C21orf59 anticorps (AA 151-250) (Biotin)

N° du produit ABIN1701472

Détail du produit anti-C21orf59 anticorps (Biotin)

Antigène: C21orf59 (Chromosome 21 Open Reading Frame 59 (C21orf59))

Épitope: AA 151-250

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp C21orf59 est conjugé à/à la Biotin

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

Homologie: Human,Mouse,Rat,Cow,Sheep,Pig,Horse

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human C21orf59

Isotype: IgG

Information d'application

Indications d'application: WB 1:300-5000
IHC-P 1:200-400
IHC-F 1:100-500

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 C21orf59

Antigène: C21orf59 (Chromosome 21 Open Reading Frame 59 (C21orf59))

Autre désignation: C21orf59 (C21orf59 Produits)

Synonymes: anticorps C21orf59, anticorps MGC83493, anticorps C3H21orf59, anticorps C21orf48, anticorps RA_m005_jsm24C07r, anticorps chromosome 1 open reading frame, human C21orf59, anticorps chromosome 21 open reading frame 59 L homeolog, anticorps chromosome 3 C21orf59 homolog, anticorps chromosome 21 open reading frame 59, anticorps chromosome 3 open reading frame, human C21orf59, anticorps chromosome 14 open reading frame, human C21orf59, anticorps C1H21ORF59, anticorps c21orf59.L, anticorps C3H21orf59, anticorps c21orf59, anticorps C21orf59, anticorps C14H21orf59

Sujet:

Synonyms: C21orf48, C21orf59, Chromosome 21 open reading frame 59, CU059_HUMAN, FLJ20467, FLJ37137, FLJ40247, Uncharacterized protein C21orf59.

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. C21orf59, also known as C21orf48, is a 290 amino acid protein and its gene product has been provisionally designated C21orf59 pending further characterization.

ID gène: 56683