CLDN19
claudin 19
别名:
HOMG5 
物种:
Human CLDN19 (149461), Mouse Cldn19 (242653), Rat Cldn19 (298487), sheep CLDN19 (101102362), domestic guinea pig Cldn19 (100714164), cow CLDN19 (513034), dog CLDN19 (607005), naked mole-rat Cldn19 (101725162), Horse CLDN19 (100053591), Zebrafish cldn19 (550431) 
UniProtKB ID:
基因ID:
- Human(149461) Summary: The product of this gene belongs to the claudin family. It plays a major role in tight junction-specific obliteration of the intercellular space, through calcium-independent cell-adhesion activity. Defects in this gene are the cause of hypomagnesemia renal with ocular involvement (HOMGO). HOMGO is a progressive renal disease characterized by primary renal magnesium wasting with hypomagnesemia, hypercalciuria and nephrocalcinosis associated with severe ocular abnormalities such as bilateral chorioretinal scars, macular colobomata, significant myopia and nystagmus. Alternatively spliced transcript variants encoding distinct isoforms have been identified for this gene. [provided by RefSeq, Jun 2010]
- Mouse(242653) claudin 19
- Rat(298487) claudin 19
- sheep(101102362) claudin 19
- domestic guinea pig(100714164) claudin 19
- cow(513034) claudin 19
- dog(607005) claudin 19
- naked mole-rat(101725162) claudin 19
- Horse(100053591) claudin 19
- Zebrafish(550431) claudin 19
- domestic cat(101093875) claudin 19
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Antibodies
产品编号
说明
物种反应性
应用
Anti-Cldn19 Antibody Produced In Rabbit, Prestige Antibodies® Powered by Atlas Antibodies, affinity isolated antibody, buffered aqueous glycerol solution, 
物种反应性
human 
应用
immunofluorescence
esiRNA
产品编号
说明
物种