C7orf42 anticorps (AA 231-314) (Alexa Fluor 594)

N° du produit ABIN2810922

Détail du produit anti-C7orf42 anticorps (Alexa Fluor 594)

Antigène: C7orf42 (Chromosome 7 Open Reading Frame 42 (C7orf42))

Épitope: AA 231-314

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp C7orf42 est conjugé à/à la Alexa Fluor 594

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

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

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human C7orf42

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 C7orf42

Antigène: C7orf42 (Chromosome 7 Open Reading Frame 42 (C7orf42))

Autre désignation: C7orf42 (C7orf42 Produits)

Synonymes: anticorps C7orf42, anticorps c7orf42, anticorps TMEM248, anticorps MGC79534, anticorps C25H7orf42, anticorps 0610007L01Rik, anticorps A930023A16Rik, anticorps AW557951, anticorps G430067H08Rik, anticorps zgc:103561, anticorps transmembrane protein 248, anticorps transmembrane protein 248 L homeolog, anticorps TMEM248, anticorps tmem248.L, anticorps tmem248, anticorps Tmem248

Sujet:

Synonyms: C7orf42, TM248_HUMAN, Chromosome 7 open reading frame 42, FLJ10099, FLJ13090, Hypothetical protein LOC55069, UPF0458 protein C7orf42.

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 C7orf42 gene product has been provisionally designated C7orf42 pending further characterization.

ID gène: 55069