C12ORF29 anticorps (Alexa Fluor 750)

N° du produit ABIN4997890

Détail du produit anti-C12ORF29 anticorps (Alexa Fluor 750)

Antigène: C12ORF29 (Chromosome 12 Open Reading Frame 29 (C12ORF29))

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp C12ORF29 est conjugé à/à la Alexa Fluor 750

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 C12ORF29

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 C12ORF29

Antigène: C12ORF29 (Chromosome 12 Open Reading Frame 29 (C12ORF29))

Autre désignation: C12ORF29 (C12ORF29 Produits)

Synonymes: anticorps C12orf29, anticorps 4930571E09Rik, anticorps A730088G13Rik, anticorps AW551239, anticorps C430008C19Rik, anticorps chromosome 12 open reading frame 29, anticorps chromosome 5 open reading frame, human C12orf29, anticorps chromosome 3 open reading frame, human C12orf29, anticorps RIKEN cDNA 4930430F08 gene, anticorps C12orf29, anticorps C5H12orf29, anticorps C3H12orf29, anticorps 4930430F08Rik

Sujet:

Synonyms: CL029_HUMAN, Uncharacterized protein C12orf29.

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 C12orf29 gene product has been provisionally designated C12orf29 pending further characterization.

ID gène: 91298