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Immunofluorescent analysis of C20orf7 showing staining in the cytoplasm of SK-N-SH cells. SK-N-SH cells were fixed in 2% paraformaldehyde/culture medium at 37°C for 30 min and stained using a C20orf7 polyclonal antibody (Product # PA5-31396) diluted at 1:500. Blue: Hoechst 33342 staining.
|Tested species reactivity||Human|
|Host / Isotype||Rabbit / IgG|
|Immunogen||Recombinant fragment corresponding to a region within amino acids 141 and 345 of Human C20orf7|
|Purification||Antigen affinity chromatography|
|Storage buffer||0.1M tris glycine, pH 7, with 20% glycerol|
|Storage Conditions||-20° C, Avoid Freeze/Thaw Cycles|
|Tested Applications||Dilution *|
|Immunohistochemistry (Paraffin) (IHC (P))||1:100-1:1000|
|Western Blot (WB)||1:500-1:3000|
* Suggested working dilutions are given as a guide only. It is recommended that the user titrate the product for use in their own experiment using appropriate negative and positive controls.
PA5-31396 targets C20orf7 in IHC (P) and WB applications and shows reactivity with Human samples.
The PA5-31396 immunogen is recombinant fragment corresponding to a region within amino acids 141 and 345 of Human C20orf7.
The NADH-ubiquinone oxidoreductase complex (complex I) of the mitochondrial respiratory chain catalyzes the transfer of electrons from NADH to ubiquinone, and consists of at least 43 subunits. The complex is located in the inner mitochondrial membrane. This gene encodes a mitochondrial protein that is associated with the matrix face of the mitochondrial inner membrane and is required for complex I assembly. A mutation in this gene results in mitochondrial complex I deficiency. Multiple transcript variants encoding different isoforms have been found for this gene.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
bA526K24.2; dJ842G6.1; mitochondrial; NADH dehydrogenase (ubiquinone) complex I, assembly factor 5; NADH dehydrogenase [ubiquinone] 1 alpha subcomplex assembly factor 5; probable methyltransferase C20orf7; Probable methyltransferase C20orf7, mitochondrial
bA526K24.2; C20orf7; dJ842G6.1; NDUFAF5