CLDN19 Knockout Cell Lines

Gene: CLDN19

Official Full Name: claudin 19provided by HGNC

Gene 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]

Get A Quote

Products

Catalog Number	Product Name	Species	Gene	Passage ratio	Mycoplasma testing	Price
KOA04565	CLDN19 Knockout cell line (AC16)	Human	CLDN19	1：3-1：4	negative	Online Inquiry
KOA20010	CLDN19 Knockout cell line (BEAS-2B)	Human	CLDN19	1:3~1:4	negative	Online Inquiry
KOA35457	CLDN19 Knockout cell line (U-2932)	Human	CLDN19	1：2-1：4	negative	Online Inquiry
KOA50864	CLDN19 Knockout cell line (TPC-1)	Human	CLDN19	1:5-1:8	negative	Online Inquiry
KOA66270	CLDN19 Knockout cell line (NCM460)	Human	CLDN19	1:2~1:3	negative	Online Inquiry

Please note that all services are for research use only. Not intended for any clinical use.

Get a free quote

If your question is not addressed through these resources, you can fill out the online form below and we will answer your question as soon as possible.