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Recombinant Human GMCSF protei

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  • ¥1290 - 3960
  • 帛科
  • BK-DB7106
  • 国产
  • 2025年07月13日
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    • 详细信息
    • 文献和实验
    • 技术资料
    • 库存

      41

    • 英文名

      Recombinant Human GMCSF protein

    • 保质期

      12个月

    • 供应商

      上海帛科

    • 保存条件

      -20 to -80 °C

    • 规格

      50μg、100ug 、1mg

    商品介绍:
    货号 BK-DB7106 用途 仅供科研研究实验
    纯度 >90% as determined by SDS-PAGE 预测分子量 16.11 kDa
    表达宿主 E.coli 种属 Homo sapiens (Human)
    内毒素: Please contact with the lab for this information.
    蛋白构建: A DNA sequence encoding the human GMCSF (Ala18-Glu144) was fused with His tag
    制剂: Supplied as solution form  in  PBS pH 7.5 or lyophilized  from PBS pH 7.5.
    运输方式: In general, proteins are provided as lyophilized powder/frozen liquid. They are shipped out with dry ice/blue ice unless customers require otherwise.
    稳定性&储存: Use a manual defrost freezer and avoid repeated freeze thaw cycles.Store at 2 to 8 °C for one week .Store at -20 to -80 °C for twelve months from the date of receipt.
    复溶: Reconstitute in sterile water for a stock solution.A copy of datasheet will be provided with the products, please refer to it for details.
    分子别名: Granulocyte-macrophage colony-stimulating factor,GM-CSF,Colony-stimulating factor,CSF,Molgramostin,Sargramostim.
    背景介绍: Macrophage colony-stimulating factor 1, also known as CSF-1, M-CSF, Lanimostim and CSF1, is a single-pass membrane protein which is disulfide-linked as a homodimer or heterodimer. Granulocyte / macrophage colony-stimulating factors are cytokines that act in hematopoiesis by controlling the production, differentiation, and function of 2 related white cell populations of the blood, the granulocytes and the monocytes-macrophages. M-CSF/CSF-1 is known to facilitate monocyte survival, monocyte-to-macrophage conversion, and macrophage proliferation. M-CSF/CSF-1 is a secreted cytokine which influences hemopoietic stem cells to differentiate into macrophages or other related cell types. It binds to the Colony stimulating factor 1 receptor. M-CSF/CSF-1 may also be involved in development of the placenta. The active form of M-CSF/CSF-1 is found extracellularly as a disulfide-linked homodimer, and is thought to be produced by proteolytic cleavage of membrane-bound precursors. M-CSF/CSF-1 induces cells of the monocyte/macrophage lineage. It also plays a role in immunological defenses, bone metabolism, lipoproteins clearance, fertility and pregnancy. Upregulation of M-CSF/CSF-1 in the infarcted myocardium may have an active role in healing not only through its effects on cells of monocyte/macrophage lineage, but also by regulating endothelial cell chemokine expression.
    重组蛋白质的可溶性鉴定:
    1. 将按上法诱导培养后收集的菌体重悬于裂解液 1 (Lysis buffer under native conditions )中,然后在-80 oC 低温冰箱中放置 10 min。
    2. 冰中解冻。
    3. 在冰浴上用超声破碎仪破菌 6 次, 每次 10 sec,间歇 10 sec,电压 200-300 V。
    4. 10000g,4oC,离心 20min,取上清(为溶液 A), - 20 oC 保存; 另将沉淀用 同样裂解液 1 溶解(为溶液 B),同样 -20 oC 保存,供后继分析使用。
    5. 将上述 A、B 溶液和诱导前后的细菌进行 SDS-PAGE 电泳, 考马斯亮蓝染色, 比较分析重组蛋白质的溶解性。如果诱导表达的蛋白质位于 A 溶液中, 则为可溶性蛋白;如果是在 B 溶液中,则为非可溶蛋白。

    产品细节图片1
    重组蛋白质的分离纯化:
    1. 将菌体沉淀溶于适量裂解液 2(Lysis buffer under denaturing conditions )中,室温下搅拌和吹打沉淀,避免泡沫生成。
    2. 10000g ,4 oC,离心 30 min,收集上清液。
    3. 将 Ni-NTAAgarose 充填柱子,并连接于 Pharmarcia 低压液相层析系统,用 5 倍柱体积的裂解液 2 平衡 Ni-NTAAgarose,调节 A280 值至零线。
    4. 将适量上清液上样到 Ni-NTAAgarose 柱子中, 并用 lysis buffer 冲洗至 A280 值低于 0.01。
    5. 分别用 5 ~ 10 倍柱体积的清洗液 1 和清洗液 2(Washbuffer 1 and 2)清洗柱 子,直至 A280 值低于 0.01。
    6. 用洗脱液(Elution buffer)洗脱重组蛋白质, 在 A280 值监测下,收集出现峰 线后含有重组蛋白的所有洗脱液。

    产品细节图片2
    表达载体在基因工程有以下几种元件:
    (1)选择标志的编码序列;
    (2)可控转录的启动子;
    (3)转录调控序列(转录终止子,核糖体结合位点);
    (4)一个多限制酶切位点接头;
    (5)宿主体内自主复制的序列。

    产品细节图片3
    重组蛋白质的诱导表达:
    1. 挑取转化有质粒的单菌落, 接种于 3ml 选择性 LB 液体培养基中, 37 oC,250 rpm/min 振摇培养过夜。
    2. 次日将培养过夜的菌液 500 μl 再接种于 10ml(1:20)选择性 LB 液体培养基 中, 37 oC,250 rpm/min 振摇培养至光密度(OD600=0.6)时,取 1 ml 样本作 为诱导前标本, 10000g 离心 1min 收集菌体沉淀,-20 oC 冻存备用。
    3. 加入 1 mol/L IPTG 于菌液中,使 IPTG 终浓度为 1 mM ,37 oC ,250 rpm/min 振摇培养 4 ~ 5 小时。取 1 ml 样本作为诱导后标本,同上法收集菌体沉淀, -20 oC 冻存备用。
    4. 将诱导前后菌体沉淀用 20 ~ 40 μl PBS(pH= 8.0)重悬, 加入等体积的 2×SDS 上样缓冲液, 煮沸加热 5min,SDS 聚凝胶(SDS-PAGE)电泳分离 , 考马斯亮蓝染色 3 小时后,脱色观察结果。
    5. 选取诱导成功的细菌克隆,扩大诱导规模,收集菌体沉淀,于- 20 oC 保存,准备做下一步分析及纯化。
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