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Tubulin, alpha 1a (Tuba1a) (N-Term) Peptide

Tuba1a 适用: 人 宿主: 合成 BP, WB
产品编号 ABIN5672912
发货至: 中国
  • 抗原 See all TUBA1A (Tuba1a) products
    TUBA1A (Tuba1a) (Tubulin, alpha 1a (Tuba1a))
    蛋白结构域
    N-Term
    宿主
    资源
    • 3
    合成
    应用范围
    Blocking Peptide (BP), Western Blotting (WB)
    序列
    NACWELYCLE HGIQPDGQMP SDKTIGGGDD SFNTFFSETG AGKHVPRAVF
    产品特性
    This is a synthetic peptide designed for use in combination with anti- TUBA1A Antibody. It may block above mentioned antibody from binding to its target protein in western blot and/or immunohistochecmistry under proper experimental settings. There is no guarantee for its use in other applications.
  • 应用备注
    Optimal working dilution should be determined by the investigator.
    限制
    仅限研究用
  • 状态
    Lyophilized
    溶解方式
    Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.
    储存条件
    -20 °C
    储存方法
    For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
  • 抗原
    TUBA1A (Tuba1a) (Tubulin, alpha 1a (Tuba1a))
    背景
    Microtubules of the eukaryotic cytoskeleton perform essential and diverse functions and are composed of a heterodimer of alpha and beta tubulins. The genes encoding these microtubule constituents belong to the tubulin superfamily, which is composed of six distinct families. Genes from the alpha, beta and gamma tubulin families are found in all eukaryotes. The alpha and beta tubulins represent the major components of microtubules, while gamma tubulin plays a critical role in the nucleation of microtubule assembly. There are multiple alpha and beta tubulin genes, which are highly conserved among species. This gene encodes alpha tubulin and is highly similar to the mouse and rat Tuba1 genes. Northern blotting studies have shown that the gene expression is predominantly found in morphologically differentiated neurologic cells. This gene is one of three alpha-tubulin genes in a cluster on chromosome 12q. Mutations in this gene cause lissencephaly type 3 (LIS3) - a neurological condition characterized by microcephaly, mental retardation, and early-onset epilepsy and caused by defective neuronal migration. Alternative splicing results in multiple transcript variants encoding distinct isoforms.

    Alias Symbols: LIS3, TUBA3, B-ALPHA-1

    Protein Size: 335
    基因ID
    7846
    NCBI登录号
    NM_001270399, NP_001257328
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