- $495
- Leading Biology
- United States
- APR12672G
- 2025年09月13日
- Rabbit
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- 文献和实验
- 技术资料
- 保存条件：
Store at +4°C short term. For long-term storage, aliquot and store at -20°C or below. Stable for 12 months at -20°C. Avoid repeated freeze-thaw cycles.
- 库存：
100
- 宿主：
Rabbit
- 靶点：
Human P2RY12 / P2Y12. BLAST analysis of the peptide immunogen showed no homology with other human proteins, except CACNA1F (56%).
- 抗体名：
HORK3
- 规格：
50 μg
39kDa
细胞定位：
Antigen Cellular Localization: Cell membrane; Multi-pass membrane protein
形式：
Liquid
参考文献：
Hollopeter G.,et al.Nature 409:202-207(2001). Zhang F.L.,et al.J. Biol. Chem. 276:8608-8615(2001). Takasaki J.,et al.Mol. Pharmacol. 60:432-439(2001). Reinscheid R.K.,et al.Submitted (OCT-2000) to the EMBL/GenBank/DDBJ databases. Bruess M.,et al.Submitted (AUG-2002) to the EMBL/GenBank/DDBJ databases.
产品概述：
We constantly strive to ensure we provide our customers with the best antibodies. As a result of this work we offer this antibody in purified format. We are in the process of updating our datasheets. If you have any questions regarding this update, please feel free to contact our technical support team. This product is a high quality P2RY12 / P2Y12 antibody (Extracellular Domain).
功能：
Receptor for ADP and ATP coupled to G-proteins that inhibit the adenylyl cyclase second messenger system. Not activated by UDP and UTP. Required for normal platelet aggregation and blood coagulation.
总结：
Receptor for ADP and ATP coupled to G-proteins that inhibit the adenylyl cyclase second messenger system. Not activated by UDP and UTP. Required for normal platelet aggregation and blood coagulation.
联系方式：
生物商城：http://www.annoron.com
办公电话：010-56256916
官方售后：400-965-8633
企业 QQ：3212874516、3198592576
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文献和实验secondary antibody review -- data from 99 publications
cytometry used as a control to detect cell responses targeted antigen 7 Alexa Fluor 488 7 Cy3 8 goat IgG Alexa Fluor 488 1:2000 detect antibody binding in human embryonic kidney 293T cells Invitrogen 9 donkey
Quantitative immunoprecipitation of GFP-fusion proteins using the GFP-Trap
) (Abcam, Cambridge, UK; Sigma, St. Louis, USA.; Roche, Mannheim, Germany). We recently generated a GFP-binding protein (GBP) based on a single domain antibody derived from Lama alpaca (Rothbauer et al., 2008). This GFP-binding protein is characterized
either induced the expression of an endothelial-specific differentiation marker, VE-cadherin, in non-endothelial cell lines or, when combined with a repression domain, knocked down expression. Potential binding sites for a number of these transcription factors
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