• Product nameAnti-SOX3 antibody
    See all SOX3 primary antibodies
  • Description
    Mouse monoclonal to SOX3
  • Tested applicationsSuitable for: WBmore details
  • Species reactivity
    Reacts with: Human
    Predicted to work with: Mouse
  • Immunogen

    Recombinant fragment: KSEPSSPPPA IASHSQRACL GDLRDMISMY LPPGGDAADA ASPLPGGRLH GVHQHYQGAG TAVNGTVPLT H, corresponding to amino acids 375-446 of Human SOX3



Our Abpromise guarantee covers the use of ab55795 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
  • Application notesWB: Use at a concentration of 1-5 µg/ml.

    Not yet tested in other applications.
    Optimal dilutions/concentrations should be determined by the end user.
  • Target

    • FunctionTranscription factor required during the formation of the hypothalamo-pituitary axis. May function as a switch in neuronal development. Keeps neural cells undifferentiated by counteracting the activity of proneural proteins and suppresses neuronal differentiation. Required also within the pharyngeal epithelia for craniofacial morphogenesis. Controls a genetic switch in male development. Is necessary for initiating male sex determination by directing the development of supporting cell precursors (pre-Sertoli cells) as Sertoli rather than granulosa cells.
    • Involvement in diseaseDefects in SOX3 are a cause of panhypopituitarism X-linked (PHPX) [MIM:312000]. Affected individuals have absent infundibulum, anterior pituitary hypoplasia, and ectopic posterior pituitary.
      Defects in SOX3 are the cause of mental retardation X-linked with isolated growth hormone deficiency (MRXGH) [MIM:300123].
      Defects in SOX3 are the cause of 46,XX sex reversal type 3 (SRXX3) [MIM:300833]. A condition in which male gonads develop in a genetic female (female to male sex reversal). Note=Copy number variations (CNV) encompassing or in close proximity to SOX3 are responsible for XX male reversal. These variations include two duplications of approximately 123 kb and 85 kb, the former of which spans the entire SOX3 gene; a 343 kb deletion immediately upstream of SOX3 that is probably responsible of altered regulation (and not increased dosage) of SOX3; a large (approximately 6 Mb) duplication that encompasses SOX3 and at least 18 additional distally located genes. Its proximal breakpoint falls within the SOX3 regulatory region. This large rearrangement has been found in a patient with XX male reversal and a complex phenotype that also includes a scrotal hypoplasia, microcephaly, developmental delay, and growth retardation.
    • Sequence similaritiesContains 1 HMG box DNA-binding domain.
    • Cellular localizationNucleus.
    • Information by UniProt
    • Database links
    • Alternative names
      • GHDX antibody
      • MRGH antibody
      • PHP antibody
      • PHPX antibody
      • sox3 antibody
      • SOX3_HUMAN antibody
      • SOXB antibody
      • SRY (sex determining region Y)-box 3 antibody
      • SRY Box 3 antibody
      • SRY-related HMG-box gene 3 antibody
      • Transcription factor Sox-3 antibody
      see all

    Anti-SOX3 antibody images

    • Predicted band size : 45 kDa
      SOX3 antibody (ab55795) at 1ug/lane + A-431 cell lysate at 25ug/lane.

    References for Anti-SOX3 antibody (ab55795)

    ab55795 has not yet been referenced specifically in any publications.

    Product Wall

    Application IHC - Wholemount
    Sample Mouse Embryo (E9.5)
    Specification E9.5

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    Submitted Apr 11 2017