CTTNBP2NL anticorps (AA 5-110) (AbBy Fluor® 488)

N° du produit ABIN6942710

Cet anticorps anti-CTTNBP2NL est un anticorps Lapin Polyclonal détectant CTTNBP2NL dans WB, IF (cc) et IF (p). Adapté pour Rat.

Aperçu rapide pour CTTNBP2NL anticorps (AA 5-110) (AbBy Fluor® 488) (ABIN6942710)

Antigène: CTTNBP2NL (CTTNBP2 N-terminal Like (CTTNBP2NL))

Reactivité: Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp CTTNBP2NL est conjugé à/à la AbBy Fluor® 488

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

Détail du produit anti-CTTNBP2NL anticorps (AbBy Fluor® 488)

Épitope: AA 5-110

Réactivité croisée: Rat

Homologie: Human,Mouse,Cow,Pig,Horse,Chicken,Rabbit

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human CTTNBP2NL

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 CTTNBP2NL

Antigène: CTTNBP2NL (CTTNBP2 N-terminal Like (CTTNBP2NL))

Autre désignation: CTTNBP2NL

Sujet:

Synonyms: CT2NL_HUMAN, CTTNBP2 N terminal like, CTTNBP2 N terminal like protein, CTTNBP2 N-terminal-like protein, Cttnbp2nl, DKFZp547A023, FLJ13278, KIAA1433.

Background: CTTNBP2NL is a 639 amino acid protein that is encoded by a gene that maps to human chromosome 1p13.2. 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.

ID gène: 55917

UniProt: Q9P2B4