been shown to use dual translation initiation sites located 16 codons apart.

    Aliases: Alx4 antibody, ALX4_HUMAN antibody, Aristaless like homeobox 4 antibody, CRS5 antibody, FND2 antibody, FPP antibody, homeobox protein aristaless like 4 antibody, Homeobox protein aristaless-like 4 antibody, homeodomain transcription factor ALX4 antibody, KIAA1788 antibody, PFM1 antibody, PFM2 antibody

    UniProt

    Q9H161
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