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BS74169-100
Immunohistochemical analysis of MITF staining in human melanoma formalin fixed paraffin embedded tissue section
Calcium activated neutral proteinase
Usher syndrome 1D and nonsyndromic autosomal recessive deafness DFNB12 are caused by allelic mutations of this cadherin-like gene
Catalogue Numbers: NCP0162P-50
Thyroid Transcription Factor 1 Monoclonal Antibody-MB11734 primary and hard-to-transfect cells BS74169-100Thyroid Transcription Factor 1 Monoclonal Antibody Sizes: 50l, 100l Catalogue Numbers: MB11734 50, MB11734 100 Product: 50mM Tris Glycine(pH 7. 4), 0. 15M NaCl, 40% Glycerol, 0. 01% Sodium azide and 0. 05% BSA Swiss Prot: P43699 Host: Rabbit Reactivity: Human, Mouse, Rat Applications: WB, IHC P, IP, All Applications: WB: 1 500 1 1000 IHC: 1 50 1 100 IP: 1 20 Background: This gene encodes a protein initially identified as a thyroid specific
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