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    FUT4 Mouse mAb (bsm-33111M)  
    訂購熱線(xiàn):400-901-9800
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    訂購QQ:  400-901-9800
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    50ul/1180.00元
    100ul/1980.00元
    200ul/2800.00元
    200ug(PBS only)/5600.00元
    大包裝/詢(xún)價(jià)

    產(chǎn)品編號 bsm-33111M
    英文名稱(chēng) FUT4 Mouse mAb
    中文名稱(chēng) α-(1,3)-巖藻糖基轉移酶 4單克隆抗體
    別    名 FUT4_HUMAN; alpha-(1, 3)-fucosyltransferase 4; 4-galactosyl-N-acetylglucosaminide 3-alpha-L-fucosyltransferase; EC:2.4.1.152; ELAM-1 ligand fucosyltransferase; Fucosyltransferase 4; Fucosyltransferase IV(Fuc-TIV; FucT-IV); Galactoside 3-L-fucosyltransferase; ELFT; FCT3A; LeX; CD15; FUTIV; SSEA-1; SSEA1; FUC-TIV;  
    研究領(lǐng)域 腫瘤  細胞生物  免疫學(xué)  細胞膜受體  
    抗體來(lái)源 Mouse
    克隆類(lèi)型 Monoclonal
    克 隆 號 8B9
    交叉反應 Human,Mouse,Rat
    產(chǎn)品應用 IHC-P=1:200-1000,IHC-F=1:200-1000,IF=1:200-1000,Flow-Cyt=1ug/Test,ICC/IF=1:50-200
    not yet tested in other applications.
    optimal dilutions/concentrations should be determined by the end user.
    理論分子量 58 kDa
    檢測分子量
    細胞定位 細胞膜 
    性    狀 Liquid
    濃    度 1mg/ml
    免 疫 原 KLH conjugated synthetic peptide derived from human FUT4 
    亞    型 IgG
    純化方法 affinity purified by Protein G
    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 The Lewis histo-blood group system comprises a set of fucosylated glycosphingolipids that are synthesized by exocrine epithelial cells and circulate in body fluids. The glycosphingolipids function in embryogenesis, tissue differentiation, tumor metastasis, inflammation, and bacterial adhesion. They are secondarily absorbed to red blood cells giving rise to their Lewis phenotype. This gene is a member of the fucosyltransferase family, which catalyzes the addition of fucose to precursor polysaccharides in the last step of Lewis antigen biosynthesis. It encodes an enzyme with alpha(1,3)-fucosyltransferase and alpha(1,4)-fucosyltransferase activities. Mutations in this gene are responsible for the majority of Lewis antigen-negative phenotypes. Multiple alternatively spliced variants, encoding the same protein, have been found for this gene. [provided by RefSeq].

    Function:
    May catalyze alpha-1,3 glycosidic linkages involved in the expression of Lewis X/SSEA-1 and VIM-2 antigens.

    Subcellular Location:
    Golgi apparatus, Golgi stack membrane; Single-pass type II membrane protein. Note=Membrane-bound form in trans cisternae of Golgi.

    Tissue Specificity:
    Highest expression in stomach and colon. It is also expressed in the lung, testis, uterus, small intestine and to a lesser extent in spleen, and ovary. Present in trace amounts in brain, thymus, heart, smooth muscle, kidney and bone marrow. Not found in liver, salivary gland and pancreas.

    Similarity:
    Belongs to the glycosyltransferase 10 family.

