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Rabbit Anti-Musashi 1  antibody (bs-11201R)  
~~~促銷代碼KT202411~~~
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產品編號 bs-11201R
英文名稱 Rabbit Anti-Musashi 1  antibody
中文名稱 神經干細胞RNA結合蛋白Musashi1抗體
別    名 Musashi 1 / Msi1; Msi 1; Msi1; Msi-1; MSI1H_HUMAN; Musashi homolog 1; Musashi-1; Musashi1; RNA binding protein Musashi homolog 1; RNA-binding protein Musashi homolog 1.  
研究領域 腫瘤  神經生物學  干細胞  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應 Human,Mouse,Rat (predicted: Rabbit,Pig,Cow,Chicken,Dog)
產品應用 IHC-P=1:100-500,IHC-F=1:100-500,Flow-Cyt=2ug/Test,ICC/IF=1:100,IF=1:100-500
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
理論分子量 39kDa
細胞定位 細胞核 細胞漿 
性    狀 Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human Musashi 1: 66-150/362 
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
產品介紹 Musashi1 (Msi1) is an RNA-binding protein expressed in neural progenitor cells and neural stem cells. Msi1 is the mammalian homolog of Drosophila Musashi. The gene encoding human Msi1 encodes a 362 amino acid protein. In murine embryonic neural progenitor cells, Msi1 localizes to the cytoplasm and is downregulated during differentiation. Msi1 binds to NUMB, which encodes a membrane-associated antagonist of Notch signaling. Msi1 appears to function in the proliferation and maintenance of stem cell populations of the central nervous system. In addition to its usefulness as a marker for neural progenitor cells in normal human brains, Msi1 is also a marker for human gliomas. In rats, Msi1 is expressed in Sertoli cells of the testis and granulosa cells of the ovary.

Function:
RNA binding protein that regulates the expression of target mRNAs at the translation level. Regulates expression of the NOTCH1 antagonist NUMB. Binds RNA containing the sequence 5'-GUUAGUUAGUUAGUU-3' and other sequences containing the pattern 5'-[GA]U(1-3)AGU-3'. May play a role in the proliferation and maintenance of stem cells in the central nervous system.

Subcellular Location:
Cytoplasm. Nucleus.

Tissue Specificity:
Detected in fetal kidney, brain, liver and lung, and in adult brain and pancreas. Detected in hepatoma cell lines.

Similarity:
Belongs to the Musashi family.
Contains 2 RRM (RNA recognition motif) domains.

SWISS:
O43347

Gene ID:
4440

Database links:

Entrez Gene: 4440 Human

Entrez Gene: 17690 Mouse

Entrez Gene: 259272 Rat

Omim: 603328 Human

SwissProt: O43347 Human

SwissProt: Q61474 Mouse

SwissProt: Q8K3P4 Rat

Unigene: 158311 Human

Unigene: 5077 Mouse

Unigene: 162146 Rat



Musashi1是一種進化保守的RNA結合蛋白,在維持干細胞狀態、分化和腫瘤發生方面起著重要作用。Musashi1 選擇性地表達在神經前體細胞上,包括神經干細胞上。在神經系統外,Musashi1還是腸干細胞的選擇性標記。這些組織干細胞或未成熟細胞Musashi1的表達,表明Musashi1在轉錄后基因調節階段維持這些細胞未分化狀態起重要作用。Musashi1過度表達通過依賴RBP2Jk的旁路激活Notch1,而Notch信號途徑功能為誘導哺乳動物神經干細胞自我更新。通過musashi1-P-小鼠培養腦細胞的Musashi蛋白產物反義去除研究,發現這些基因在維持神經干細胞未分化狀態起著重要的作用。 Musashi抑制m-Numb轉錄的分子機制尚待進一步研究。Musashi1有可能除轉錄調控外還參與其他調控途徑。另外,Musashi1還表達在一些腦腫瘤的特殊類型(這些腫瘤可能起源自非成熟腦細胞),并且表達水平和腫瘤的惡性程度及增殖能力相關。
產品圖片
Paraformaldehyde-fixed, paraffin embedded (rat pancreas); Antigen retrieval by boiling in sodium citrate buffer (pH6.0) for 15min; Block endogenous peroxidase by 3% hydrogen peroxide for 20 minutes; Blocking buffer (normal goat serum) at 37°C for 30min; Antibody incubation with (Musashi 1) Polyclonal Antibody, Unconjugated (bs-11201R) at 1:200 overnight at 4°C, followed by operating according to SP Kit(Rabbit) (sp-0023) instructionsand DAB staining.
Tissue/cell: mouse pancreas tissue; 4% Paraformaldehyde-fixed and paraffin-embedded; Antigen retrieval: citrate buffer ( 0.01M, pH 6.0 ), Boiling bathing for 15min; Block endogenous peroxidase by 3% Hydrogen peroxide for 30min; Blocking buffer (normal goat serum,C-0005) at 37℃ for 20 min; Incubation: Anti-Musashi-1 Polyclonal Antibody, Unconjugated(bs-11201R) 1:200, overnight at 4°C, followed by conjugation to the secondary antibody(SP-0023) and DAB(C-0010) staining
Tissue/cell: mouse brain tissue; 4% Paraformaldehyde-fixed and paraffin-embedded; Antigen retrieval: citrate buffer ( 0.01M, pH 6.0 ), Boiling bathing for 15min; Block endogenous peroxidase by 3% Hydrogen peroxide for 30min; Blocking buffer (normal goat serum,C-0005) at 37℃ for 20 min; Incubation: Anti-Musashi-1 Polyclonal Antibody, Unconjugated(bs-11201R) 1:200, overnight at 4°C, followed by conjugation to the secondary antibody(SP-0023) and DAB(C-0010) staining
SH-SY5Y cell; 4% Paraformaldehyde-fixed; Triton X-100 at room temperature for 20 min; Blocking buffer (normal goat serum, C-0005) at 37°C for 20 min; Antibody incubation with (Musashi 1) polyclonal Antibody, Unconjugated (bs-11201R) 1:100, 90 minutes at 37°C; followed by a conjugated Goat Anti-Rabbit IgG antibody at 37°C for 90 minutes, DAPI (blue, C02-04002) was used to stain the cell nuclei.
Blank control(black line):SH-SY5Y. Primary Antibody (green line): Rabbit Anti-Musashi 1 antibody (bs-11201R) Dilution:2ug/Test; Secondary Antibody(white blue line): Goat anti-rabbit IgG-AF488 Dilution: 0.5ug/Test. Isotype control(orange line): Normal Rabbit IgG Protocol The cells were fixed with 4% PFA (10min at room temperature)and then permeabilized with 90% ice-cold methanol for 20 min at -20℃, The cells were then incubated in 5%BSA to block non-specific protein-protein interactions for 30 min at room temperature .Cells stained with Primary Antibody for 30 min at room temperature. The secondary antibody used for 40 min at room temperature. Acquisition of 20,000 events was performed.
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