TUBA1A/TUBA1B Antibody (PACO00086)
- SKU:
- PACO00086
- Product Type:
- Antibody
- Reactivity:
- Human
- Mouse
- Rat
- Host Species:
- Rabbit
- Isotype:
- IgG
- Applications:
- WB
- Antibody Type:
- Polyclonal Antibody
- Conjugation:
- Unconjugated
Description
TUBA1A/TUBA1B Antibody (PACO00086)
The TUBA1A/TUBA1B Polyclonal Antibody (PACO00086) is a valuable tool for researchers studying tubulin alpha-1A and tubulin alpha-1B proteins. Tubulins are essential components of microtubules, playing a crucial role in cell division, intracellular transport, and cell shape maintenance. This antibody, produced in rabbits, is highly specific to human samples and is validated for use in Western blot applications.By binding to TUBA1A and TUBA1B proteins, this antibody enables accurate detection and analysis in a variety of cell types, making it ideal for investigations in cell biology, neuroscience, and cancer research.
The functions of tubulin alpha-1A and alpha-1B are vital for cellular processes, and abnormalities in their expression have been linked to diseases such as cancer, neurodevelopmental disorders, and neurodegenerative diseases.Understanding the roles of TUBA1A and TUBA1B in cellular functions and diseases is crucial for developing targeted therapies and interventions. The TUBA1A/TUBA1B Polyclonal Antibody provides researchers with a reliable tool to advance knowledge in these areas and potentially contribute to the development of novel treatments.
Antibody Name: | TUBA1A/TUBA1B Antibody |
Antibody SKU: | PACO00086 |
Size: | 50ug |
Host Species: | Rabbit |
Tested Applications: | WB |
Recommended Dilutions: | |
Species Reactivity: | Human, Mouse, Rat |
Immunogen: | Recombinant Protein |
Form: | Liquid |
Storage Buffer: | PBS, pH 7.4, containing 0.02% sodium azide as Preservative and 50% Glycerol. |
Purification Method: | Affinity purification |
Clonality: | Polyclonal |
Isotype: | IgG |
Conjugate: | Non-conjugated |
Synonyms: | Tubulin alpha-1A chain |
UniProt Protein Function: | TUBA1A: 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. Dimer of alpha and beta chains. Expressed at a high level in fetal brain. Belongs to the tubulin family. |
UniProt Protein Details: | Protein type:Motility/polarity/chemotaxis; Cytoskeletal Chromosomal Location of Human Ortholog: 12q13.12 Cellular Component: microtubule; recycling endosome; cytoplasmic microtubule; cytosol; nucleus Molecular Function:GTPase activity; protein domain specific binding; protein binding; GTP binding; structural constituent of cytoskeleton; structural molecule activity Biological Process: protein polymerization; 'de novo' posttranslational protein folding; cellular protein metabolic process; protein folding; cell division; organelle organization and biogenesis; cytoskeleton-dependent intracellular transport; mitotic cell cycle; G2/M transition of mitotic cell cycle; microtubule-based process Disease: Lissencephaly 3 |
NCBI Summary: | 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. [provided by RefSeq, Jul 2017] |
UniProt Code: | Q71U36 |
NCBI GenInfo Identifier: | 55977864 |
NCBI Gene ID: | 7846 |
NCBI Accession: | Q71U36.1 |
UniProt Secondary Accession: | Q71U36,P68363, |
UniProt Related Accession: | Q71U36 |
Molecular Weight: | ~ 55kDa |
NCBI Full Name: | Tubulin alpha-1A chain |
NCBI Synonym Full Names: | tubulin alpha 1a |
NCBI Official Symbol: | TUBA1AÂ Â |
NCBI Official Synonym Symbols: | LIS3; TUBA3; B-ALPHA-1Â Â |
NCBI Protein Information: | tubulin alpha-1A chain |
UniProt Protein Name: | Tubulin alpha-1A chain |
UniProt Synonym Protein Names: | Alpha-tubulin 3; Tubulin B-alpha-1; Tubulin alpha-3 chain |
Protein Family: | Tubulin |
UniProt Gene Name: | TUBA1AÂ Â |
UniProt Entry Name: | TBA1A_HUMAN |