KIAA0562 anticorps (AA 451-550) (AbBy Fluor® 680)

N° du produit ABIN4999911

Détail du produit anti-KIAA0562 anticorps (AbBy Fluor® 680)

Antigène: KIAA0562

Épitope: AA 451-550

Reactivité: Humain, Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp KIAA0562 est conjugé à/à la AbBy Fluor® 680

Application: Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))

Réactivité croisée: Humain, Souris

Homologie: Rat,Dog,Cow,Sheep,Horse

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human CEP104/KIAA0562

Isotype: IgG

Information d'application

Indications d'application: IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 μg/μL

Buffer: Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.

Agent conservateur: ProClin

Précaution d'utilisation: This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.

Stock: -20 °C

Stockage commentaire: Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

Date de péremption: 12 months

Détails sur KIAA0562

Antigène: KIAA0562

Autre désignation: CEP104/KIAA0562 (KIAA0562 Produits)

Synonymes: anticorps KIAA0562, anticorps glybp, anticorps kiaa0562, anticorps A930027E11, anticorps AI115523, anticorps Kiaa0562, anticorps mKIAA0562, anticorps GlyBP, anticorps centrosomal protein 104, anticorps centrosomal protein 104kDa, anticorps CEP104, anticorps cep104, anticorps Cep104

Sujet:

Synonyms: CE104_HUMAN, Centrosomal protein of 104 kDa, Cep104, GlyBP, Glycine Binding Protein, glycine-, glutamate- and thienylcyclohexylpiperidine-binding protein, KIAA0562, LOC246295.

Background: Chromosome 1 is the largest human chromosome spanning about 260 million base pairs and making up 8 % of the human genome. There are about 3,000 genes on chromosome 1, and considering the great number of genes there are also a large number of diseases associated with chromosome 1. Notably, the rare aging disease Hutchinson-Gilford progeria is associated with the LMNA gene which encodes lamin A. When defective, the LMNA gene product can build up in the nucleus and cause characteristic nuclear blebs. The mechanism of rapidly enhanced aging is unclear and is a topic of continuing exploration. The MUTYH gene is located on chromosome 1 and is partially responsible for familial adenomatous polyposis. Stickler syndrome, Parkinsons, Gaucher disease and Usher syndrome are also associated with chromosome 1. A breakpoint has been identified in 1q which disrupts the DISC1 gene and is linked to schizophrenia. Aberrations in chromosome 1 are found in a variety of cancers including head and neck cancer, malignant melanoma and multiple myeloma. The KIAA0562 gene product has been provisionally designated KIAA0562 pending further characterization.