- 询价
- Cell Signaling Technology
- 8886
- USA
- 2025年12月20日
- W
- H,Mk,Hm
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- 详细信息
- 文献和实验
- 技术资料
- 抗体英文名：
PICH (D4G8) Rabbit mAb
- 抗原：
synthetic peptide corresponding to residues surrounding Gly610 of human PICH protein
- 应用范围：
W
- 级别：
详见MSDS文件
- 供应商：
CST
- 保质期：
详见说明书
- 适应物种：
H,Mk,Hm
- 库存：
大量
- 是否单克隆：
1
- 保存条件：
-20°c
- 规格：
100 ul (10 western blots)/carrier free & custom formulation / quantity
| 规格： | 产品价格： | ￥请询价 | |
|---|---|---|---|
| 规格： | 100 ul (10 western blots) | 产品价格： | ￥请询价 |
| 规格： | carrier free & custom formulation / quantity | 产品价格： | ￥请询价 |
pathway more info application references datasheet PDF MSDS PDF protocols
Applications Key: W=Western Blotting
Reactivity Key: H=Human Hm=Hamster Mk=Monkey
Species cross-reactivity is determined by western blot. Species enclosed in parentheses are predicted to react based on 100% sequence homology.
| Applications | Reactivity | Sensitivity | MW (kDa) | Isotype |
|---|---|---|---|---|
| W | H Mk (Hm) | Endogenous | 175 | Rabbit IgG |
| Protocols |
|
|---|---|
| Specificity / Sensitivity | PICH (D4G8) Rabbit mAb recognizes endogenous levels of total PICH protein. |
| Source / Purification | Monoclonal antibody is produced by immunizing animals with a synthetic peptide corresponding to residues surrounding Gly610 of human PICH protein. Western Blotting
Western blot analysis of extracts from various cell lines using PICH (D4G8) Rabbit mAb. |
| Background | PICH is a helicase of the SNF2 family of ATPases and is essential for proper chromosome segregation during mitosis (1). While PICH was originally proposed to participate in spindle assembly checkpoint signaling (1), that function was subsequently called into question (2). When phosphorylated at Thr1063 by CDK1, PICH binds the polo-box domain of the mitotic kinase PLK1 (1) and targets it to chromosome arms (3), where it appears to facilitate proper chromosome arm cohesion (4). PICH is also a substrate of PLK1 (1). Localized to the cytoplasm during interphase, PICH begins to accumulate at centromeres and kinetochores in prometaphase (4). As chromosomes begin to separate at the onset of anaphase, PICH associates with ultrafine threads between sister centromeres thought to be composed of entangled DNA (5), a natural consequence of DNA replication. PICH is proposed to cooperate with BLM, a RecQ-like helicase implicated in the genetic disorder Bloom’s Syndrome, to displace centromeric histones along these threads, thus enabling them to span large distances without breaking (6). This provides a temporal window for topoisomerase IIα-mediated disentanglement (7). Defects in PICH or BLM disrupt proper chromatid segregation and result in the formation of micronuclei (6).
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| Application References | Have you published research involving the use of our products? If so we'd love to hear about it. Please let us know ! |
| Companion Products |
For Research Use Only. Not For Use In Diagnostic Procedures. |
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文献和实验Methods for the Detection of D-Amino-Acid Oxidase
then twice for 5 min. It was incubated for 1 hr in TBS-T containing rabbit anti-hog D-amino-acid oxidase IgG (1/3,000 dilution) and quickly rinsed twice with TBS-T and further washed in TBS-T once for 15 min then twice for 5 min. The membrane was incubated
组织化学分析。（图 C）使用Anti-Erk1/2 Mouse mAb 鼠单抗进行目的蛋白检测；(图 D) 使用p44/42 MAPK （Erk1/2）Rabbit mAb 兔单抗进行目的蛋白检测。 图 7 免疫组化实验检测Akt表达 注：使用 Anti-Akt (pan) Rabbit mAb 对正常小鼠肝组织进行免疫组织化学分析。（图 E）使用免疫组化试剂盒 M&R HRP/DAB Detection IHC Kit，抗体1:100 稀释；(图F)使用另一种试剂盒，抗体 1:100 稀释。
Methods for the Detection of D-Amino-Acid Oxidase
min then twice for 5 min. It was incubated for 1 hr in TBS-T containing rabbit anti-hog D-amino-acid oxidase IgG (1/3,000 dilution) and quickly rinsed twice with TBS-T and further washed in TBS-T once for 15 min then twice for 5 min. The membrane
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