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IHC

Nucleophosmin (ABT210) Mouse mAb (Ready to Use)

-YM6898R

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主要信息
Target

Nucleophosmin

Host Species

Mouse

Reactivity

Human

Applications

IHC

Conjugate/Modification

Unmodified

货号: YM6898R
规格
价格
货期
数量
10mL
¥1,200.00
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0

6mL
¥900.00
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3mL
¥600.00
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详细信息
推荐稀释比
Ready to use for IHC
组成
The prediluted ready-to-use antibody is diluted in phosphate buffer saline containing stabilizing protein and 0.05% Proclin 300
特异性
The antibody can specifically recognize human Nucleophosmin protein.
纯化工艺
The antibody was affinity-purified from ascites by affinity-chromatography using specific immunogen.
储存
2°C to 8°C/1 year,Ship by ice bag
修饰
Unmodified
克隆性
Monoclonal
克隆号
ABT210
同种型
IgG2b, Kappa
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抗原&靶点信息
免疫原:
Synthesized peptide derived from human Nucleophosmin AA range: 100-200
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特异性:
The antibody can specifically recognize human Nucleophosmin protein.
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基因名称:
NPM1 NPM
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蛋白名称:
Nucleophosmin
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别名:
NPM1 ;
NPM ;
Nucleophosmin ;
NPM ;
Nucleolar phosphoprotein B23 ;
Nucleolar protein NO38 ;
Numatrin
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数据库链接:
Organism 基因 ID SwissProt
Human 4869; P06748;
背景:
This gene encodes a phosphoprotein which moves between the nucleus and the cytoplasm. The gene product is thought to be involved in several processes including regulation of the ARF/p53 pathway. A number of genes are fusion partners have been characterized , in particular the anaplastic lymphoma kinase gene on chromosome 2. Mutations in this gene are associated with acute myeloid leukemia. More than a dozen pseudogenes of this gene have been identified. Alternative splicing results in multiple transcript variants.[provided by RefSeq , Nov 2009] ,
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功能:
Disease:A chromosomal aberration involving NPM1 is a cause of myelodysplastic syndrome (MDS) . Translocation t (3;5) (q25.1;q34) with MLF1. ,Disease:A chromosomal aberration involving NPM1 is found in a form of acute promyelocytic leukemia. Translocation t (5;17) (q32;q11) with RARA. ,Disease:A chromosomal aberration involving NPM1 is found in a form of non-Hodgkin lymphoma. Translocation t (2;5) (p23;q35) with ALK. The resulting chimeric NPM1-ALK protein homodimerize and the kinase becomes constitutively activated. ,Disease:Defects in NPM1 are associated with acute myelogenous leukemia (AML) . Mutations in exon 12 affecting the C-terminus of the protein are associated with an aberrant cytoplasmic location. ,Function:Involved in diverse cellular processes such as ribosome biogenesis , centrosome duplication , protein chaperoning , histone assembly , cell proliferation , and regulation of tumor suppressors TP53/p53 and ARF. Binds ribosome presumably to drive ribosome nuclear export. Associated with nucleolar ribonucleoprotein structures and bind single-stranded nucleic acids. Acts as a chaperonin for the core histones H3 , H2B and H4. ,PTM:Acetylated at C-terminal lysine residues , thereby increasing affinity to histones. ,PTM:ADP-ribosylated. ,PTM:Phosphorylated at Ser-4 by PLK1. Phosphorylated by CDK2 at Ser-125 and Thr-199. Phosphorylation at Thr-199 may trigger initiation of centrosome duplication. Phosphorylated by CDC2 at Thr-199 , Thr-219 , Thr-234 and Thr-237 during cell mitosis. When these four sites are phosphorated , RNA-binding activity seem to be abolished. May be phosphoryled at Ser-70 by NEK2. ,PTM:Sumoylated by ARF. ,similarity:Belongs to the nucleoplasmin family. ,subcellular location:Generally nucleolar , but is translocated to the nucleoplasm in case of serum starvation or treatment with anticancer drugs. Has been found in the cytoplasm in patients with primary acute myelogenous leukemia (AML) , but not with secondary AML. Can shuttle between cytoplasm and nucleus. ,subunit:Decamer formed by two pentameric rings associated in a head-to-head fashion. Disulfide-linked dimers under certain conditions. The SWAP complex consists of NPM1 , NCL , PARP1 and SWAP70 (By similarity) . Interacts with NSUN2. Interacts with hepatitis delta virus S-HDAg. ,
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细胞定位:
Nuclear , Cytoplasmic
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组织表达:
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货号: YM6898R
规格
价格
货期
数量
10mL
¥1,200.00
现货

0

6mL
¥900.00
现货

0

3mL
¥600.00
现货

0

加入购物车

已收藏

收藏

定制服务咨询
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