    SWISS:
    P22083

    Gene ID:
    2526

    Database links:

    Entrez Gene: 10690 Human

    Entrez Gene: 2526 Human

    Entrez Gene: 2527 Human

    Entrez Gene: 2528 Human

    Entrez Gene: 2529 Human

    Omim: 104230 Human

    SwissProt: P22083 Human

    SwissProt: P51993 Human

    SwissProt: Q11128 Human

    SwissProt: Q11130 Human

    SwissProt: Q9Y231 Human

    Unigene: 390420 Human

    Unigene: 457 Human

    Unigene: 49117 Human

    Unigene: 572064 Human

    Unigene: 623098 Human

    Unigene: 631843 Human

    Unigene: 631846 Human

    Unigene: 705615 Human



    FUT4,也稱(chēng)為 ELFT 和 FCT3A,屬于糖基轉移酶 10 家族。FUT4 可催化參與 Lewis X/SSEA-1 和 VIM-2 抗原表達的 alpha-1,3 糖苷鍵。FUT4 是一種抗原表位,定義為 Lewis X 碳水化合物結構,在鼠胚胎癌細胞 (EC)、鼠 ES 和 iPS 細胞以及鼠和人類(lèi)生殖細胞上表達。它被廣泛用作小鼠未分化 ES 和 iPS 細胞的陽(yáng)性表面標志物和人未分化 ES 和 iPS 細胞的陰性表面標志物。
    產(chǎn)品圖片
    Paraformaldehyde-fixed, paraffin embedded Human Endometrial Cancer; Antigen retrieval by boiling in sodium citrate buffer (pH6.0) for 15 min; The section was incubated with FUT4 Monoclonal Antibody, Unconjugated (ascites of bsm-33111M) at 1:800 overnight at 4°C, followed by conjugation to the bs-40296G-HRP and DAB (C-0010) staining.
    Paraformaldehyde-fixed, paraffin embedded Human Kidney; Antigen retrieval by boiling in sodium citrate buffer (pH6.0) for 15 min; The section was incubated with FUT4 Monoclonal Antibody, Unconjugated (ascites of bsm-33111M) at 1:800 overnight at 4°C, followed by conjugation to the bs-40296G-HRP and DAB (C-0010) staining.
    Paraformaldehyde-fixed, paraffin embedded Human Spleen; Antigen retrieval by boiling in sodium citrate buffer (pH6.0) for 15 min; The section was incubated with FUT4 Monoclonal Antibody, Unconjugated (ascites of bsm-33111M) at 1:800 overnight at 4°C, followed by conjugation to the bs-40296G-HRP and DAB (C-0010) staining.
    Paraformaldehyde-fixed, paraffin embedded Human Lymph; Antigen retrieval by boiling in sodium citrate buffer (pH6.0) for 15 min; The section was incubated with FUT4 Monoclonal Antibody, Unconjugated (ascites of bsm-33111M) at 1:800 overnight at 4°C, followed by conjugation to the bs-40296G-HRP and DAB (C-0010) staining.
    Paraformaldehyde-fixed, paraffin embedded Human Colon Cancer; Antigen retrieval by boiling in sodium citrate buffer (pH6.0) for 15 min; The section was incubated with FUT4 Monoclonal Antibody, Unconjugated (ascites of bsm-33111M) at 1:800 overnight at 4°C, followed by conjugation to the bs-40296G-HRP and DAB (C-0010) staining.
    Paraformaldehyde-fixed, paraffin embedded Human Cervical Cancer; Antigen retrieval by boiling in sodium citrate buffer (pH6.0) for 15 min; The section was incubated with FUT4 Monoclonal Antibody, Unconjugated (ascites of bsm-33111M) at 1:800 overnight at 4°C, followed by conjugation to the bs-40296G-HRP and DAB (C-0010) staining.
    Paraformaldehyde-fixed, paraffin embedded Human Lung Cancer; Antigen retrieval by boiling in sodium citrate buffer (pH6.0) for 15 min; The section was incubated with FUT4 Monoclonal Antibody, Unconjugated (ascites of bsm-33111M) at 1:800 overnight at 4°C, followed by conjugation to the bs-40296G-HRP and DAB (C-0010) staining.
    Paraformaldehyde-fixed, paraffin embedded Human Kidney; Antigen retrieval by boiling in sodium citrate buffer (pH6.0) for 15 min; The section was incubated with FUT4 Monoclonal Antibody, Unconjugated (ascites of bsm-33111M) at 1:800 overnight at 4°C, followed by conjugation to the bs-40296G-HRP and DAB (C-0010) staining.
