C21orf58 anticorps (Cy7)

N° du produit ABIN1423610

L’anticorps Lapin Polyclonal anti-C21orf58 a été validé pour WB et IF (p). Il convient pour détecter C21orf58 dans des échantillons de Humain, Souris et Rat.

Aperçu rapide pour C21orf58 anticorps (Cy7) (ABIN1423610)

Antigène: C21orf58 (Chromosome 21 Open Reading Frame 58 (C21orf58))

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp C21orf58 est conjugé à/à la Cy7

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

Détail du produit anti-C21orf58 anticorps (Cy7)

Réactivité croisée: Humain, Souris, Rat

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human C21orf58

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 C21orf58

Antigène: C21orf58 (Chromosome 21 Open Reading Frame 58 (C21orf58))

Autre désignation: C21orf58

Sujet:

Synonyms: C21orf58, Chromosome 21 open reading frame 58, CU058_HUMAN, Hypothetical protein LOC54058, Uncharacterized protein C21orf58.

Background: The smallest of the human chromosomes, 21 makes up about 1.5 % of the human genome. Chromosome 21 contains nearly 300 genes and 47 million base pairs. Down syndrome, also known as trisomy 21, is the disease most commonly associated with chromosome 21. Alzheimer's disease, Jervell and Lange-Nielsen syndrome and amyotrophic lateral sclerosis are also associated with chromosome 21. Translocations are found to occur between chromosome 21 and 8, and chromosome 21 and 12, in certain leukemias. The C21orf58 gene product has been provisionally designated C21orf58 pending further characterization.

ID gène: 54058