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Key Documents

C7488

Sigma-Aldrich

Anti-CENP-E antibody produced in rabbit

IgG fraction of antiserum, buffered aqueous solution

Synonyme(s) :

Anti-Centromere-associated protein-E

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About This Item

Numéro MDL:
Code UNSPSC :
12352203
Nomenclature NACRES :
NA.46

Source biologique

rabbit

Conjugué

unconjugated

Forme d'anticorps

IgG fraction of antiserum

Type de produit anticorps

primary antibodies

Clone

polyclonal

Forme

buffered aqueous solution

Poids mol.

antigen ~310 kDa

Espèces réactives

human

Technique(s)

immunocytochemistry: suitable using human epitheloid carcinoma HeLa cell line.
microarray: suitable
western blot: 1:2,000 using whole extract of HeLa nuclear cell line

Numéro d'accès UniProt

Conditions d'expédition

dry ice

Température de stockage

−20°C

Modification post-traductionnelle de la cible

unmodified

Informations sur le gène

human ... CENPE(1062)

Description générale

Centromere-associated protein-E (CENP-E, 312 kDa) is a member of the kinesin superfamily of microtubule motor proteins and is an integral part of kinetochore corona fibers that link centromere to the spindle microtubules. CENP-E localizes to the kinetochore throughout all phases of mitotic chromosome movement from early prometaphase through anaphase A.

Immunogène

synthetic peptide corresponding to amino acids 2545-2563 located near the C-terminus of human CENP-E conjugated to KLH.

Application

Anti-CENP-E antibody produced in rabbit has been used in:
  • immunoblotting
  • immunofluorescence
  • immunocytochemistry.

Actions biochimiques/physiologiques

Centromere-associated protein-E (CENP-E) plays an important role in attachment of kinetochores to spindle microtubules in the alignment of chromosomes and is an essential component of mitotic checkpoint signaling cascade. It functions as a motor in the initial chromosome movement at the mitotic midzone. CENP-E is associated with minus end-directed microtubule motor activity suggesting that CENP-E might be responsible for poleward kinetochore movements in prometaphase and anaphase A. Suppression of CENP-E synthesis by antisense CENP-E yields chromosomes that are chronically mono-oriented with flattened bipolar spindles and generates spindle poles fragments. Depletion of CENP-E leads to profound checkpoint activation and long-term mitotic arrest. CENP-E has been implicated as a binding partner for the mitotic checkpoint kinase BubR1 during mitosis.

Forme physique

Solution in 0.01 M phosphate buffered saline, pH 7.4, containing 15 mM sodium azide.

Clause de non-responsabilité

Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.

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Code de la classe de stockage

10 - Combustible liquids

Classe de danger pour l'eau (WGK)

nwg

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable


Certificats d'analyse (COA)

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Consulter la Bibliothèque de documents

Determination of the proteomic response to lapatinib treatment using a comprehensive and reproducible ion-current-based proteomics strategy
O Connell K, et al.
Journal of proteomics and genomics research, 1(3), 27-27 (2013)
CENP-E as an essential component of the mitotic checkpoint in vitro
Abrieu A, et al.
Cell, 102(6), 817-826 (2000)
CENP-E forms a link between attachment of spindle microtubules to kinetochores and the mitotic checkpoint
Yao X, et al.
Nature Cell Biology, 2(8), 484-484 (2000)
Crystallization and preliminary crystallographic analysis of the motor domain of human kinetochore-associated protein CENP-E using an automated crystallization procedure
Garcia SI, et al.
Acta Crystallographica Section D, Biological Crystallography, 60(6), 1158-1160 (2004)
CENP-E function at kinetochores is essential for chromosome alignment
Schaar BT, et al.
The Journal of Cell Biology, 139(6), 1373-1382 (1997)

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