    Paraformaldehyde-fixed, paraffin embedded Human Breast Cancer; Antigen retrieval by boiling in sodium citrate buffer (pH6.0) for 15 min; The section was incubated with FUT4 Monoclonal Antibody, Unconjugated (bsm-33111M) at 1:200 overnight at 4°C, followed by conjugation to the bs-40296G-HRP and DAB (C-0010) staining.
    Paraformaldehyde-fixed, paraffin embedded Human Placenta; Antigen retrieval by boiling in sodium citrate buffer (pH6.0) for 15 min; The section was incubated with FUT4 Monoclonal Antibody, Unconjugated (bsm-33111M) at 1:200 overnight at 4°C, followed by conjugation to the bs-40296G-HRP and DAB (C-0010) staining.
    Paraformaldehyde-fixed, paraffin embedded Rat Kidney; Antigen retrieval by boiling in sodium citrate buffer (pH6.0) for 15 min; The section was incubated with FUT4 Monoclonal Antibody, Unconjugated (ascites of bsm-33111M) at 1:800 overnight at 4°C, followed by conjugation to the bs-40296G-HRP and DAB (C-0010) staining.
    Paraformaldehyde-fixed, paraffin embedded Mouse Kidney; Antigen retrieval by boiling in sodium citrate buffer (pH6.0) for 15 min; The section was incubated with FUT4 Monoclonal Antibody, Unconjugated (ascites of bsm-33111M) at 1:800 overnight at 4°C, followed by conjugation to the bs-40296G-HRP and DAB (C-0010) staining.
    Paraformaldehyde-fixed, paraffin embedded Human Cerebrum; Antigen retrieval by boiling in sodium citrate buffer (pH6.0) for 15 min; The section was incubated with FUT4 Monoclonal Antibody, Unconjugated (ascites of bsm-33111M) at 1:200 overnight at 4°C, followed by conjugation to the bs-40296G-HRP and DAB (C-0010) staining.
    Paraformaldehyde-fixed, paraffin embedded Rat Cerebrum; Antigen retrieval by boiling in sodium citrate buffer (pH6.0) for 15 min; The section was incubated with FUT4 Monoclonal Antibody, Unconjugated (ascites of bsm-33111M) at 1:200 overnight at 4°C, followed by conjugation to the bs-40296G-HRP and DAB (C-0010) staining.
    Paraformaldehyde-fixed, paraffin embedded Mouse Cerebrum; Antigen retrieval by boiling in sodium citrate buffer (pH6.0) for 15 min; The section was incubated with FUT4 Monoclonal Antibody, Unconjugated (ascites of bsm-33111M) at 1:200 overnight at 4°C, followed by conjugation to the bs-40296G-HRP and DAB (C-0010) staining.
    4% Paraformaldehyde-fixed THP-1 (H) cell; Triton X-100 at r.t. for 20 min; Antibody incubation with (FUT4) monoclonal Antibody, unconjugated (bsm-33111M) 1:100, 90 min at 37°C; followed by conjugated Goat Anti-Mouse IgG antibody (green, bs-60296G-FITC) at 37°C for 90 min, DAPI (blue, C02-04002) was used to stain the cell nuclei. PBS instead of the primary antibody was used as the blank control.
    The THP-1 (H) cells were fixed with 4% PFA (10 min at r.t.) and then permeabilized with 90% ice-cold methanol for 20 min at -20℃,the cells then were incubated in 5%BSA to block non-specific protein-protein interactions (30 min at r.t.).Primary Antibody (green):Mouse Anti-FUT4 antibody (bsm-33111M): 1 μg/10^6 cells; Secondary Antibody (white blue): Goat anti-Mouse IgG-FITC (bs-60296G-FITC): 1 μg/test. Blank control (black): PBS. Acquisition of 20,000 events was performed.
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