C7orf34 anticorps (AA 1-80)

N° du produit ABIN1713432

Cet anticorps anti-C7orf34 Polyclonal Lapin (ABIN1713432) détecte spécifiquement C7orf34 dans WB, IF (cc), IF (p), IHC (fro) et IHC (p). L’anticorps est réactif avec des échantillons de Humain.

Aperçu rapide pour C7orf34 anticorps (AA 1-80) (ABIN1713432)

Antigène: C7orf34 (C7ORF34) (Chromosome 7 Open Reading Frame 34 (C7ORF34))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp C7orf34 est non-conjugé

Application: Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunohistochemistry (Frozen Sections) (IHC (fro)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Détail du produit anti-C7orf34 anticorps

Épitope: AA 1-80

Fonction: C7orf34 Polyclonal Antibody

Homologie: Human

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human C7orf34

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: 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: 4 °C,-20 °C

Stockage commentaire: Shipped at 4C. Store at -20C for one year. Avoid repeated freeze/thaw cycles.

Date de péremption: 12 months

Détails sur C7orf34

Antigène: C7orf34 (C7ORF34) (Chromosome 7 Open Reading Frame 34 (C7ORF34))

Autre désignation: C7orf34

Sujet:

Synonyms: C7orf34, CG034_HUMAN, Chromosome 7 open reading frame 34, CTM 1, MSSP-binding protein CTM-1, Uncharacterized protein C7orf34.

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 C7orf34 gene product has been provisionally designated C7orf34 pending further characterization.

ID gène: 135927