製品の概要

  • 製品名Anti-VSX1 antibody
    VSX1 一次抗体 製品一覧
  • 製品の詳細
    Rabbit polyclonal to VSX1
  • アプリケーション適用あり: WBmore details
  • 種交差性
    交差種: Human
  • 免疫原

    Synthetic peptide conjugated to KLH, corresponding to a region within internal sequence amino acids 124-154 of Human VSX1 (NP_055403.2, NP_955457.1).

  • ポジティブ・コントロール
    • K562 cell line lysate

製品の特性

アプリケーション

Our Abpromise guarantee covers the use of ab123993 in the following tested applications.

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

アプリケーション Abreviews 特記事項
WB 1/100 - 1/500. Predicted molecular weight: 38 kDa.

ターゲット情報

  • 機能Binds to the 37-bp core of the locus control region (LCR) of the red/green visual pigment gene cluster. May regulate the activity of the LCR and the cone opsin genes at earlier stages of development.
  • 組織特異性In the adult eye, expressed in lens, iris, ciliary body, choroid, optical nerve head and, most strongly, in retina, but not expressed in sclera and cornea. According to PubMed 11978762, expressed in adult retina but not in lens and cornea. Within adult retina, found exclusively in the inner nuclear layer. Isoform 1, isoform 2, isoform 3 and isoform 4 expressed in adult retina, but not in brain, heart, kidney, liver, lung, pancreas, placenta and skeletal muscle. Not expressed in thymus and spleen. Expressed in embryonic craniofacial tissue. Expressed in fetal (week 14) retina. Strongly expressed in neonatal retina (day 0), weakly in neonatal lens (day 0), choroid (day 0) and cornea (day 0, 4; month 9).
  • 関連疾患Defects in VSX1 are a cause of posterior polymorphous corneal dystrophy type 1 (PPCD1) [MIM:122000]. PPCD1 is a slowly progressive hereditary disorder of the corneal endothelium that leads to a variable degree of visual impairment usually in adulthood.
    Defects in VSX1 are a cause of keratoconus type 1 (KTCN1) [MIM:148300]. Keratoconus type 1 is a frequent corneal dystrophy with an incidence that varies from 50 to 230 per 100'000. The cornea assumes a conical shape as a result of a progressive non-inflammatory thinning of the corneal stroma. Keratoconus is most often an isolated sporadic condition with cases of autosomal dominant and autosomal recessive transmission.
  • 配列類似性Belongs to the paired homeobox family.
    Contains 1 CVC domain.
    Contains 1 homeobox DNA-binding domain.
  • 細胞内局在Nucleus.
  • Information by UniProt
  • 参照データベース
  • 別名
    • CAASDS antibody
    • Homeodomain protein RINX antibody
    • KTCN antibody
    • KTCN1 antibody
    • Posterior polymorphous corneal dystrophy antibody
    • PPCD antibody
    • PPD antibody
    • Retinal inner nuclear layer homeobox protein antibody
    • RINX antibody
    • Transcription factor VSX1 antibody
    • Visual system homeobox 1 antibody
    • Visual system homeobox 1 homolog, CHX10 like antibody
    • Visual system homeobox 1 homolog, CHX10 like (zebrafish) antibody
    • VSX1 antibody
    • VSX1_HUMAN antibody
    see all

Anti-VSX1 antibody 画像

  • Anti-VSX1 antibody (ab123993) at 1/100 dilution + K562 cell line lysate at 35 µg

    Predicted band size : 38 kDa

Anti-VSX1 antibody (ab123993) 使用論文

ab123993 has not yet been referenced specifically in any publications.

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