Cdh23 RT-PCR Gene Expression Assay - GXD

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Gene Expression Data
Assay Details

Assay

Reference:	J:66698 Di Palma F, et al., Mutations in cdh23, encoding a new type of cadherin, cause stereocilia disorganization in waltzer, the mouse model for usher syndrome type 1D. Nat Genet. 2001 Jan;27(1):103-7
Assay type:	RT-PCR
MGI Accession ID:	MGI:2654806
Gene symbol:	Cdh23
Gene name:	cadherin related 23 (otocadherin)

Probe:

EB9.F, EB.21R

Results

Image: 2e set A ©

	Sample Information		Bands		Other Sample Information
Lane	Age	Structure	577 bp (a)	458 bp (b)	Amount	Genetic Background	Mutant Allele(s)	Sex
+/+	P	TS28: brain	Present	Not Applicable	.4 µg; total RNA	C57BL/6		Not Specified
+/V^Alb	P	TS28: brain	Present	Present	.4 µg; total RNA	involves: C3H/HeJ * C57BL/6	Cdh23^v-Alb/Cdh23⁺	Not Specified
V^Alb/V^Alb	P	TS28: brain	Absent	Present	.4 µg; total RNA	involves: C3H/HeJ * C57BL/6	Cdh23^v-Alb/Cdh23^v-Alb	Not Specified
+/+	Lane not used in this assay
+/V^Alb	Lane not used in this assay
V^Alb/V^Alb	Lane not used in this assay

Notes:
(a) This band is the transcript from the wild type allele.
(b) This band is the transcript from the mutant allele.

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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