C2orf68 anticorps

N° du produit ABIN1385957

L’anticorps Lapin Polyclonal anti-C2orf68 a été validé pour WB, IF (p) et IHC (p). Il convient pour détecter C2orf68 dans des échantillons de Humain, Souris et Rat.

Aperçu rapide pour C2orf68 anticorps (ABIN1385957)

Antigène: C2orf68 (Chromosome 2 Open Reading Frame 68 (C2orf68))

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp C2orf68 est non-conjugé

Application: Western Blotting (WB), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Détail du produit anti-C2orf68 anticorps

Réactivité croisée: Humain, Souris, Rat

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human C2orf68

Isotype: IgG

Information d'application

Indications d'application: WB 1:300-5000
IHC-P 1:200-400
IF(IHC-P) 1:50-200

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 C2orf68

Antigène: C2orf68 (Chromosome 2 Open Reading Frame 68 (C2orf68))

Autre désignation: C2orf68

Sujet:

Synonyms: Chromosome 2 open reading frame 68, FLJ14112, FLJ35653, MGC131675, CB068_HUMAN.

Background: C2orf68, also known as FLJ14112, FLJ35653 or MGC131675, is a 168 amino acid protein belonging to the UPF0561 family. Existing as two alternatively spliced isoforms, C2orf68 is encoded by a gene that maps to human chromosome 2q11.2. 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.