C7ORF57 anticorps (AA 161-260)

N° du produit ABIN1714347

Cet anticorps anti-C7ORF57 Polyclonal Lapin (ABIN1714347) détecte spécifiquement C7ORF57 dans IF (cc), IF (p), IHC (fro) et IHC (p). L’anticorps est réactif avec des échantillons de Humain.

Aperçu rapide pour C7ORF57 anticorps (AA 161-260) (ABIN1714347)

Antigène: C7ORF57 (Chromosome 7 Open Reading Frame 57 (C7ORF57))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp C7ORF57 est non-conjugé

Application: 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-C7ORF57 anticorps

Épitope: AA 161-260

Fonction: C7orf57 Polyclonal Antibody

Réactivité croisée: Rat

Homologie: Human,Mouse,Cow,Sheep,Horse

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human C7orf57

Isotype: IgG

Information d'application

Indications d'application: Optimal working dilution should be determined by the investigator.

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 C7ORF57

Antigène: C7ORF57 (Chromosome 7 Open Reading Frame 57 (C7ORF57))

Autre désignation: C7orf57

Sujet:

Synonyms: C7orf57, CG057_HUMAN, Chromosome 7 open reading frame 57, Uncharacterized protein C7orf57.

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 C7orf57 gene product has been provisionally designated C7orf57 pending further characterization.

ID gène: 136288

UniProt: Q8NEG2