TUBB1 Monoclonal Antibody
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中文名称:TUBB1鼠单克隆抗体
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货号:CSB-MA000192
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规格:¥1090
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图片:
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其他:
产品详情
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产品描述:CUSABIO货号:CSB-MA000192 TUBB1单克隆抗体是针对β-微管蛋白家族成员TUBB1研发的特异性检测工具,该靶点在血小板形成过程中发挥关键作用,参与调控巨核细胞分化和血小板释放机制,其表达异常与血小板减少症等血液系统疾病密切相关。本产品采用杂交瘤技术制备,具有高亲和力与优异特异性,可精准识别人类、小鼠及大鼠样本中TUBB1蛋白,适用于ELISA检测和Western Blot免疫印迹实验,满足不同实验体系需求。经严格验证的抗体性能可有效支持血小板生成机制研究、巨核细胞分化过程分析以及血小板相关疾病的分子机制探索,为血液系统疾病研究、心血管病理模型构建及药物作用靶点筛选等科研领域提供可靠工具。该TUBB1抗体特别适用于体外培养细胞模型、组织裂解液等样本的蛋白水平检测,兼容常规SDS-PAGE及转膜实验条件,是研究细胞骨架动态调控与血小板功能关联性的理想选择。
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Uniprot No.:
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基因名:
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别名:2810484G07Rik antibody; beta 1 tubulin antibody; Beta tubulin 1, class VI antibody; Beta-tubulin antibody; Class VI beta tubulin antibody; dJ543J19.4 antibody; M(beta)1 antibody; TBB1_HUMAN antibody; TUBB1 antibody; Tubulin beta 1 class VI antibody; Tubulin beta-1 chain antibody; Tubulin, beta 1 antibody; tubulin, beta1 antibody
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宿主:Mouse
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反应种属:Human,Mouse,Rat
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免疫原:Synthetic Peptide
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免疫原种属:H, R, M
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标记方式:Non-conjugated
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抗体亚型:IgG
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克隆号:29E1
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浓度:It differs from different batches. Please contact us to confirm it.
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保存缓冲液:PBS, pH 7.4, containing 0.02% sodium azide as Preservative and 50% Glycerol.
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产品提供形式:Liquid
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应用范围:ELISA,WB
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推荐稀释比:
Application Recommended Dilution WB 1:500-1:5000 -
Protocols:
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储存条件:Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
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货期:Basically, we can dispatch the products out in 1-3 working days after receiving your orders. Delivery time maybe differs from different purchasing way or location, please kindly consult your local distributors for specific delivery time.
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用途:For Research Use Only. Not for use in diagnostic or therapeutic procedures.
相关产品
靶点详情
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功能:Tubulin is the major constituent of microtubules. It binds two moles of GTP, one at an exchangeable site on the beta chain and one at a non-exchangeable site on the alpha chain.
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基因功能参考文献:
- Neonatal platelets exhibit low levels of the Stx11-Munc18b complex (essential component of the SNARE machinery) and of beta1-tubulin. These developmental deficiencies are associated with defects in platelet adhesion, spreading and secretion. PMID: 29044293
- novel DCX mutation (p.D90G, NP_000546.2) appeared to be a major causative variant, whereas the novel mutation of TUBB1 (p.R62fsX, NP_110400.1) was found only in patients with more-severe intellectual disability in Familial pachygyria PMID: 26743950
- Analysis of the TUBB1 gene revealed three known missense variants in heterozygous state which in combination might explain the beta1-tubulin defect. PMID: 26540125
- TUBB1 R307H SNP is significantly associated with the degree of thrombocytopenia in congenital and acquired platelet disorders, and may affect platelets by altering microtubule behavior. PMID: 25529050
- Data indicate that ABCB1 protein, beta tubulin I and III (betaI, and betaIII tubulin) might contribute to the multidrug resistance (MDR) of MCF7/DOC and be potential therapeutic targets for overcoming MDR of breast cancer. PMID: 24894670
- TUBB1 mutation disrupting microtubule assembly impairs proplatelet formation and results in congenital macrothrombocytopenia. PMID: 24344610
- our findings define beta-tubulin VI as a hematologic isotype with significant genetic variation in humans that may affect the myelosuppresive action of microtubule-binding drugs PMID: 22805305
- homozygous status of P43 genetic polymorphism causes alterations in platelet ultrastructure PMID: 21384078
- Studies show that BFBTS bound and modified beta-tubulin at residue Cys12, forming beta-tubulin-SS-fluorobenzyl. PMID: 19996274
- SLPI localizes in part along the megakaaryocyte and platelet cytoskeleton by virtue of specific interactions with beta1 tubulin. PMID: 15315966
- the platelet Q43P beta1-tubulin substitution is frequent in the healthy population and may protect men against arterial thrombosis PMID: 15956286
- The TUBB1 Q43P polymorphism, by causing a lower reactivity in platelets carrying the variant form of b1-tubulin, protects against thrombotic disorders but increases the risk of intracerebral hemorrhage in men. PMID: 17488662
- biophysical analysis of carboxy-terminal tail conformation of human beta-tubulin isotypes PMID: 17993481
- Mutation of the beta1-tubulin gene associated with congenital macrothrombocytopenia affecting microtubule assembly. PMID: 18849486
- TUBB1 Q43P polymorphism does not protect against acute coronary syndrome and premature myocardial infarction. PMID: 19132255
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相关疾病:Macrothrombocytopenia, autosomal dominant, TUBB1-related (MAD-TUBB1)
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亚细胞定位:Cytoplasm, cytoskeleton.
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蛋白家族:Tubulin family
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组织特异性:Hematopoietic cell-specific. Major isotype in leukocytes, where it represents 50% of all beta-tubulins.
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数据库链接:
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