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TUBA1A

Anti-TUBA1A Products
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- Species Reactivity: Bovine, Human, Mouse
- Type: Human IgG
- Application: ICC
- Human Anti-TUBA1A Recombinant Antibody (clone F2C) (DrMAB-1073)
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- Species Reactivity: Mouse, Bovine, Human
- Type: Human IgG
- Application: ELISA
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- Species Reactivity: Mouse
- Type: Mouse antibody
- Application: ICC, IF
- Rabbit Anti-TUBA1A Polyclonal Antibody (MRO-0203YJ)
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- Species Reactivity: Human, Mouse, Rat, Pig, Bovine, Rabbit, Chicken, Plants, Fish
- Type: Rabbit IgG
- Application: WB, IHC, IF, ICC, ELISA
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- Species Reactivity: Zebrafish
- Type: Mouse IgG
- Application: WB
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- Species Reactivity: Human, Rat, Mouse
- Type: Mouse IgG
- Application: WB, IHC-P, IF, IP
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- Species Reactivity: Human, Rat, Mouse
- Type: Mouse IgG
- Application: WB, IHC-P, IF, IP
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- Species Reactivity: Human, Rat, Mouse
- Type: Mouse IgG
- Application: WB, IHC-P, IF, IP
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- Species Reactivity: Human, Rat, Mouse
- Type: Mouse IgG
- Application: WB, IHC-P, IF, IP
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- Species Reactivity: Human, Rat, Mouse
- Type: Mouse IgG
- Application: WB, IHC-P, IF, IP
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- Species Reactivity: Human, Rat, Mouse
- Type: Mouse IgG
- Application: WB, IHC-P, IF, IP
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- Species Reactivity: Human, Rat, Mouse
- Type: Mouse IgG
- Application: WB, IHC-P, IF, IP
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- Species Reactivity: Human, Rat, Mouse
- Type: Mouse IgG
- Application: WB, IHC-P, IF, IP
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- Species Reactivity: Human, Rat, Mouse
- Type: Mouse IgG
- Application: WB, IHC-P, IF, IP
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- Species Reactivity: Human, Rat, Mouse
- Type: Mouse IgG
- Application: WB, IHC-P, IF, IP
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- Species Reactivity: Human, Rat, Mouse
- Type: Mouse IgG
- Application: WB, IHC-P, IF, IP
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- Species Reactivity: Human, Rat, Mouse
- Type: Mouse IgG
- Application: WB, IHC-P, IF, IP
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- Species Reactivity: Human, Rat, Mouse
- Type: Mouse IgG
- Application: WB, IHC-P, IF, IP
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- Species Reactivity: Human, Rabbit, Rat, Mouse
- Type: Mouse IgG2a
- Application: ELISA, WB, IHC, IF, FC, IP
- Mouse Anti-TUBA1A Recombinant Antibody (VS3-WK1044) (VS3-WK1044)
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- Derivation: Mouse
- Species Reactivity: Human, Mouse, Rat
- Type: Mouse IgG
- Application: WB, IHC, IF, ICC, IP
- AbPlus™ Anti-TUBA1A Magnetic Beads (8F11) (VS-0424-XY266)
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- Target: TUBA1A
- Target Species: Human, Rat, Mouse
- Application: IP, Protein Purification
- Anti-TUBA1A Immunohistochemistry Kit (VS-0325-XY2391)
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- Species Reactivity: Human, Mouse, Rat
- Target: TUBA1A
- Application: IHC
- Anti-Mouse TUBA1A Immunohistochemistry Kit (VS-0525-XY7600)
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- Species Reactivity: Human, Mouse, Rat
- Target: TUBA1A
- Application: IHC
- Anti-Human TUBA1A Immunohistochemistry Kit (VS-0525-XY7599)
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- Species Reactivity: Human
- Target: TUBA1A
- Application: IHC
- Anti-Rat TUBA1A Immunohistochemistry Kit (VS-0525-XY7601)
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- Species Reactivity: Human, Mouse, Rat
- Target: TUBA1A
- Application: IHC
- Anti-Monkey TUBA1A Immunohistochemistry Kit (VS-0525-XY7602)
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- Species Reactivity: Human, Mouse, Rat, Monkey, Monkey, Yeast
- Target: TUBA1A
- Application: IHC
- Anti-Fruit fly TUBA1A Immunohistochemistry Kit (VS-0525-XY7603)
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- Species Reactivity: Human, Mouse, Rat, Fruit fly, Yeast
- Target: TUBA1A
- Application: IHC
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For Research Use Only. Not For Clinical Use.
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 blot 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, intellectual disability, and early-onset epilepsy caused by defective neuronal migration. Alternative splicing results in multiple transcript variants encoding distinct isoforms.