C2ORF61 anticorps (AA 21-120) (Cy3)

N° du produit ABIN1702813

Cet anticorps Lapin Polyclonal détecte spécifiquement C2ORF61 dans WB, IF (cc) et IF (p). Il présente une réactivité envers Humain.

Aperçu rapide pour C2ORF61 anticorps (AA 21-120) (Cy3) (ABIN1702813)

Antigène: C2ORF61 (Chromosome 2 Open Reading Frame 61 (C2ORF61))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp C2ORF61 est conjugé à/à la Cy3

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

Détail du produit anti-C2ORF61 anticorps (Cy3)

Épitope: AA 21-120

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

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human C2orf61

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 C2ORF61

Antigène: C2ORF61 (Chromosome 2 Open Reading Frame 61 (C2ORF61))

Autre désignation: C2orf61

Sujet:

Synonyms: CCDC113, Chromosome 2 open reading frame 61, Coiled-coil domain-containing protein 113 Gene names, DKFZp434N1418, HSPC065, Uncharacterized protein C2orf61, CB061_HUMAN.

Background: C2orf61 (chromosome 2 open reading frame 61), also known as FLJ40172, is a 177 amino acid protein encoded by a gene that maps to human chromosome 2p21. As the second largest human chromosome, chromosome 2 makes up approximately 8 % of the human genome and contains 237 million bases encoding over 1,400 genes. A number of genetic diseases are linked to genes on chromosome 2. Harlequin icthyosis, a rare skin deformity, is associated with mutations in the ABCA12 gene. The lipid metabolic disorder sitosterolemia is associated with ABCG5 and ABCG8. An extremely rare recessive genetic disorder, Alstr syndrome, is related to mutations in the ALMS1 gene. Chromosome 2 contains a probable vestigial second centromere as well as vestigial telomeres, which gives credence to the hypothesis that human chromosome 2 formed as a result of an ancient fusion of two ancestral chromosomes, which are still present in modern day apes.

ID gène: 285051