C2orf24 anticorps

N° du produit ABIN1387180

Détail du produit anti-C2orf24 anticorps

Antigène: C2orf24 (Chromosome 2 Open Reading Frame 24 (C2orf24))

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp C2orf24 est non-conjugé

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

Réactivité croisée: Humain, Souris, Rat

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human C2orf24

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 C2orf24

Antigène: C2orf24 (Chromosome 2 Open Reading Frame 24 (C2orf24))

Autre désignation: C2orf24 (C2orf24 Produits)

Synonymes: anticorps c2orf24, anticorps wu:fa05h07, anticorps zgc:55857, anticorps MGC75999, anticorps C12H2orf24, anticorps MGC115028, anticorps DKFZp459J1014, anticorps C2orf24, anticorps CGI-57, anticorps C2H2orf24, anticorps C7H2orf24, anticorps 1810031K17Rik, anticorps AU043960, anticorps RGD735175, anticorps cyclin Pas1/PHO80 domain containing 1, anticorps cyclin Pas1/PHO80 domain containing 1 L homeolog, anticorps cnppd1, anticorps CNPPD1, anticorps cnppd1.L, anticorps Cnppd1

Sujet:

Synonyms: CDABP0125, CGI 57, chromosome 2 open reading frame 24, CNPD1_HUMAN, CNPPD1, Cyclin Pas1/PHO80 domain-containing protein 1, Protein CNPPD1.

Background: The second largest human chromosome, 2 consists of 237 million bases encoding over 1,400 genes and making up approximately 8 % of the human genome. A number of genetic diseases are linked to genes on chromosome 2. Harlequin icthyosis, a rare and morbid 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 due to mutations in the ALMS1 gene. Interestingly, chromosome 2 contains what appears to be a vestigial second centromere and vestigial telomeres which gives credence to the hypothesis that human chromosome 2 is the result of an ancient fusion of two ancestral chromosomes seen in modern form today in apes. The C2orf24 gene product has been provisionally designated C2orf24 pending further characterization.

ID gène: 27013