C21orf62 anticorps (Biotin)

N° du produit ABIN1405723

Détail du produit anti-C21orf62 anticorps (Biotin)

Antigène: C21orf62 (Chromosome 21 Open Reading Frame 62 (C21orf62))

Reactivité: Humain, Rat, Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp C21orf62 est conjugé à/à la Biotin

Application: Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Réactivité croisée: Humain, Souris, Rat

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human C21ORF62

Isotype: IgG

Information d'application

Indications d'application: WB 1:300-5000
IHC-P 1:200-400

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 for 12 months.

Date de péremption: 12 months

Détails sur C21orf62

Antigène: C21orf62 (Chromosome 21 Open Reading Frame 62 (C21orf62))

Autre désignation: C21ORF62 (C21orf62 Produits)

Synonymes: anticorps B37, anticorps PRED81, anticorps C21orf120, anticorps MGC88933, anticorps chromosome 21 open reading frame 62, anticorps chromosome 1 open reading frame, human C21orf62, anticorps chromosome 3 open reading frame, human C21orf62, anticorps C21orf62, anticorps C1H21ORF62, anticorps c21orf62, anticorps C3H21orf62

Sujet:

Synonyms: B37, C21orf120, Chromosome 21 open reading frame 62, Hypothetical protein LOC56245, PRED81, Uncharacterized protein C21orf62, CU062_HUMAN.

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 C21orf62 gene product has been provisionally designated C21orf62 pending further characterization.

ID gène: 56245