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供应Anti-E2F1(Thr433)抗体,磷酸化转录因子E2F1抗体
面议供应Anti-ATRIP (Ser68+Ser72)抗体,磷酸化系统性红斑狼疮先关蛋白TREX1抗体
面议供应Anti-SNAIL/SLUG(Ser246)抗体,磷酸化锌指转录因子Slug/SNAIL抗体
面议供应Anti-CSEN (Ser63) 抗体,磷酸化钾通道相互作用蛋白3抗体
面议供应Anti-ATRIP(Ser224)抗体,磷酸化系统性红斑狼疮相关蛋白TREX1抗体
面议检测Anti-Tau protein(Ser739)抗体,磷酸化微管相关蛋白抗体
面议检测Anti-TSFP1/SP1(Thr453)抗体,磷酸化转录生长因子SP1抗体
面议检测Anti-PTPN6(Tyr564)抗体,磷酸化蛋白*磷酸酶1C抗体
面议检测Anti-Tau protein(Thr529)抗体,磷酸化微管相关蛋白抗体
面议检测磷酸化APP(Tyr757)淀粉样肽前体蛋白抗体
面议检测Anti-GluR1(Ser863)抗体,磷酸化*受体1抗体
面议检测Anti-Androgen Receptor(Ser578)抗体,磷酸化雄激素受体抗体
面议本公司,是专业经营生物试剂,抗体,细胞,标准品,对照品的公司,在广大用户的帮助和支持下,经过不懈的努力,已成为国内生命科学领域产品的主要供应商之一,代理许多*水平的高科技产品,包括分子生物学、细胞生物学、免疫学、诊断等多个研究及应用领域。公司的服务和业务网络遍及全国,在同行获得*好评。
Anti-TRIM32/BBS11抗体,神经干细胞抑制相关蛋白TRIM32抗体简单介绍:
产品别名:72 kda Tat interacting Protein; BBS11; HT2A; LGMD2H; Limb girdle muscular dystrophy 2H (autosomal recessive); Limb girdle muscular dystrophy 2H; Muscular dystrophy Hutterite type; TAT interactive protein 72KD; TATIP; Tripartite Motif Containing Protein 32; Zinc Finger Protein HT2A; TRI32_MOUSE.
产品用途:科研实验
产品编号:BYK-0964R
性 状:Lyophilized or Liquid
浓 度:1mg/1ml
亚 型:IgG
贮 存:贮存于-20℃.
此抗体本公司有单抗和多抗,可用于免疫组化(IHC),免疫印迹(WB),酶联免疫(ELISA),IF、IP、流式细胞术等实验(可来电索取说明)
相关标记有:Alexa Fluor 350 标记、Alexa Fluor 488 标记、Alexa Fluor 555 标记、Alexa Fluor 647 标记、AP标记、APC标记、Biotin标记、Cy3标记、Cy5标记、Cy5.5标记、Cy7标记、FITC标记、Gold标记、HRP标记、PE标记、PE-Cy3标记、PE-CY5标记、PE-CY5.5标记、PE-CY7标记、RBITC标记
Anti-TRIM32/BBS11抗体,神经干细胞抑制相关蛋白TRIM32抗体产品说明:Tripartite motif-containing protein 32 (TRIM32) belongs to the tripartite motif (TRIM) protein family. TRIM32, like all TRIM proteins, contains a domain structure composed of a B-box, a RING-finger and a coiled-coil motif. Additionally, TRIM32 has six C-terminal NHL domains; it is expressed mainly in the skeletal muscle. The TRIM32 gene encodes an E3 ubiquitin ligase, a protein that attaches ubiquitin to a lysine residue on a target protein and acts in conjunction with ubiquitin-conjugating enzymes UbcH5a, UbcH5c and UbcH6. Mutations in the TRIM32 gene cause two forms of autosomal recessive muscular dystrophy designated limb girdle muscular dystrophy type 2H (LGMD2H) and sarcotubular myopathy (STM). TRIM32 mutations can also result in Bardet-Biedl syndrome (BBS), an autosomal recessive disorder characterized by pigmentary retinopathy, polydactyly, hypogenitalism, renal abnormalities, learning disabilities and obesity.
保存条件:Store at -20 °C for one year. Avoid repeated freeze/thaw cycles. The lyophilized antibody is stable at room temperature for at least one month and for greater than a year when kept at -20°C. When reconstituted in sterile pH 7.4 0.01M PBS or diluent of antibody the antibody is stable for at least two weeks at 2-4 °C.
连续使用时4°C存储,保质期六个月补体C1qα链多肽抗体*存储时建议分装为10ul以上小包装-20°C存储,并避免反复冻融,保质期一年。
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