BD Pharmingen™ Purified Mouse Anti-β-Tubulin
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BD Pharmingen™ Purified Mouse Anti-β-Tubulin

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品牌: BD Pharmingen
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    反应种属:
    Human (QC Testing), Mouse,Rat,Cow (Tested in Development)
    Human (QC Testing), Mouse,Rat,Cow (Tested in Development)
    来源宿主:
    Mouse IgM, κ
    Mouse IgM, κ
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    产品介绍
    产品信息
    抗原名称
    β-Tubulin
    宿主
    Mouse IgM, κ
    简单描述
    Tubulin is a highly conserved protein with a molecular weight of ~50 kD.  The self-assembly of tubulin leads to microtubules, hollow cylinders that are one of the major components of the eukaryotic cytoskeleton.  Microtubules play key roles in chromosome segregation in mitosis, intracellular transport, ciliary and flagellar bending, and structural support of the cytoskeleton.  There are two main classes of tubulin isoforms, α- and β-tubulin, which are usually products of separate genes.  Microtubules are made from protofilaments, strings of alternating α- and β-tubulin spaced 4 nm apart and pointing in the same direction.  Tubulin can be posttranslationally modified in several ways, including phosphorylation, acetylation, glutamylation, and detyrosination.  For example, microtubules that turn over slowly tend to be acetylated and detyrosinated. The 5H1 monoclonal antibody reacts with β-tubulin.  It does not cross-react with α-tubulin.
    商品描述
    5H1 Tubulin is a highly conserved protein with a molecular weight of ~50 kD.  The self-assembly of tubulin leads to microtubules, hollow cylinders that are one of the major components of the eukaryotic cytoskeleton.  Microtubules play key roles in chromosome segregation in mitosis, intracellular transport, ciliary and flagellar bending, and structural support of the cytoskeleton.  There are two main classes of tubulin isoforms, α- and β-tubulin, which are usually products of separate genes.  Microtubules are made from protofilaments, strings of alternating α- and β-tubulin spaced 4 nm apart and pointing in the same direction.  Tubulin can be posttranslationally modified in several ways, including phosphorylation, acetylation, glutamylation, and detyrosination.  For example, microtubules that turn over slowly tend to be acetylated and detyrosinated. The 5H1 monoclonal antibody reacts with β-tubulin.  It does not cross-react with α-tubulin.
    同种型
    Mouse IgM, κ
    克隆号
    克隆 5H1 (RUO)
    浓度
    0.5 mg/ml
    产品详情
    Purified
    Tissue culture supernatant is purified by either protein A/G or affinity purification methods. Both methods yield antibody in solution that is free of most other soluble proteins, lipids, etc. This format provides pure antibody that is suitable for a number of downstream applications including: secondary labeling for flow cytometry or microscopy, ELISA, Western blot, etc.
    应用
    实验应用
    Western blot (Routinely Tested), Bioimaging, Immunohistochemistry (Tested During Development)
    反应种属
    Human (QC Testing), Mouse,Rat,Cow (Tested in Development)
    目标/特异性
    β-Tubulin
    制备和贮存
    存储溶液
    Aqueous buffered solution containing ≤0.09% sodium azide.
    保存方式
    Aqueous buffered solution containing ≤0.09% sodium azide.
    文献
    文献
    研发参考(5) 1. Brown KD, Wood KW, Cleveland DW. The kinesin-like protein CENP-E is kinetochore-associated throughout poleward chromosome segregation during anaphase-A. J Cell Sci. 1996; 109:961-969. (Biology). 2. Cho J-H, Johnson GVW. Primed phosphorylation of tau at Thr231 by glycogen synthase kinase 3β (GSK3β) plays a critical role in regulating tau's ability to bind and stabilize microtubules. J Neurochem. 2004; 88:349-358. (Biology). 3. Helfand BT, Mikami A, Vallee RB, Goldman RD. A requirement for cytoplasmic dynein and dynactin in intermediate filament network assembly and organization. J Cell Biol. 2002; 157(5):795-806. (Biology). 4. Prahlad V, Yoon M, Moir RD, Vale RD, Goldman RD. Rapid movements of vimentin on microtubule tracks: kinesin-dependent assembly of intermediate filament networks. J Cell Biol. 1998; 143(1):159-170. (Biology). 5. Wang Y, Loomis PA, Zinkoswski RP, Binder LI. A novel tau transcript in cultured human neuroblastoma cells expressing nuclear tau. J Cell Biol. 1993; 121(2):257-267. (Biology).

    参考图片

    Immunofluorescent staining of U-87 MG (ATCC HTB-14) cells. Cells were seeded in a 96 well imaging plate (Cat. No. 353219) at ~ 10,000 cells per well.  After overnight incubation, cells were stained using the alcohol perm protocol (see Recommended Assay Procedure) and the anti-Tubulin antibody.  The second step reagent was FITC goat anti mouse Ig (Cat. No. 554001).  The image was taken on a BD Pathway™ 855 bioimaging system using a 20x objective. This antibody also stained A-431 (ATCC CRL-1555), HeLa (ATCC CCL-2), A549 (ATCC CCL-185) and U-2 OS (ATCC HTB-96) cells and can be used with either fix/perm protocol (see Recommended Assay Procedure).

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    货号:
    556321
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    询价
    100ug
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