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Recombinant Human/Murine/Rat G

DF-11
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  • 询价
  • PeproTech
  • 120-11-5ug
  • 美国
  • 2025年12月11日
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    • 详细信息
    • 文献和实验
    • 技术资料
    • 供应商

      嵘崴达

    • 库存

      需确认

    • 英文名

      Recombinant Human/Murine/Rat GDF-11

    • 规格

      5ug

    产品概述

    GDF-11 is a myostatin-homologous protein that acts as an inhibitor of nerve tissue growth. GDF-11 has been shown to suppress neurogenesis through a myostatin-like pathway, which involves the arrest of the progenitor cell cycle in the G1 phase. Similarities between myostatin and GDF-11, which are 90% identical in their amino acid sequence, suggest that the regulatory mechanisms responsible for maintaining proper tissue size during neural and muscular development might be the same. Recombinant Human/Murine/Rat GDF-11 is a 25.0 kDa disulfide-linked homodimer containing two 109 amino acid polypeptide chains. It is highly homologous to myostatin/GDF-8, sharing 90% amino acid sequence identity.

    Source:E.coli

     

    Synonyms:Growth/Differentiation Factor-11, BMP-11

     

    AA Sequence (monomer):NLGLDCDEHS SESRCCRYPL TVDFEAFGWD WIIAPKRYKA NYCSGQCEYM FMQKYPHTHL VQQANPRGSA GPCCTPTKMS PINMLYFNDK QQIIYGKIPG MVVDRCGCS

     

    Purity:≥ 98% by SDS-PAGE gel and HPLC analyses.

     

    Biological Activity:Assay #1: Determined by its ability to inhibit induced alkaline phosphatase production by ATDC-5 chondrogenic cells. The expected ED50 for this effect is 0.08-0.10 µg/ml.

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    图标文献和实验
    相关实验
    • CD11a/CD11b/CD11c分子

      CD11a/CD11b/CD11c 分子 CDlla 常用单克隆抗体或代号:MHM24, 2F12; CRIS―3(LFA―lα链,整合素α1) 主要表达细胞:Leu[A5] 分子质量(kDa)和结构:spl80(整合素α) 功 能:与1CAM-l(CD54)、ICAM-2(CDl02)、ICAM-3(C1350)结合,介导细胞黏附;与JAMl结合,参与白细胞穿过内皮细胞

    • Expression and Preparation of Fusion Proteins from Recombinant gt11 Phages

      The phage λgt11 system has become increasingly popular for expression of cDNAs or genomic DNAs either in phage plaques or in bacteria lysogenized with recombinant phages (1 ,2 ). It offers the advantages of high cloning efficiency, high-level

    • Preparation and Ligand Screening of a gt11 Lysogen Library

      The λgt11 system has been designed to allow expression of cDNAs either in phage plaques or in bacteria lysogenized with recombinant λgtll phages (1 , 2 ). cDNAs are cloned into a unique EcoRl restriction site near the 3′ end of a truncated

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