BubR1 rabbit pAb

BubR1 rabbit pAb

AO-06-ES1801-50

BubR1 rabbit pAb 50μL

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Antibody Product Overview

ELK.NoES1801
Product nameBubR1 rabbit pAb
ReactivityHuman;Mouse
ApplicationsWB;ELISA
Other nameBUB1B; BUBR1; MAD3L; SSK1; Mitotic checkpoint serine/threonine-protein kinase BUB1 beta; MAD3/BUB1-related protein kinase; hBUBR1; Mitotic checkpoint kinase MAD3L; Protein SSK1
Size50μL
Unit price ($)148
Human gene ID701
Human Swiss-ProtO60566
SourceRabbit
IsotypeIgG
TargetBubR1
Fields>>Cell cycle;>>Human T-cell leukemia virus 1 infection
Gene nameBUB1B
Protein nameMitotic checkpoint serine/threonine-protein kinase BUB1 beta
Human gene linkView Human Gene
Human Swiss linkView Human Swiss-Prot
Mouse gene ID12236
Mouse gene linkView Mouse Gene
Mouse Swiss-ProtQ9Z1S0
Mouse Swiss linkView Mouse Swiss-Prot
Rat gene ID
Rat gene link
Rat Swiss-Prot
Rat Swiss link
ImmunogenThe antiserum was produced against synthesized peptide derived from human BUB1B. AA range:341-390
SpecificityBubR1 Polyclonal Antibody detects endogenous levels of BubR1 protein.
FormulationLiquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
ClonalityPolyclonal
DilutionWestern Blot: 1/500 - 1/2000. ELISA: 1/20000. Not yet tested in other applications.
PurificationThe antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Concentration1 mg/ml
Storage stability-20°C/1 year
Molecular Weight (Da)
Observed band (KD)130kD
BackgroundThis gene encodes a kinase involved in spindle checkpoint function. The protein has been localized to the kinetochore and plays a role in the inhibition of the anaphase-promoting complex/cyclosome (APC/C), delaying the onset of anaphase and ensuring proper chromosome segregation. Impaired spindle checkpoint function has been found in many forms of cancer. [provided by RefSeq, Jul 2008],
Functioncatalytic activity:ATP + a protein = ADP + a phosphoprotein.,disease:Defects in BUB1B are associated with tumor formation.,disease:Defects in BUB1B are the cause of mosaic variegated aneuploidy syndrome (MVA) [MIM:257300]. MVA is a severe autosomal recessive developmental disorder characterized by mosaic aneuploidies, predominantly trisomies and monosomies, involving multiple different chromosomes and tissues. The proportion of aneuploid cells varies but is usually more than 25% and is substantially greater than in normal individuals. Affected individuals typically present with severe intrauterine growth retardation and microcephaly. Eye anomalies, mild dysmorphism, variable developmental delay, and a broad spectrum of additional congenital abnormalities and medical conditions may also occur. The risk of malignancy is high, with rhabdomyosarcoma, Wilms tumor and leukemia reported in seve
Subcellular locationCytoplasm. Nucleus. Chromosome, centromere, kinetochore. Cytoplasm, cytoskeleton, microtubule organizing center, centrosome. Cytoplasmic in interphase cells. Associates with the kinetochores in early prophase. Kinetochore localization requires BUB1, PLK1 and KNL1.
ExpressionHighly expressed in thymus followed by spleen. Preferentially expressed in tissues with a high mitotic index.

Additional Images

Image 1
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Western Blot analysis of various cells using BubR1 Polyclonal Antibody
Image 2
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Western blot analysis of lysates from HeLa and HepG2 cells, treated with H2O2 100uM 30', using BUB1B Antibody. The lane on the right is blocked with the synthesized peptide.
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: AO-06-ES1801-50
: 10 Produits
Hurry! only 10 items left in stock.

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