C7orf43 anticorps (AA 301-400)

N° du produit ABIN1713434

L’anticorps anti-C7orf43 Polyclonal Lapin est utilisé pour la détection de C7orf43 dans des échantillons de Humain. Il a été validé pour IF (cc), IF (p), ELISA, IHC (fro), IHC (p) et ICC.

Aperçu rapide pour C7orf43 anticorps (AA 301-400) (ABIN1713434)

Antigène: C7orf43 (Chromosome 7 Open Reading Frame 43 (C7orf43))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp C7orf43 est non-conjugé

Application: Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), ELISA, Immunohistochemistry (Frozen Sections) (IHC (fro)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunocytochemistry (ICC)

Détail du produit anti-C7orf43 anticorps

Épitope: AA 301-400

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

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human C7ORF43

Isotype: IgG

Information d'application

Indications d'application: ELISA 1:500-1000
IHC-P 1:200-400
IHC-F 1:100-500
IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200
ICC 1:100-500

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 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.

Date de péremption: 12 months

Détails sur C7orf43

Antigène: C7orf43 (Chromosome 7 Open Reading Frame 43 (C7orf43))

Autre désignation: C7ORF43

Sujet:

Synonyms: C7orf43, CG043_HUMAN, Chromosome 7 open reading frame 43, DKFZp761G0712, FLJ10925, Hypothetical protein LOC55262, Uncharacterized protein C7orf43.

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 C7orf43 gene product has been provisionally designated C7orf43 pending further characterization.

ID gène: 55262