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TUBA1B Antikörper (AA 401-451) (Biotin)

TUBA1B Reaktivität: Human, Maus, Ratte WB, ELISA, IHC (p), IHC (fro) Wirt: Kaninchen Polyclonal Biotin
Produktnummer ABIN6982747
  • Target Alle TUBA1B Antikörper anzeigen
    TUBA1B (Tubulin, alpha 1B (TUBA1B))
    Bindungsspezifität
    • 14
    • 6
    • 4
    • 4
    • 3
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 401-451
    Reaktivität
    • 44
    • 24
    • 22
    • 4
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    Human, Maus, Ratte
    Wirt
    • 35
    • 12
    • 1
    Kaninchen
    Klonalität
    • 33
    • 15
    Polyklonal
    Konjugat
    • 26
    • 4
    • 4
    • 3
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Dieser TUBA1B Antikörper ist konjugiert mit Biotin
    Applikation
    • 43
    • 19
    • 17
    • 13
    • 13
    • 10
    • 6
    • 4
    • 4
    • 4
    • 3
    • 2
    • 1
    • 1
    Western Blotting (WB), ELISA, Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunohistochemistry (Frozen Sections) (IHC (fro))
    Kreuzreaktivität
    Human, Maus, Ratte
    Aufreinigung
    Purified by Protein A.
    Immunogen
    KLH conjugated synthetic peptide derived from human TUBA1A + TUBA1B
    Isotyp
    IgG
    Top Product
    Discover our top product TUBA1B Primärantikörper
  • Applikationshinweise
    WB 1:300-5000
    IHC-P 1:200-400
    IHC-F 1:100-500
    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Format
    Liquid
    Konzentration
    1 μg/μL
    Buffer
    Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.
    Konservierungsmittel
    ProClin
    Vorsichtsmaßnahmen
    This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
    Lagerung
    -20 °C
    Informationen zur Lagerung
    Store at -20°C for 12 months.
    Haltbarkeit
    12 months
  • Target
    TUBA1B (Tubulin, alpha 1B (TUBA1B))
    Andere Bezeichnung
    TUBA1A + TUBA1B (TUBA1B Produkte)
    Synonyme
    RGD1565476 antikoerper, K-ALPHA-1 antikoerper, cb944 antikoerper, fb22g06 antikoerper, tuba1 antikoerper, wu:fb22g06 antikoerper, Tuba2 antikoerper, TUBA3 antikoerper, k-alpha-1 antikoerper, tuba antikoerper, Calpha1 antikoerper, Tuba1 antikoerper, TUBA1B antikoerper, tubulin, alpha 1B antikoerper, tubulin alpha 1b antikoerper, tubulin, alpha 1b antikoerper, tubulin alpha 1b L homeolog antikoerper, tubulin alpha-1B chain antikoerper, Tubulin alpha-1B chain antikoerper, Tuba1b antikoerper, TUBA1B antikoerper, tuba1b antikoerper, tuba1b.L antikoerper, LOC100445003 antikoerper, LOC102178700 antikoerper
    Hintergrund

    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]

    Gen-ID
    7846
    UniProt
    Q71U36
    Pathways
    Microtubule Dynamics, M Phase
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