HYDIN Knockout Cell Lines

Gene: HYDIN

Official Full Name: HYDIN axonemal central pair apparatus proteinprovided by HGNC

Gene Summary: This gene encodes a protein that may be involved in cilia motility. Mutations in this gene cause of autosomal recessive primary ciliary dyskinesia-5, a disorder characterized by the accumulation of cerebrospinal fluid within the ventricles of the brain. A duplicate copy of this gene has been found in humans on chromosome 1. [provided by RefSeq, Jan 2013]

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Products

Catalog Number	Product Name	Species	Gene	Passage ratio	Mycoplasma testing	Price
KOA09091	HYDIN Knockout cell line (AC16)	Human	HYDIN	1：3-1：4	negative	Online Inquiry
KOA24536	HYDIN Knockout cell line (BEAS-2B)	Human	HYDIN	1:3~1:4	negative	Online Inquiry
KOA39982	HYDIN Knockout cell line (U-2932)	Human	HYDIN	1：2-1：4	negative	Online Inquiry
KOA55373	HYDIN Knockout cell line (TPC-1)	Human	HYDIN	1:5-1:8	negative	Online Inquiry
KOA70789	HYDIN Knockout cell line (NCM460)	Human	HYDIN	1:2~1:3	negative	Online Inquiry

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

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