SLC26A4 Knockout Cell Lines

Gene: SLC26A4

Official Full Name: solute carrier family 26 member 4provided by HGNC

Gene Summary: Mutations in this gene are associated with Pendred syndrome, the most common form of syndromic deafness, an autosomal-recessive disease. It is highly homologous to the SLC26A3 gene; they have similar genomic structures and this gene is located 3' of the SLC26A3 gene. The encoded protein has homology to sulfate transporters. [provided by RefSeq, Jul 2008]

Get A Quote

Products

Catalog Number	Product Name	Species	Gene	Passage ratio	Mycoplasma testing	Price
KOA14374	SLC26A4 Knockout cell line (AC16)	Human	SLC26A4	1：3-1：4	negative	Online Inquiry
KOA29817	SLC26A4 Knockout cell line (BEAS-2B)	Human	SLC26A4	1:3~1:4	negative	Online Inquiry
KOA45245	SLC26A4 Knockout cell line (U-2932)	Human	SLC26A4	1：2-1：4	negative	Online Inquiry
KOA60629	SLC26A4 Knockout cell line (TPC-1)	Human	SLC26A4	1:5-1:8	negative	Online Inquiry
KOA76057	SLC26A4 Knockout cell line (NCM460)	Human	SLC26A4	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.