BRWD1-AS2 anticorps (FITC)

N° du produit ABIN1405766

Détail du produit anti-BRWD1-AS2 anticorps (FITC)

Antigène: BRWD1-AS2

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp BRWD1-AS2 est conjugé à/à la FITC

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

Réactivité croisée: Humain

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human C21orf87

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 BRWD1-AS2

Antigène: BRWD1-AS2

Autre désignation: C21orf87 (BRWD1-AS2 Produits)

Synonymes: anticorps BRWD1-IT2, anticorps C21orf87, anticorps NCRNA00257, anticorps BRWD1 antisense RNA 2, anticorps BRWD1-AS2

Sujet:

Synonyms: chromosome 21 open reading frame 87, BRIT2_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 C21orf87 gene product has been provisionally designated C21orf87 pending further characterization.

ID gène: 257357