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CCDC164 Anticuerpo(N-14): sc-167338

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(Basado en el análisis de datos)
  • CCDC164 Antibody (N-14) is a goat polyclonal IgG provided at 200 µg/ml
  • epitope mapping near the N-terminus of CCDC164 of human origin
  • recommended for detection of CCDC164 of mouse, rat and human origin by WB, IF and ELISA
  • blocking peptide, sc-167338 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 
CCDC164 Antibody (N-14) sc-167338 200 µg/ml $279
CCDC164 (N-14) P sc-167338 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 C2orf39 92749 2p23.3 NM_145038 Q96MC2
 n/a
Ratón Gm1060 381738 5 B1 NM_001033460 Q3USS3
 No Disponible
 

The second largest human chromosome, 2 consists of 237 million bases encoding over 1,400 genes and making up approximately 8% of the human genome. A number of genetic diseases are linked to genes on chromosome 2. Harlequin icthyosis, a rare and morbid skin deformity, is associated with mutations in the ABCA12 gene. The lipid metabolic disorder sitosterolemia is associated with ABCG5 and ABCG8. An extremely rare recessive genetic disorder, Alström syndrome is due to mutations in the ALMS1 gene. Interestingly, chromosome 2 contains what appears to be a vestigial second centromere and vestigial telomeres which gives credence to the hypothesis that human chromosome 2 is the result of an ancient fusion of two ancestral chromosomes seen in modern form today in apes. The C2orf39 gene product has been provisionally designated C2orf39 pending further characterization.