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CCDC107 Anticuerpo(N-19): sc-242330

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(Basado en el análisis de datos)
  • CCDC107 Antibody (N-19) is a goat polyclonal IgG provided at 200 µg/ml
  • epitope mapping near the N-terminus of CCDC107 of human origin
  • recommended for detection of CCDC107 of human origin by WB, IF and ELISA
  • blocking peptide, sc-242330 P
 

Ver tambiénCCDC AntibodiesincluyebdoCCDC, CCDC103, CCDC106, CCDC113, CCDC120, CCDC121, CCDC128, CCDC135, CCDC136, CCDC137, CCDC140, CCDC144B, CCDC144NL, CCDC146, CCDC147, CCDC15, CCDC150, CCDC152, CCDC154, CCDC159, CCDC162, Ccdc163, CCDC21, CCDC22, CCDC23, CCDC27, CCDC28A, CCDC28B, CCDC3, CCDC30, CCDC39, CCDC41, CCDC42B, CCDC47, CCDC55, CCDC61, CCDC62, CCDC68, CCDC71, CCDC72, CCDC74A, CCDC74B, CCDC75, CCDC78, CCDC79, CCDC84, CCDC9, CCDC90, CCDC92, CCDC94, CCDC97, CCDC6, CCDC60, CCDC7, CCDC8, CCDC11, CCDC12, CCDC13, CCDC14, CCDC16, CCDC17, CCDC18, CCDC19, CCDC24, CCDC25, CCDC32, CCDC33, CCDC34, CCDC36, CCDC37, CCDC38, CCDC40, CCDC42, CCDC43, CCDC44, CCDC45, CCDC46, CCDC48, CCDC49, CCDC51, CCDC52, CCDC53, CCDC56, CCDC57, CCDC58, CCDC63, CCDC64, CCDC65, CCDC66, CCDC67, CCDC69, CCDC70, CCDC73, CCDC74, CCDC76, CCDC77, CCDC81, CCDC82, CCDC83, CCDC85, CCDC87, CCDC89, CCDC91, CCDC93, CCDC96, CCDC98, CCDC99, CCDC101, CCDC102, CCDC104, CCDC105, CCDC107, CCDC108, CCDC109, CCDC110, CCDC111, CCDC112, CCDC114, CCDC115, CCDC116, CCDC117, CCDC122, CCDC123, CCDC124, CCDC125, CCDC126, CCDC127, CCDC129, CCDC130, CCDC132, CCDC134, CCDC138, CCDC141, CCDC142, CCDC144A, CCDC148, CCDC149, CCDC151, CCDC153, CCDC155, CCDC157, CCDC164yCCDC167.

Información sobre pedidosInformación del gen
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 Información sobre pedidos
Nombre del productoNúmero de catálogoUnidadPrecioCantidadAñadir 
CCDC107 Antibody (N-19) sc-242330 200 µg/ml $279
CCDC107 (N-19) P sc-242330 P
(peptide)
 100 µg/0.5 ml $61
 
Especies Nombre del Gen Gene ID Ubicación en el cromosoma Numero de Acceso de Isoforma (ARNm) Número de Acceso de la Proteína Número OMIM™:
Humano CCDC107 203260 9p13.3 NM_174923 Q8WV48
 n/a
 

CCDC107 (coiled-coil domain containing 107) is a 283 amino acid single-pass membrane protein that exists as four alternatively spliced isoforms. The gene encoding CCDC107 maps to human chromosome 9p13.3. Chromosome 9 consists of about 145 million bases, represents 4% of the human genome and encodes nearly 900 genes. Thought to play a role in gender determination, deletion of the distal portion of 9p can lead to development of male to female sex reversal, the phenotype of a female with a male X,Y genotype. Hereditary hemorrhagic telangiectasia, which is characterized by harmful vascular defects, is associated with the chromosome 9 gene encoding endoglin protein, ENG. Familial dysautonomia is also associated with chromosome 9 though through the gene IKBKAP. Notably, chromosome 9 encompasses the largest interferon family gene cluster. Chromosome 9 is partnered with chromosome 22 in the translocation leading to the aberrant production of BCR-ABL fusion protein often found in leukemias.