TRIM37 Antibody Blocking Peptide(bs-16733P)-500ug

TRIM37 Antibody Blocking Pepti

de(bs-16733P)-500ug
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  • bs-16733P
  • 2025年10月16日
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      500ug

    产品编号bs-16733P
    英文名称TRIM37 Antibody Blocking Peptide
    中文名称TRIM37蛋白封闭多肽
    英文别名E3 ubiquitin protein ligase TRIM37; E3 ubiquitin-protein ligase TRIM37; KIAA0898; MUL; MUL protein; Mulibrey nanism gene; Mulibrey nanism protein; POB 1; POB1; RING B box coiled coil protein; TEF 3; TEF3; TRI37_HUMAN; TRIM 37; Trim37; Tripartite motif containing 37; Tripartite motif containing 37 protein; Tripartite motif containing protein 37; Tripartite motif-containing protein 37.
    纯化方法HPLC
    研究领域

    Epigenetics and Nuclear Signaling > Chromatin Modifying Enzymes > Ubiquitylation

    Epigenetics and Nuclear Signaling > Transcription > Domain Families > Zinc Finger

    亚细胞定位Cytoplasm > perinuclear region. Peroxisome. Found in vesicles of the peroxisome. Aggregates as aggresomes, a perinuclear region where certain misfolded or aggregated proteins are sequestered for proteasomal degradation.
    组织特异性Ubiquitous.
    翻译后修饰Auto-ubiquitinated.
    相似性Belongs to the TRIM/RBCC family.
    Contains 1 B box-type zinc finger.
    Contains 1 MATH domain.
    Contains 1 RING-type zinc finger.
    功能E3 ubiquitin-protein ligase.
    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TRIM37 is a protein that localizes to peroxisomes and contains a tripartite motif (TRIM) and a tumor necrosis factor-receptor associated factor (TRAF) domain. The protein and gene forms of TRIM37 are highly conserved between human and mouse. TRIM37 is expressed at a low level in the liver, ovary, heart, lung, skeletal muscle, and kidney, while it is highly expressed in the testis and brain, where it may act as an E3 ubiquitin ligase. Mutations in the TRIM37 gene result in Mulibrey nanism, an autosomal recessive prenatal-onset growth disorder that causes characteristic dysmorphic craniofacial features, heart disease, cardiopathy, failure of sexual maturation, and hepatomegaly.

     

     

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