C4orf22 anticorps (Cy3)

N° du produit ABIN1423685

L’anticorps Lapin Polyclonal anti-C4orf22 a été validé pour WB et IF (p). Il convient pour détecter C4orf22 dans des échantillons de Humain, Souris et Rat.

Aperçu rapide pour C4orf22 anticorps (Cy3) (ABIN1423685)

Antigène: C4orf22 (Chromosome 4 Open Reading Frame 22 (C4orf22))

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp C4orf22 est conjugé à/à la Cy3

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

Détail du produit anti-C4orf22 anticorps (Cy3)

Réactivité croisée: Humain, Souris, Rat

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human C4orf22

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: 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 C4orf22

Antigène: C4orf22 (Chromosome 4 Open Reading Frame 22 (C4orf22))

Autre désignation: C4orf22

Sujet:

Synonyms: Chromosome 4 open reading frame 22, Hypothetical protein LOC255119, MGC35043, Uncharacterized protein C4orf22, CD022_HUMAN.

Background: C4orf22 is a 233 amino acid protein that exists as three alternatively spliced isoforms and are encoded by a gene encoding maping to human chromosome 4, which represents approximately 6 % of the human genome and contains nearly 900 genes. Notably, the Huntingtin gene, which is found to encode an expanded glutamine tract in cases of Huntington's disease, is on chromosome 4. FGFR-3 is also encoded by a gene that maps to chromosome 4 and has been associated with thanatophoric dwarfism, achondroplasia, Muenke syndrome and bladder cancer. Chromosome 4 is also tied to Ellis-van Creveld syndrome, methylmalonic acidemia and polycystic kidney disease.

ID gène: 255119