C7orf44 anticorps (AA 51-146) (Biotin)

N° du produit ABIN1699933

Cet anticorps Lapin Polyclonal détecte spécifiquement C7orf44 dans WB, IHC (fro) et IHC (p). Il présente une réactivité avec des échantillons de Humain.

Aperçu rapide pour C7orf44 anticorps (AA 51-146) (Biotin) (ABIN1699933)

Antigène: C7orf44 (Chromosome 7 Open Reading Frame 44 (C7orf44))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp C7orf44 est conjugé à/à la Biotin

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

Détail du produit anti-C7orf44 anticorps (Biotin)

Épitope: AA 51-146

Fonction: C7orf44 Polyclonal Antibody, Biotin Conjugated

Homologie: Human

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human C7orf44

Isotype: IgG

Information d'application

Indications d'application: WB(1:300-5000),

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, 0.02 % 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 C7orf44

Antigène: C7orf44 (Chromosome 7 Open Reading Frame 44 (C7orf44))

Autre désignation: C7orf44

Sujet:

Synonyms: Chromosome 7 open reading frame 44, FLJ10803, Hypothetical protein LOC55744, Uncharacterized protein C7orf44,COA1_HUMAN.

Background: Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterized by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia. The C7orf44 gene product has been provisionally designated C7orf44 pending further characterization.

ID gène: 55744