TRIM17/RNF16 Antibody Blocking Peptide(bs-9162P)-500ug

TRIM17/RNF16 Antibody Blocking

Peptide(bs-9162P)-500ug
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  • ¥880
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  • bs-9162P
  • 2025年10月16日
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      500ug

    产品编号bs-9162P
    英文名称TRIM17/RNF16 Antibody Blocking Peptide
    中文名称环指蛋白16封闭多肽
    英文别名RBCC; RING finger protein 16; RNF16; TERF; Testis RING finger protein; TRIM 17; Tripartite motif protein 17; TRI17_MOUSE.
    纯化方法HPLC
    研究领域

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

    Epigenetics and Nuclear Signaling > Transcription > Transcription Factors

    亚基Interacts (via coiled coil) with TRIM44 (via coiled coil).
    组织特异性Almost exclusively in the testis.
    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 B30.2/SPRY domain.
    Contains 1 RING-type zinc finger.
    功能May function as an ubiquitin E3 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The tripartite motif (TRIM) family of proteins are characterized by a conserved TRIM domain that includes a coiled-coil region, a B-box type zinc finger, one RING finger and three zinc-binding domains. TRIM17 (tripartite motif-containing 17), also known as RBCC, terf or RNF16, is a 477 amino acid protein that contains one RING-type zinc finger, one SPRY domain and one B box-type zinc finger. Expressed nearly exclusively in testis, TRIM17 belongs to the TRIM family and, based on its functional domains, may play a role in transcriptional regulation events. The gene encoding TRIM17 maps to human chromosome 1, which spans 260 million base pairs, contains over 3,000 genes and comprises nearly 8% of the human genome. Chromosome 1 houses a large number of disease-associated genes, including those that are involved in familial adenomatous polyposis, Stickler syndrome, Parkinson’s disease, Gaucher disease, schizophrenia and Usher syndrome. Aberrations in chromosome 1 are found in a variety of cancers, including head and neck cancer, malignant melanoma and multiple myeloma.

     

     

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