Overview

  • Product name

  • Description

    Rabbit polyclonal to HOXA2
  • Host species

    Rabbit
  • Tested applications

    Suitable for: ICC/IFmore details
  • Species reactivity

    Reacts with: Human
    Predicted to work with: Mouse, Rat, Cow, Baboon, Common marmoset
  • Immunogen

    Recombinant fragment corresponding to Human HOXA2 aa 208-275.
    Sequence:

    QNSEGKCKSLEDSEKVEEDEEEKTLFEQALSVSGALLEREGYTFQQNALS QQQAPNGHNGDSQSFPVS


    Database link: O43364

  • Positive control

    • ICC/IF: U-2 OS cells.

Properties

  • Form

    Liquid
  • Storage instructions

    Shipped at 4°C. Store at +4°C short term (1-2 weeks). Upon delivery aliquot. Store at -20°C long term. Avoid freeze / thaw cycle.
  • Storage buffer

    pH: 7.20
    Preservative: 0.02% Sodium azide
    Constituents: 40% Glycerol, PBS
  • Concentration information loading...
  • Purity

    Immunogen affinity purified
  • Clonality

    Polyclonal
  • Isotype

    IgG
  • Research areas

Applications

Our Abpromise guarantee covers the use of ab222304 in the following tested applications.

The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.

Application Abreviews Notes
ICC/IF Use a concentration of 1 - 4 µg/ml.

PFA-fixed/Triton X-100 permeabilized

Target

  • Function

    Sequence-specific transcription factor which is part of a developmental regulatory system that provides cells with specific positional identities on the anterior-posterior axis.
  • Involvement in disease

    Defects in HOXA2 are a cause of microtia hearing impairment and cleft palate (MHICP) [MIM:612290]. Microtia is a congenital deformity of the outer ear and occurs in approximately one in 8'000-10'000 births. It is characterized by a small, abnormally shaped outer ear. It can be unilateral or bilateral. Syndromic forms of microtia occur in conjunction with other abnormalities. The most common associated malformations is the cleft palate, a congenital fissure of the soft and/or hard palate due to faulty fusion. Defects in HOXA2 are a cause of autosomal-recessive bilateral microtia, mixed symmetrical severe to profound hearing impairment and partial cleft palate.
  • Sequence similarities

    Belongs to the Antp homeobox family. Proboscipedia subfamily.
    Contains 1 homeobox DNA-binding domain.
  • Cellular localization

    Nucleus.
  • Information by UniProt
  • Database links

  • Alternative names

    • AI324701 antibody
    • homeo box A2 antibody
    • homeobox A2 antibody
    • Homeobox protein Hox-1K antibody
    • Homeobox protein Hox-A2 antibody
    • Hox-1.11 antibody
    • HOX1.11 antibody
    • HOX1K antibody
    • Hoxa-2 antibody
    • Hoxa11 antibody
    • HOXA2 antibody
    • HXA2_HUMAN antibody
    • MGC151482 antibody
    • MGC151484 antibody
    • RATHOX111A antibody
    see all

Images

  • PFA-fixed, Triton X-100 permeabilized U-2 OS (human bone osteosarcoma epithelial cell line) cells stained for HOXA2 (green) using ab222304 at 4 µg/ml in ICC/IF.

References

ab222304 has not yet been referenced specifically in any publications.

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