BD Transduction Laboratories™ Purified Mouse Anti-GM130 (610823)
用户验证的应用
经验证应用
| 项目 | 详情 |
|---|---|
| Application | Western blot (Routinely Tested), Immunofluorescence (Tested During Development), Immunohistochemistry, Immunoprecipitation (Not Recommended) |
推荐实验流程
Western blot: Please refer to http://www.bdbiosciences.com/pharmingen/protocols/Western_Blotting.shtml.
详细信息
制备与储存
The monoclonal antibody was purified from tissue culture supernatant or ascites by affinity chromatography. Store undiluted at -20°C.
荧光格式说明
Tissue culture supernatant is purified by either protein A/G or affinity purification methods. Both methods yield antibody in solution that is free of most other soluble proteins, lipids, etc. This format provides pure antibody that is suitable for a number of downstream applications including: secondary labeling for flow cytometry or microscopy, ELISA, Western blot, etc.
产品提示
Since applications vary, each investigator should titrate the reagent to obtain optimal results., Please refer to www.bdbiosciences.com/us/s/resources for technical protocols., Caution: Sodium azide yields highly toxic hydrazoic acid under acidic conditions. Dilute azide compounds in running water before discarding to avoid accumulation of potentially explosive deposits in plumbing., Source of all serum proteins is from USDA inspected abattoirs located in the United States.
背景信息
Maturation and post-translational modification of proteins occurs after their biosynthesis at the endoplasmic reticulum and their transport through the Golgi apparatus. The process involves the transport of vesicles carrying the proteins through a vectorial process of vesicle budding and fusion from the cis- compartment to the medial -compartment and the trans -compartment of the Golgi apparatus. The detergent insoluble fraction of the Golgi is named "matrix" and is required for proper morphology of the Golgi membranes. GM130 (Golgi matrix protein of 130 kDa) is a protein isolated from the Triton™ X-100-insoluble Golgi matrix and peripherally associated with the cis -compartment, as demonstrated by co-localization with syntaxin5. GM130 is homologous to the Golgi autoantigen golgin 95. GM130 interacts through its N-terminal domain with p115 and with the Golgi membranes at the C-terminal portion. Furthermore, the mitotic phosphorylation of GM130 blocks the interaction with p115. Thus, GM130 appears to function as a structural element of the Golgi apparatus that also provides attachment sites for membranes and other Golgi proteins. The 35/GM130 monoclonal antibody recognizes GM130, regardless of phosphorylation status.
文献引用 (375)
Autophagy dictates PHGDH-mediated serine metabolism in a timely manner to support oocyte development.
自噬及时调控PHGDH介导的丝氨酸代谢,以支持卵母细胞发育。
A missing enzyme-rescue metabolite as cause of a rare skeletal dysplasia
缺失的酶拯救代谢物是导致罕见骨骼发育不良的原因
ArfGAP2 promotes STING proton channel activity, cytokine transit, and autoinflammation
ArfGAP2促进STING质子通道活性、细胞因子转运和自身炎症
Elucidating subcellular architecture and dynamics at isotropic 100-nm resolution with 4Pi-SIM
利用4Pi-SIM以各向同性100纳米分辨率阐明亚细胞结构和动态
Muscle-derived miR-126 regulates TDP-43 axonal local synthesis and NMJ integrity in ALS models.
肌肉来源的 miR-126 调节 ALS 模型中 TDP-43 轴突局部合成和 NMJ 完整性。
Mitochondria are positioned at dendritic branch induction sites, a process requiring rhotekin2 and syndapin I.
线粒体位于树突分支诱导位点,这一过程需要 rhotekin2 和 syndapin I
Therapy-induced senescent cancer cells contribute to cancer progression by promoting ribophorin 1-dependent PD-L1 upregulation
治疗诱导的衰老癌细胞通过促进核糖体蛋白1依赖的PD-L1上调,促进癌症进展。
FUT10 and FUT11 are protein O-fucosyltransferases that modify protein EMI domains.
FUT10 和 FUT11 是蛋白质 O-岩藻糖基转移酶,可修饰蛋白质 EMI 结构域
ATG9A and ARFIP2 cooperate to control PI4P levels for lysosomal repair
ATG9A 和 ARFIP2 协同作用,控制溶酶体修复所需的 PI4P 水平。
Direct specification of lymphatic endothelium from mesenchymal progenitors
淋巴管内皮细胞直接由间充质祖细胞分化而来
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