Phone:
+1 877 302 8632
Fax:
+1 888 205 9894 (Toll-free)
E-Mail:
orders@antibodies-online.com

HOXD10 antibody

This Rabbit Polyclonal antibody specifically detects HOXD10 in IF. It exhibits reactivity toward Human, Mouse and Rat.
Catalog No. ABIN7263687

Quick Overview for HOXD10 antibody (ABIN7263687)

Target

See all HOXD10 Antibodies
HOXD10 (Homeobox D10 (HOXD10))

Reactivity

  • 37
  • 26
  • 5
  • 4
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
Human, Mouse, Rat

Host

  • 40
  • 2
  • 1
Rabbit

Clonality

  • 41
  • 2
Polyclonal

Conjugate

  • 24
  • 4
  • 3
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This HOXD10 antibody is un-conjugated

Application

  • 31
  • 21
  • 12
  • 5
  • 3
  • 2
  • 1
  • 1
  • 1
Immunofluorescence (IF)
  • Characteristics

    Polyclonal Antibody

    Purification

    Affinity purification

    Immunogen

    Recombinant fusion protein of human HOXD10 (NP_002139.2).

    Isotype

    IgG
  • Application Notes

    IF 1:50-1:200

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1 mg/mL

    Buffer

    PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3

    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

    Storage Comment

    Store at -20°C. Avoid freeze / thaw cycles.
  • Target

    HOXD10 (Homeobox D10 (HOXD10))

    Alternative Name

    HOXD10

    Background

    This gene is a member of the Abd-B homeobox family and encodes a protein with a homeobox DNA-binding domain. It is included in a cluster of homeobox D genes located on chromosome 2. The encoded nuclear protein functions as a sequence-specific transcription factor that is expressed in the developing limb buds and is involved in differentiation and limb development. Mutations in this gene have been associated with Wilm's tumor and congenital vertical talus (also known as 'rocker-bottom foot' deformity or congenital convex pes valgus) and/or a foot deformity resembling that seen in Charcot-Marie-Tooth disease.

    Gene ID

    3236

    UniProt

    P28358
You are here:
Chat with us!