C12ORF29 anticorps (N-Term)

N° du produit ABIN951538

Cet anticorps Lapin Polyclonal détecte spécifiquement C12ORF29 dans WB, FACS, IF, IHC (p) et EIA. Il présente une réactivité avec des échantillons de Humain et Souris.

Aperçu rapide pour C12ORF29 anticorps (N-Term) (ABIN951538)

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

Reactivité: Humain, Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp C12ORF29 est non-conjugé

Application: Western Blotting (WB), Flow Cytometry (FACS), Immunofluorescence (IF), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Enzyme Immunoassay (EIA)

Détail du produit anti-C12ORF29 anticorps

Épitope: AA 68-96, N-Term

Specificité: This antibody recognizes CL029 (N-term)

Réactivité croisée (Details): Species reactivity (tested):Human, Mouse.

Purification: Peptide Affinity Chromatography on Protein A

Immunogène: KLH conjugated synthetic peptide between 68-96 amino acids from the N-terminal region of Human CL029 Genename: C12orf29

Isotype: Ig Fraction

Information d'application

Indications d'application: Optimal working dilution should be determined by the investigator.

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 0.25 mg/mL

Buffer: PBS, 0.09 % (W/V) Sodium Azide

Agent conservateur: Sodium azide

Précaution d'utilisation: This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Conseil sur la manipulation: Avoid repeated freezing and thawing.

Stock: 4 °C/-20 °C

Stockage commentaire: Store the antibody undiluted at 2-8 °C for one month or (in aliquots) at -20 °C for longer.

Détails sur C12ORF29

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

Autre désignation: C12orf29

Sujet: 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.

Poids moléculaire: 37490 Da

ID gène: 91298

NCBI Accession: NP_001009894