| Overview |
| bs-20496R-Cy7 |
| TUBA1A + TUBA1B Polyclonal Antibody, Cy7 Conjugated |
| WB, IF(ICC) |
| Human, Mouse, Rat |
| Specifications |
| Cy7 |
| Rabbit |
| KLH conjugated synthetic peptide derived from human TUBA1A + TUBA1B |
| 401-451/451 |
| Polyclonal |
| IgG |
| 1ug/ul |
| Purified by Protein A. |
| Aqueous buffered solution containing 0.01M TBS (pH 7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol. |
| Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles. |
| Target |
| 7846 |
| Q71U36 |
| 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 |
| 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] |
| Application Dilution |
| WB |
1:300-5000 |
| IF(ICC) |
1:50-200 |
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