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WB 试剂
- PonceauS Staining Solution
- PBST Washing Buffer, 10X
- 1.5M Tris-HCl Buffer, pH8.8
- 1M Tris-HCl Buffer, pH6.8
- 10% SDS Solution
- Prestained Protein Marker
- TBST Washing Buffer, 10X
- SDS PAGE Loading Buffer, 5X
- Stripping Buffered Solution
- Tris Buffer, pH7.4, 10X
- Total Protein Extraction Kit
- Running Buffer, 10X
- Transfer Buffer, 10X
- 30% Acr-Bis(29:1) Solution
- Tris电泳液速溶颗粒
- PBS(1X, premixed powder)
- TBS(1X, premixed powder)
- 快速封闭液
- 转膜液速溶颗粒
- Chemical reagents
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GBP1 Polyclonal Antibody
- 货号:YT1867
- 应用:WB;IF;ELISA
- 种属:Human;Rat;Mouse;
- 简介:
- >>NOD-like receptor signaling pathway
- 蛋白名称:
- Interferon-induced guanylate-binding protein 1
- 免疫原:
- The antiserum was produced against synthesized peptide derived from human GBP1. AA range:71-120
- 特异性:
- GBP1 Polyclonal Antibody detects endogenous levels of GBP1 protein.
- 组成:
- Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
- 来源:
- Polyclonal, Rabbit,IgG
- 稀释:
- WB 1:500 - 1:2000. IF 1:200 - 1:1000. ELISA: 1:40000. Not yet tested in other applications.
- 纯化工艺:
- The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
- 储存:
- -15°C to -25°C/1 year(Do not lower than -25°C)
- 其他名称:
- GBP1;Interferon-induced guanylate-binding protein 1;GTP-binding protein 1;GBP-1;HuGBP-1;Guanine nucleotide-binding protein 1
- 背景:
- Guanylate binding protein expression is induced by interferon. Guanylate binding proteins are characterized by their ability to specifically bind guanine nucleotides (GMP, GDP, and GTP) and are distinguished from the GTP-binding proteins by the presence of 2 binding motifs rather than 3. [provided by RefSeq, Jul 2008],
- 功能:
- function:Binds GTP, GDP and GMP.,induction:By interferon gamma during macrophage activation.,similarity:Belongs to the GBP family.,
- 细胞定位:
- Cytoplasm . Golgi apparatus membrane; Lipid-anchor ; Cytoplasmic side. Cell membrane . Secreted . Cytoplasmic vesicle . Secreted from endothelial cells in the cerebrospinal fluid, upon bacterial challenge and independently of IFNG induction. Golgi membrane localization requires isoprenylation and the presence of another IFNG-induced factor.
- 组织表达:
- Placenta,Spleen,Uterus,
![](/uploadfiles/PIC/yt1867_pic621818522.jpg)
- Immunofluorescence analysis of MCF7 cells, using GBP1 Antibody. The picture on the right is blocked with the synthesized peptide.
![](/uploadfiles/PIC/yt1867_pic621918522.jpg)
- Western blot analysis of lysates from HUVEC cells, using GBP1 Antibody. The lane on the right is blocked with the synthesized peptide.