AIPL1 Antibody Blocking Peptide(bs-12452P)-500ug

AIPL1 Antibody Blocking Peptid

e(bs-12452P)-500ug
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  • bs-12452P
  • 2025年10月16日
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      500ug

    产品编号bs-12452P
    英文名称AIPL1 Antibody Blocking Peptide
    中文名称遗传性失明相关蛋白AIPL1封闭多肽
    英文别名A930007I01Rik; Aipl1; AIPL1_HUMAN; AIPL2; Aryl hydrocarbon interacting protein like 1; Aryl hydrocarbon receptor interacting protein like 1; Aryl-hydrocarbon-interacting protein-like 1; LCA4; MGC25485; OTTHUMP00000128207; OTTMUSP00000006382; RP23-401C17.1.
    纯化方法HPLC
    研究领域

    Neuroscience > Sensory System > Visual system

    Signal Transduction > Protein Trafficking > Chaperones > Other Chaperones

    亚基Interacts with NUB1.
    亚细胞定位Cytoplasm. Nucleus.
    组织特异性Highly expressed in retina. Specifically localized to the developing photoreceptor layer and within the photoreceptors of the adult retina.
    相似性Contains 1 PPIase FKBP-type domain.
    Contains 3 TPR repeats.
    功能May be important in protein trafficking and/or protein folding and stabilization.
    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 inherited blindness associated protein, aryl hydrocarbon receptor interacting protein-like 1 (AIPL1), interacts with the cell cycle regulator protein NUB1. AIPL1 is crucial for protein folding and stabilization, as well as for protein trafficking. It localizes to the nucleus or cytoplasm and is highly expressed in the pineal gland and the retina. In the retina, AIPL1 is expressed in both developing cone and rod photoreceptors, but it is restricted to rod photoreceptors in the adult human retina. Defects in the gene encoding for AIPL1 can cause Leber congenital amaurosis type IV, an early-onset, inherited autosomal recessive disorder that results in childhood blindness.

     

     

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