产品介绍 FAQs 评论(0)
宿主来源
Rat抗原名称
GBP1分子别名
Guanylate-binding protein 1; GTP-binding protein 1; GBP-1; HuGBP-1; hGBP1; Guanine nucleotide-binding protein 1; Interferon-induced guanylate-binding protein 1细胞定位
Golgi apparatus membrane, Cytoplasm, Secreted, Cell membraneAccession
P32455克隆号
S-R186抗体类型
Rat mAb抗体同种型
IgG1反应种属 ?
Hu纯化方式
Protein G浓度
2 mg/ml标记
Unconjugated性状
Liquid缓冲体系
PBS, 40% Glycerol, 0.05% BSA, 0.03% Proclin 300
储存条件
12 months from date of receipt / reconstitution, -20 °C as supplied
应用
IHC-P ?
ICC ?
WB
IP
稀释度
应用 稀释度 WB 1:1000 IP 1:50 IHC 1:100 ICC 1:500
A single cluster of seven human GBP genes (GBP1-GBP7) is found on chromosome 1q22.2. Human GBP1 is secreted from cells without the need of a leader peptide, and has been shown to exhibit antiviral activity against Vesicular stomatitis virus and Encephalomyocarditis virus, as well as being able to regulate the inhibition of proliferation and invasion of endothelial cells in response to IFN-gamma [PMID: 16936281].
免疫印迹
WB result of GBP1 Rat mAb
Primary antibody: GBP1 Rat mAb at 1/1000 dilution
Lane 1: HeLa whole cell lysate 20 µg
Lane 2: HeLa treated with IFN-γ (50 ng/ml 16 hr) whole cell lysate 20 µg
Lane 3: Jurkat whole cell lysate 20 µg
Secondary antibody: Goat Anti-Rat IgG, (H+L), HRP conjugated at 1/10000 dilution
Predicted MW: 68 kDa
Observed MW: 68 kDa
Exposure time: 20 s
免疫沉淀
GBP1 Rat mAb at 1/200 dilution (1 µg) immunoprecipitating GBP1 in 0.4 mg Jurkat whole cell lysate.
Western blot was performed on the immunoprecipitate using GBP1 Rat mAb at 1/1000 dilution.
Goat Anti-Rat IgG, (H+L), HRP conjugated at 1/10000 dilution.
Lane 1: Jurkat whole cell lysate 20 µg (Input)
Lane 2: GBP1 Rat mAb IP in Jurkat whole cell lysate
Lane 3: Rat monoclonal IgG1 IP in Jurkat whole cell lysate
Predicted MW: 68 kDa
Observed MW: 68 kDa
免疫组化
IHC shows positive staining in paraffin-embedded human tonsil. Anti-GBP1 antibody was used at 1/100 dilution, followed by a Goat Anti-Rat IgG (H+L). Counterstained with hematoxylin. Heat mediated antigen retrieval with Tris/EDTA buffer pH9.0 was performed before commencing with IHC staining protocol.
IHC shows positive staining in paraffin-embedded human spleen. Anti-GBP1 antibody was used at 1/100 dilution, followed by a Goat Anti-Rat IgG (H+L). Counterstained with hematoxylin. Heat mediated antigen retrieval with Tris/EDTA buffer pH9.0 was performed before commencing with IHC staining protocol.
免疫细胞化学
ICC analysis of HeLa cells treated with IFNγ (50ng/ml, 16h) (top panel) and untreated HeLa cells (below panel). Anti- GBP1 antibody was used at 1/500 dilution (Green) and incubated overnight at 4°C. Goat polyclonal Antibody to Rabbit IgG - H&L (Alexa Fluor® 488) was used as secondary antibody at 1/1000 dilution. The cells were fixed with 100% ice-cold methanol and permeabilized with 0.1% PBS-Triton X-100. Nuclei were counterstained with DAPI (Blue).
FAQs
我们一般不推荐客户回收利用抗体。 因为抗体使用之后缓冲体系已经发生改变,不同客户在回收抗体的保存条件上也会有差异,所以抗体回收使用效果无法保证。另外,我们对一批抗体回收验证测试,测试结果显示不同抗体可回收次数不同,一般效价越高的抗体,可重复使用的次数越多,客户可根据实验情况来确定







评论(0)