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SPIRE2 Rabbit pAb (bs-17678R)  
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產(chǎn)品編號 bs-17678R
英文名稱 SPIRE2 Rabbit pAb
中文名稱 SPIRE2蛋白抗體
別    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.
[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.  
研究領域 腫瘤  細胞生物  神經(jīng)生物學  信號轉導  細胞骨架  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應 Mouse (predicted: Human,Rat,Rabbit,Pig,Sheep,Cow,Chicken,Dog,Horse)
產(chǎn)品應用 WB=1:500-2000
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
理論分子量 80 kDa
檢測分子量
細胞定位 細胞漿 
性    狀 Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human SPIRE2: 231-330/714 
亞    型 IgG
純化方法 affinity purified by Protein A
緩 沖 液 0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.
保存條件 Shipped at 4℃. Store at -20℃ for one year. Avoid repeated freeze/thaw cycles.
注意事項 This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
PubMed PubMed
產(chǎn)品介紹 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



產(chǎn)品圖片
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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