C7orf29 anticorps (AA 131-236)

N° du produit ABIN1713431

L’anticorps Lapin Polyclonal anti-C7orf29 a été validé pour ELISA, WB, IF (cc), IF (p), IHC (fro), IHC (p) et ICC. Il convient pour détecter C7orf29 dans des échantillons de Humain.

Aperçu rapide pour C7orf29 anticorps (AA 131-236) (ABIN1713431)

Antigène: C7orf29 (C7ORF29) (Chromosome 7 Open Reading Frame 29 (C7ORF29))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp C7orf29 est non-conjugé

Application: ELISA, 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)), Immunocytochemistry (ICC)

Détail du produit anti-C7orf29 anticorps

Épitope: AA 131-236

Homologie: Human

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human C7ORF29

Isotype: IgG

Information d'application

Indications d'application: WB 1:300-5000
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 C7orf29

Antigène: C7orf29 (C7ORF29) (Chromosome 7 Open Reading Frame 29 (C7ORF29))

Autre désignation: C7ORF29

Sujet:

Synonyms: C7orf29, CG029_HUMAN, Chromosome 7 open reading frame 29, Hypothetical protein LOC113763, Uncharacterized protein C7orf29.

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 C7orf29 gene product has been provisionally designated C7orf29 pending further characterization.

ID gène: 113763