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α-tubulin Monoclonal Antibody
Datasheet   

  • Catalog Number:

    E20-53035

  • Amount:

    100ul

  • Molecular Weight:

    50136Da

  • Applications:

    WB;IHC-p;IF/ICC;IP

  • Reactivity:

    Human;Rat;Mouse

  • Purification:

    The antibody was affinity-purified from mouse ascites by affinity-chromatography using specific immunogen.

  • Immunogen:

    Recombinant Protein of Tubulin alpha-1A chain

  • Source:

    Monoclonal, Mouse

  • Western blot analysis of 1) Hela, 2) Rat BrianTissue, 3) Mouse Brain Tissue, diluted at 1:5000.

  • Gene Name:

    TUBA1A

  • Dilution:

    WB: 1:500-10000 IP:1:200 IF 1:200 IHC 1:50-300

  • Background:

    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.

  • Protein Name:

    Tubulin alpha-1A chain

  • Human Gene Id:

    7846/10376

  • Human Swiss Prot No:

    Q71U36/P68363

  • Mouse Gene Id:

    22142/22143

  • Rat Gene Id:

    64158/500929

  • Rat Swiss Prot No:

    P68370/Q6P9V9

  • Specificity:

    The antibody detects endogenousα-tubulin protein.

  • Formulation:

    PBS, pH 7.4, containing 0.5%BSA, 0.02% sodium azide as Preservative and 50% Glycerol.

  • Storage Stability:

    -20°C/1 year

  • Observed Band(KD):

    52

  • Function:

    disease:Defects in TUBA1A are the cause of lissencephaly type 3 (LIS3) [MIM:611603]. LIS is characterized by a smooth brain surface due to the absence (agyria) or reduction (pachygyria) of surface convolutions. It is often associated with psychomotor retardation and seizures. LIS3 features include agyria or pachygyria or laminar heterotopia, severe mental retardation, motor delay, variable presence of seizures, and abnormalities of corpus callosum, hippocampus, cerebellar vermis and brainstem.,function: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.,PTM:Undergoes a tyrosination/detyrosination cycle, the cyclic removal and re-addition of a C-terminal tyrosine residue by the enzymes tubulin tyrosine carboxypeptidase (TTCP) and tubulin tyrosine ligase (TTL), resp

  • Subcellular Location:

    Cytoplasm, cytoskeleton.

  • Expression:

    Expressed at a high level in fetal brain

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Catalog Number

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