Kallman Syndrome (KS) Detection Assay: A Molecular Tool for Early Diagnosis

Kallman syndrome (KS) detection assay

Technology	FISH	ISH
Kallman syndrome (KS) detection assay
Application	Microdeletion syndrome	Microdeletion syndrome
Area of interest	Fixed cytological specimen	Fixed cytological specimen
Region	Xp11.1-q11.1 and Xp22.31	Xp11.1-q11.1 and Xp22.31
Label	♦ (AF488, 2000) and ♦(AF555, 3000)	Biotin (0100) and Digoxigenin (9900)
Product No.	C803K.2030.05	C803K.0199.05
	C803K.2030.10	C803K.0199.10
Product Type	In vitro diagnostics (IVD) or Research use only (RUO)	Research use only (RUO)
Intended Use	The REMBRANDT® Kallmann syndrome (KS) FISH detection assay is able to detect a deletion in the Kallmann syndrome critical region Xp22.31, in comparison to the centromeric region of the human chromosome X, by means of direct in situ hybridization	The Rembrandt® LSI Xp22.31/CEP X-ISH detection assay is intended to detect the Xp22.31 locus, in comparison to the centromeric region of chromosome X.
Kit contents	C803P.2030 LSI Xp22.31/CEP X-FISH probe mix	C803P.0199 LSI Xp22.31/CEP X-ISH probe mix
	R018R.0000 Pepsin diluent	R018R.0000 Pepsin diluent
	R011R.0000 Pepsin powder	R011R.0000 Pepsin powder
	R025R.0000 PanWash 4, 25x SSC	R025R.0000 PanWash 4, 25x SSC
	Z000R.0050 Fluorescent mounting medium

Catalog No.	Kallman syndrome (KS) detection assay

C803K.2030.05	REMBRANDT® Kallman syndrome (KS) FISH detection assay
C803K.2030.10	REMBRANDT® Kallman syndrome (KS) FISH detection assay
C803K.0199.05	REMBRANDT® LSI Xp22.31/CEP X ISH detection assay
C803K.0199.10	REMBRANDT® LSI Xp22.31/CEP X ISH detection assay

Products