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Rabbit Anti-SPATA15/SPATC1/PE-Cy5 Conjugated antibody (bs-17636R-PE-Cy5)
訂購(gòu)熱線:400-901-9800
訂購(gòu)郵箱:sales@xucheq.com
訂購(gòu)QQ:  400-901-9800
技術(shù)支持:techsupport@xucheq.com
說(shuō) 明 書(shū): 100ul  
100ul/2980.00元
大包裝/詢價(jià)
產(chǎn)品編號(hào) bs-17636R-PE-Cy5
英文名稱1 Rabbit Anti-SPATA15/SPATC1/PE-Cy5 Conjugated antibody
中文名稱 PE-Cy5標(biāo)記的精子發(fā)生相關(guān)蛋白15抗體
別    名 1700084J23Rik; MGC144830; MGC61633; SPATA15; Spatc1; SPERI_HUMAN; Speriolin; Spermatogenesis and centriole associated 1; Spermatogenesis and centriole-associated protein 1; Spermatogenesis-associated protein 15; Spermatogenic cell specific Cdc20 binding protein; Spermatogenic cell-specific Cdc20-binding protein.  
規(guī)格價(jià)格 100ul/2980元 購(gòu)買(mǎi)        大包裝/詢價(jià)
說(shuō) 明 書(shū) 100ul  
研究領(lǐng)域 細(xì)胞生物  發(fā)育生物學(xué)  細(xì)胞骨架  
抗體來(lái)源 Rabbit
克隆類(lèi)型 Polyclonal
交叉反應(yīng) Mouse,  (predicted: Human, Rat, Cow, Horse, Rabbit, Sheep, )
產(chǎn)品應(yīng)用 ICC=1:50-200 IF=1:50-200 
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
分 子 量 62kDa
性    狀 Lyophilized or Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human SPATA15/SPATC1
亞    型 IgG
純化方法 affinity purified by Protein A
儲(chǔ) 存 液 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
保存條件 Store at -20 °C for one year. Avoid repeated freeze/thaw cycles. The lyophilized antibody is stable at room temperature for at least one month and for greater than a year when kept at -20°C. When reconstituted in sterile pH 7.4 0.01M PBS or diluent of antibody the antibody is stable for at least two weeks at 2-4 °C.
產(chǎn)品介紹 background:
SPATA15 is a 591 amino acid cytoplasmic protein expressed in testis that is part of a complex that includes p55 CDC, Cdc27. The gene encoding Speriolin is located on human chromosome 8, which consists of nearly 146 million base pairs, houses more than 800 genes and is associated with a variety of diseases and malignancies. Schizophrenia, bipolar disorder, Trisomy 8, Pfeiffer syndrome, congenital hypothyroidism, Waardenburg syndrome and some leukemias and lymphomas are thought to occur as a result of defects in specific genes that map to chromosome 8.

Subunit:
Found in a complex with CDC20, CDC27 and TUBG1. Interacts with CDC20 (By similarity).

Subcellular Location:
Cytoplasm. Cytoplasm > cytoskeleton > centrosome. Colocalizes with the centrosomal pericentrin protein PCNT1.

Tissue Specificity:
Detected only in testis.

Database links:

Entrez Gene: 375686 Human

Entrez Gene: 74281 Mouse

Omim: 610874 Human

SwissProt: Q76KD6 Human

SwissProt: Q148B6 Mouse

Unigene: 97726 Human



Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
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