β Tubulin rabbit pAb

β Tubulin rabbit pAb

AO-06-ES20589-50

β Tubulin rabbit pAb 50μL

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€299.00
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Antibody Product Overview

ELK.NoES20589
Product nameβ Tubulin rabbit pAb
ReactivityHuman;Mouse;Rat
ApplicationsWB
Other nameTUBB3; TUBB4; Tubulin beta-3 chain; Tubulin beta-4 chain; Tubulin beta-III
Size50μL
Unit price ($)148
Human gene ID10381
Human Swiss-ProtQ13509
SourceRabbit
IsotypeIgG
TargetTubulin β
Fields>>Phagosome;>>Gap junction;>>Alzheimer disease;>>Parkinson disease;>>Amyotrophic lateral sclerosis;>>Huntington disease;>>Prion disease;>>Pathways of neurodegeneration - multiple diseases;>>Pathogenic Escherichia coli infection;>>Salmonella infection
Gene nameTUBB3
Protein nameTubulin beta-3 chain
Human gene linkView Human Gene
Human Swiss linkView Human Swiss-Prot
Mouse gene ID22152
Mouse gene linkView Mouse Gene
Mouse Swiss-ProtQ9ERD7
Mouse Swiss linkView Mouse Swiss-Prot
Rat gene ID246118
Rat gene linkView Rat Gene
Rat Swiss-ProtQ4QRB4
Rat Swiss linkView Rat Swiss-Prot
ImmunogenRecombinant Protein of Tubulin beta
SpecificityThe antibody detects endogenous β tubulin protein.
FormulationPBS, pH 7.4, containing 0.5%BSA, 0.02% sodium azide as Preservative and 50% Glycerol.
ClonalityPolyclonal
DilutionWB: 1:2000-5000
PurificationThe antibody was affinity-purified from rabbit antiserum by affinity-chromatography using specific immunogen.
Concentration
Storage stability-20°C/1 year
Molecular Weight (Da)
Observed band (KD)55kD
Backgroundtubulin beta 3 class III(TUBB3) Homo sapiens This gene encodes a class III member of the beta tubulin protein family. Beta tubulins are one of two core protein families (alpha and beta tubulins) that heterodimerize and assemble to form microtubules. This protein is primarily expressed in neurons and may be involved in neurogenesis and axon guidance and maintenance. Mutations in this gene are the cause of congenital fibrosis of the extraocular muscles type 3. Alternate splicing results in multiple transcript variants. A pseudogene of this gene is found on chromosome 6. [provided by RefSeq, Oct 2010],
Functiondomain:The highly acidic C-terminal region may bind cations such as calcium.,function:Receptor for MSH (alpha, beta and gamma) and ACTH. The activity of this receptor is mediated by G proteins which activate adenylate cyclase.,function: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.,polymorphism:Genetic variations in MC1R are associated with variation in skin/hair/eye pigmentation type 2 (SHEP2) [MIM:266300]. Hair, eye and skin pigmentation are among the most visible examples of human phenotypic variation, with a broad normal range that is subject to substantial geographic stratification. In the case of skin, individuals tend to have lighter pigmentation with increasing distance from the equator. By contrast, the majority of variation in human eye and hair col
Subcellular locationCytoplasm, cytoskeleton . Cell projection, growth cone . Cell projection, lamellipodium . Cell projection, filopodium .
ExpressionExpression is primarily restricted to central and peripheral nervous system. Greatly increased expression in most cancerous tissues.

Additional Images

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Western blot analysis of 1) Hela, 2) Mouse Brain, 3) Rat Brain tissue, diluted at 1:5000. Secondary antibody(catalog#:RS0002) was diluted at 1:20000
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: AO-06-ES20589-50
: 10 Items
Hurry! only 10 items left in stock.

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