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TUBA1B anticorps (AA 401-451) (AbBy Fluor® 647)

TUBA1B Reactivité: Humain, Souris, Rat WB, IF (cc) Hôte: Lapin Polyclonal AbBy Fluor® 647
N° du produit ABIN6980303
  • Antigène Voir toutes TUBA1B Anticorps
    TUBA1B (Tubulin, alpha 1B (TUBA1B))
    Épitope
    • 14
    • 6
    • 4
    • 4
    • 3
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 401-451
    Reactivité
    • 47
    • 30
    • 28
    • 4
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    Humain, Souris, Rat
    Hôte
    • 38
    • 12
    • 1
    Lapin
    Clonalité
    • 39
    • 12
    Polyclonal
    Conjugué
    • 23
    • 4
    • 4
    • 4
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Cet anticorp TUBA1B est conjugé à/à la AbBy Fluor® 647
    Application
    • 40
    • 20
    • 16
    • 12
    • 12
    • 10
    • 7
    • 4
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc))
     Réactivité croisée
    Humain, Souris, Rat
    Purification
    Purified by Protein A.
    Immunogène
    KLH conjugated synthetic peptide derived from human TUBA1A + TUBA1B
    Isotype
    IgG
    Top Product
    Discover our top product TUBA1B Anticorps primaire
  • Indications d'application
    IF(ICC) 1:50-200
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    1 μg/μL
    Buffer
    Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.
    Agent conservateur
    ProClin
    Précaution d'utilisation
    This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
    Stock
    -20 °C
    Stockage commentaire
    Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
    Date de péremption
    12 months
  • Antigène
    TUBA1B (Tubulin, alpha 1B (TUBA1B))
    Autre désignation
    TUBA1A + TUBA1B (TUBA1B Produits)
    Synonymes
    anticorps RGD1565476, anticorps K-ALPHA-1, anticorps cb944, anticorps fb22g06, anticorps tuba1, anticorps wu:fb22g06, anticorps Tuba2, anticorps TUBA3, anticorps k-alpha-1, anticorps tuba, anticorps Calpha1, anticorps Tuba1, anticorps TUBA1B, anticorps tubulin, alpha 1B, anticorps tubulin alpha 1b, anticorps tubulin, alpha 1b, anticorps tubulin alpha 1b L homeolog, anticorps tubulin alpha-1B chain, anticorps Tubulin alpha-1B chain, anticorps Tuba1b, anticorps TUBA1B, anticorps tuba1b, anticorps tuba1b.L, anticorps LOC100445003, anticorps LOC102178700
    Sujet

    Synonyms: TUBA1A + TUBA1B, Tubulin, Alpha 1b, Tubulin Alpha-Ubiquitous Chain, Alpha-Tubulin Ubiquitous, Tubulin K-Alpha-1, Tubulin, Alpha, Ubiquitous, Tubulin Alpha-1B Chain, Alpha Tubulin, Ubiquitous, K-ALPHA-1, Tubulin Alpha, TBA1B_HUMAN, Tubulin, Alpha 1a, TUBA3, Tubulin Alpha-3 Chain, Tubulin B-Alpha-1, LIS3, Tubulin, Alpha, Brain-Specific, Tubulin Alpha-1A Chain, Alpha-Tubulin 3, Brain-Specific, Hum-A-Tub1, Hum-A-Tub2, B-ALPHA-1, TBA1A_HUMAN, ,____alpha

    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. 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. [provided by RefSeq, Jul 2012]

    ID gène
    7846
    UniProt
    Q71U36
    Pathways
    Dynamique des Microtubules, M Phase
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