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    FLII Rabbit pAb (bs-7864R)  
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    產(chǎn)品編號 bs-7864R
    英文名稱(chēng) FLII Rabbit pAb
    中文名稱(chēng) 蛋白質(zhì)flightless-1同源物抗體
    別    名 Fli 1; FLI; Flightless-1; Flightless1; Flightless 1; Flightless I(Drosophila) homolog; Flightless I homolog; Flightless I homolog(Drosophila); Flightless1; FlightlessI; Fliih; MGC39265; Protein flightless 1 homolog; FLI1_HUMAN.  
    研究領(lǐng)域 細胞生物  免疫學(xué)  干細胞  細胞周期蛋白  細胞分化  細胞骨架  
    抗體來(lái)源 Rabbit
    克隆類(lèi)型 Polyclonal
    克 隆 號
    交叉反應 Mouse,Rat (predicted: Human,Rabbit,Pig,Cow,Chicken,Dog,Horse)
    產(chǎn)品應用 WB=1:500-2000,IHC-P=1:100-500,IHC-F=1:100-500,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 51 kDa
    檢測分子量
    細胞定位 細胞核 
    性    狀 Liquid
    濃    度 1mg/ml
    免 疫 原 KLH conjugated synthetic peptide derived from human Flightless 1: 343-452/452 
    亞    型
    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 This gene encodes a protein with a gelsolin-like actin binding domain and an N-terminal leucine-rich repeat-protein protein interaction domain. The protein is similar to a Drosophila protein involved in early embryogenesis and the structural organization of indirect flight muscle. The gene is located within the Smith-Magenis syndrome region on chromosome 17. Mutations in this gene leads to abnormal muscle function, arrested development and embryonic lethality. The protein sequence shows that this might be a regulator of cytoskeleton and may have a role during cell division.

    Function:
    Sequence-specific transcriptional activator. Recognizes the DNA sequence 5'-C[CA]GGAAGT-3'.

    Subunit:
    Can form homodimers or heterodimers with ETV6/TEL1.

    Subcellular Location:
    Nucleus.

    DISEASE:
    Defects in FLI1 are a cause of Ewing sarcoma (ES) [MIM:612219]. A highly malignant, metastatic, primitive small round cell tumor of bone and soft tissue that affects children and adolescents. It belongs to the Ewing sarcoma family of tumors, a group of morphologically heterogeneous neoplasms that share the same cytogenetic features. They are considered neural tumors derived from cells of the neural crest. Ewing sarcoma represents the less differentiated form of the tumors. Note=A chromosomal aberration involving FLI1 is found in patients with Erwing sarcoma. Translocation t(11;22)(q24;q12) with EWSR1.

    Similarity:
    Belongs to the ETS family. Contains 1 ETS DNA-binding domain. Contains 1 PNT (pointed) domain.

    SWISS:
    Q13045

    Gene ID:
    2314

    Database links:

    Entrez Gene: 2314 Human

    Entrez Gene: 14248 Mouse

    Entrez Gene: 287375 Rat

    Omim: 600362 Human

    SwissProt: Q13045 Human

    SwissProt: Q9JJ28 Mouse

    Unigene: 513984 Human

    Unigene: 339755 Mouse

    Unigene: 144698 Rat



    產(chǎn)品圖片
    Sample: Heart (Mouse) Lysate at 40 ug Primary: Anti- Flightless 1 (bs-7864R) at 1/1000 dilution Secondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilution Predicted band size: 51 kD Observed band size: 51 kD
    Paraformaldehyde-fixed, paraffin embedded (rat brain); 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 (Flightless 1) Polyclonal Antibody, Unconjugated (bs-7864R) at 1:200 overnight at 4°C, followed by operating according to SP Kit(Rabbit) (sp-0023) instructionsand DAB staining.
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