C7ORF26 anticorps (AA 1-100) (Alexa Fluor 555)

N° du produit ABIN1696918

Détail du produit anti-C7ORF26 anticorps (Alexa Fluor 555)

Antigène: C7ORF26 (Chromosome 7 Open Reading Frame 26 (C7ORF26))

Épitope: AA 1-100

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp C7ORF26 est conjugé à/à la Alexa Fluor 555

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

Homologie: Human,Mouse,Rat,Dog,Cow,Chicken,Rabbit

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human C7orf26

Isotype: IgG

Information d'application

Indications d'application: IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200

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, 0.03 % 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. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

Date de péremption: 12 months

Détails sur C7ORF26

Antigène: C7ORF26 (Chromosome 7 Open Reading Frame 26 (C7ORF26))

Autre désignation: C7orf26 (C7ORF26 Produits)

Synonymes: anticorps C14H7orf26, anticorps zgc:77458, anticorps c7orf26, anticorps chromosome 7 open reading frame 26, anticorps chromosome 14 C7orf26 homolog, anticorps zgc:56409, anticorps chromosome 7 open reading frame 26 L homeolog, anticorps chromosome 25 open reading frame, human C7orf26, anticorps C7orf26, anticorps C14H7orf26, anticorps zgc:56409, anticorps c7orf26.L, anticorps C25H7orf26

Sujet:

Synonyms: Chromosome 7 open reading frame 26, MGC2718, Uncharacterized protein C7orf26,CG026_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 C7orf26 gene product has been provisionally designated C7orf26 pending further characterization.