CCDC19 anticorps (AbBy Fluor® 350)

N° du produit ABIN908013

Cet anticorps anti-CCDC19 est un anticorps Lapin Polyclonal détectant CCDC19 dans WB. Adapté pour Humain, Rat et Souris.

Aperçu rapide pour CCDC19 anticorps (AbBy Fluor® 350) (ABIN908013)

Antigène: CCDC19 (Coiled-Coil Domain Containing 19 (CCDC19))

Reactivité: Humain, Rat, Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp CCDC19 est conjugé à/à la AbBy Fluor® 350

Application: Western Blotting (WB)

Détail du produit anti-CCDC19 anticorps (AbBy Fluor® 350)

Homologie: Human,Mouse,Rat,Cow,Sheep,Horse,Rabbit

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human CCDC19

Isotype: IgG

Information d'application

Indications d'application: IF(IHC-P) 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: Sodium azide

Précaution d'utilisation: This product contains Sodium azide: 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 CCDC19

Antigène: CCDC19 (Coiled-Coil Domain Containing 19 (CCDC19))

Autre désignation: Ccdc19

Sujet:

Synonyms: Coiled coil domain containing 19, Nasopharyngeal epithelium specic protein 1, NESG1, RP11 190A12.6, CCD19_HUMAN.

Background: CCDC19 is a 466 amino acid protein encoded by a gene mapping to human chromosome 1. 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, Parkinson?s, 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.

ID gène: 25790