HESX1 Antibody Blocking Peptide(bs-13597P)-500ug

HESX1 Antibody Blocking Peptid

e(bs-13597P)-500ug
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  • bs-13597P
  • 2025年10月16日
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      500ug

    产品编号bs-13597P
    英文名称HESX1 Antibody Blocking Peptide
    中文名称同源结构域转录因子HESX1封闭多肽
    英文别名HESX1_HUMAN; Homeobox expressed in ES cells 1; Homeobox protein ANF; hAnf.
    纯化方法HPLC
    研究领域

    Developmental Biology > Embryogenesis > Embryonic stem cells > Surface molecules

    Epigenetics and Nuclear Signaling > Transcription > Domain Families > Developmental Families

    Epigenetics and Nuclear Signaling > Transcription > Transcription Factors

    Stem Cells > Embryonic Stem Cells > Intracellular

    亚基Can form heterodimers with PROP1 in binding to DNA (By similarity). Interacts with TLE1.
    亚细胞定位Nuclear
    相似性Belongs to the ANF homeobox family.
    Contains 1 homeobox DNA-binding domain.
    功能Required for the normal development of the forebrain, eyes and other anterior structures such as the olfactory placodes and pituitary gland. Possible transcriptional repressor. Binds to the palindromic PIII sequence, 5'-AGCTTGAGTCTAATTGAATTAACTGTAC-3'. HESX1 and PROP1 bind as heterodimers on this palindromic site, and, in vitro, HESX1 can antagonize PROP1 activation (By similarity).
    保存条件Shipped at 4℃. Stored at -20℃ for one year. Avoid repeated freeze/thaw cycles.
    注意事项This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
    背景资料The homeobox protein, HESX1, which is also known as Rathke’s pouch homeobox, HANF, homeodomain transcription factor, and anterior-restricted homeobox protein is a transcription factor that belongs to the homeodomain family of DNA binding proteins. HESX1 is initially expressed in embryonic stem cells and the primitive forebrain, and is essential for normal development of the eyes and other anterior CNS structures, such as the hypothalamus, the pituitary gland and the olfactory bulbs. The homeobox gene Hesx1 is expressed in the anterior visceral endoderm (AVE), anterior axial mesendoderm (AME), and anterior neural ectoderm (ANE) during early embryogenesis. Mutations in the Hesx1 gene are associated with disorders that are comparable with septo-optic dysplasia (SOD). These disorders are characterized by hypoplasia of the optic nerve, various types of forebrain defects and pituitary hormone deficiencies, including hypothyroidism. Hesx1 also acts as a transcriptional repressor of reporter gene constructs in tissue culture assays.

     

     

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