C12ORF24 anticorps (AA 195-245) (Alexa Fluor 680)

N° du produit ABIN4997887

Détail du produit anti-C12ORF24 anticorps (Alexa Fluor 680)

Antigène: C12ORF24 (C12orf24) (Chromosome 12 Open Reading Frame 24 (C12orf24))

Épitope: AA 195-245

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp C12ORF24 est conjugé à/à la Alexa Fluor 680

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

Réactivité croisée: Humain, Souris, Rat

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human C12ORF24

Isotype: IgG

Information d'application

Indications d'application: IF(IHC-P) 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 C12ORF24

Antigène: C12ORF24 (C12orf24) (Chromosome 12 Open Reading Frame 24 (C12orf24))

Autre désignation: C12ORF24 (C12orf24 Produits)

Synonymes: anticorps C12orf24, anticorps C17H12orf24, anticorps HSU79274, anticorps 1500011H22Rik, anticorps family with sequence similarity 216 member A, anticorps family with sequence similarity 216, member A, anticorps FAM216A, anticorps Fam216a

Sujet:

Synonyms: Chromosome 12 open reading frame 24, HSU79274, Hypothetical protein LOC29902, Protein predicted by clone 23733, F216A_HUMAN, Protein FAM216A, FAM216A.

Background: Encoding over 1,100 genes within 132 million bases, chromosome 12 makes up about 4.5 % of the human genome. A number of skeletal deformities are linked to chromosome 12 including hypochondrogenesis, achondrogenesis and Kniest dysplasia. Noonan syndrome, which includes heart and facial developmental defects among the primary symptoms, is caused by a mutant form of PTPN11 gene product, SH-PTP2. Chromosome 12 is also home to a homeobox gene cluster which encodes crucial transcription factors for morphogenesis, and the natural killer complex gene cluster encoding C-type lectin proteins which mediate the NK cell response to MHC I interaction. Trisomy 12p leads to facial development defects, seizure disorders and a host of other symptoms varying in severity depending on the extent of mosaicism and is most severe in cases of complete trisomy. The C12orf24 gene product has been provisionally designated C12orf24 pending further characterization.

ID gène: 29902

UniProt: Q8WUB2