CCDC174 anticorps (AA 1-100) (Biotin)

N° du produit ABIN1700222

L’anticorps Lapin Polyclonal anti-CCDC174 a été validé pour WB, ELISA, IHC (fro) et IHC (p). Il convient pour détecter CCDC174 dans des échantillons de Humain.

Aperçu rapide pour CCDC174 anticorps (AA 1-100) (Biotin) (ABIN1700222)

Antigène: CCDC174 (Coiled-Coil Domain Containing 174 (CCDC174))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp CCDC174 est conjugé à/à la Biotin

Application: Western Blotting (WB), ELISA, Immunohistochemistry (Frozen Sections) (IHC (fro)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Détail du produit anti-CCDC174 anticorps (Biotin)

Épitope: AA 1-100

Homologie: Human,Mouse,Rat

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human C3orf19

Isotype: IgG

Information d'application

Indications d'application: WB 1:300-5000
IHC-P 1:200-400
IHC-F 1:100-500

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 for 12 months.

Date de péremption: 12 months

Détails sur CCDC174

Antigène: CCDC174 (Coiled-Coil Domain Containing 174 (CCDC174))

Autre désignation: C3orf19

Sujet:

Synonyms: Ccdc174, Coiled coil domain containing 174, Uncharacterized protein C3orf19, CC174_HUMAN.

Background: Chromosome 3 is made up of about 214 million bases encoding over 1,100 genes. Notably, there is a chemokine receptor gene cluster and a variety of human cancer related loci on chromosome 3. Particular regions of the chromosome 3 short arm are deleted in many types of cancer cells. Key tumor suppressing genes on chromosome 3 encode apoptosis mediator RASSF1, cell migration regulator HYAL1 and angiogenesis suppressor SEMA3B. Marfan Syndrome, porphyria, von Hippel-Lindau syndrome, osteogenesis imperfecta and Charcot-Marie-Tooth Disease are a few of the numerous genetic diseases associated with chromosome 3. The C3orf19 gene product has been provisionally designated C3orf19 pending further characterization.