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RabbitAnti-SPIRE2 Rabbit pAb  antibody (bs-17678R)
~~~促销,代码KXJ230206~~~
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说明书: 50ul  100ul  200ul
50ul/1180.00元
100ul/1980.00元
200ul/2800.00元
大包装/询价

产品编号 bs-17678R
英文名称 SPIRE2 Rabbit pAb
中文名称 SPIRE2蛋白抗体
别    名 MGC117166; Protein spire homolog 2; Spir-2; SPIR2_HUMAN; Spire homolog 2(Drosophila); SPIRE2.  
Specific References  (1)     |     bs-17678R has been referenced in 1 publications.
111 [IF=5.413] Wang HH et al. Rab23/Kif17 regulate oocyte meiotic progression by modulating tubulin acetylation and actin dynamics. Development. 2019 Feb 4;146(3).  WB ;  Mouse.  222
研究领域 肿瘤  细胞生物  神经生物学  信号转导  细胞骨架  
抗体来源 Rabbit
克隆类型 Polyclonal
交叉反应 Mouse,  (predicted: Human, Rat, Chicken, Dog, Pig, Cow, Horse, Rabbit, Sheep, )
产品应用 WB=1:500-2000 ELISA=1:5000-10000 
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
理论分子量 80 kDa
检测分子量
细胞定位 细胞浆 
性    状 Liquid
浓    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human SPIRE2: 231-330/714 
亚    型 IgG
纯化方法 affinity purified by Protein A
缓 冲 液 0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.
保存条件 Shipped at 4℃. Store at -20℃ for one year. Avoid repeated freeze/thaw cycles.
注意事项 This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
PubMed PubMed
产品介绍 Spir-2 is a 714 amino acid protein belonging to the spire family. Spir-2 is a cytoplasmic protein that contains one KIND domain and three WH2 domains. Spir-2 binds to actin via the WH2 domains and acts as an actin nucleation factor. Spir-2 is involved in vesicle transport and acts as a link between actin organization and intracellular transport. Spir-2 is expressed as four isoforms that are produced by alternative splicing events. The gene that encodes Spir-2 maps to human chromosome 16, which encodes over 900 genes and approximately 90 million base pairs, making up nearly 3% of human cellular DNA. The GAN gene is located on chromosome 16 and, with mutation, may lead to giant axonal neuropathy, a nervous system disorder characterized by increasing malfunction with growth. The rare disorder Rubinstein-Taybi syndrome is also associated with chromosome 16, though through the CREBBP gene which encodes a critical CREB binding protein. Signs of Rubinstein-Taybi include mental retardation and predisposition to tumor growth and white blood cell neoplasias. Crohn's disease is a gastrointestinal inflammatory condition associated with chromosome 16 through the NOD2 gene.

Function:
Acts as a actin nucleation factor, remains associated with the slow-growing pointed end of the new filament. Involved in vesicle transport processes providing a novel link between actin organization and intracellular transport.

Subcellular Location:
Cytoplasm > cytoskeleton.

Similarity:
Belongs to the spire family.
Contains 1 KIND domain.
Contains 3 WH2 domains.

SWISS:
Q8WWL2

Gene ID:
84501

Database links:

Entrez Gene: 84501 Human

Entrez Gene: 234857 Mouse

Entrez Gene: 307925 Rat

Omim: 609217 Human

SwissProt: Q8WWL2 Human

SwissProt: Q8K1S6 Mouse

Unigene: 461786 Human



产品图片
Sample: Liver (Mouse) Lysate at 40 ug Primary: Anti-SPIRE2 (bs-17678R) at 1/300 dilution Secondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilution Predicted band size: 80 kD Observed band size: 80 kD
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