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The rare aging disease Hutchinson-Gilford progeria is associated with the LMNA gene on chromosome 1 which encodes lamin A
Bioworld Molecular Weight: 35KDa
RRID: AB_2843002
DF12208-200
Extra Notes: Immunohistochemistry of paraffin-embedded mouse kidney using HGF Rabbit pAb at dilution of 1:50
SNX7 Polyclonal Antibody-BS71877 SiRNA Transfection The rare aging disease Hutchinson-GilfordSNX7 Polyclonal Antibody Sizes: 50 l, 100 l Catalogue Numbers: BS71877 50, BS71877 100 Product: 1mg ml in PBS with 0. 02% sodium azide, 50% glycerol, pH7. 2 Swiss Prot: Q9UNH6 Host: Rabbit Reactivity: Mouse, Rat Applications: WB All Applications: WB,1: 500 1: 2000 Background: This gene encodes a member of the sorting nexin family. Members of this family contain a phox (PX) domain, which is a phosphoinositide binding domain, and are involved in
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