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规格：
查看说明书Recombinant Human NDUFAF1 Protein
Cat#:TP03125应用：Positive Control; Immunogen; SDS-PAGE; WB
| Product Name: | NDUFAF1 Rabbit pAb |
| Cat No.: | DPA05112 |
| Clonality: | Polyclonal |
| Species Reactivity: | Human, Mouse, Rat |
| Tested Applications: | WB,IHC,ICC/IF,FC,IP |
| Recommended Dilution: | WB: 1:2000-1:10000 IHC: 1:20-1:100 ICC/IF: 1:20-1:100 FC: 1:50 IP: 1:20 |
| Size: | 30ul 50ul 100uL |
| Format: | Liquid |
| Source: | Rabbit |
| Purification Method: | Affinity Purification |
| Isotype: | IgG |
| Conjugate: | Un-conjugated |
| Storage: | Store at -20°C. Supplied in 50nM Tris-Glycine(pH 7.4), 0.15M NaCl, 40%Glycerol, 0.01% sodium azide a |
| Immunogen: | A synthetic peptide of human NDUFAF1 |
| Calculated Molecular Weight: | 38 kDa |
| Observed Molecular Weight: | 35 kDa |
| GenBank Accession Number: | Q9Y375 |
| Gene ID (NCBI): | 51103 |
| Synonyms: | CGI65; CIA30; CGI-65 |
| Background: | This gene encodes a complex I assembly factor protein. Complex I (NADH-ubiquinone oxidoreductase) catalyzes the transfer of electrons from NADH to ubiquinone (coenzyme Q) in the first step of the mitochondrial respiratory chain, resulting in the translocation of protons across the inner mitochondrial membrane. The encoded protein is required for assembly of complex I, and mutations in this gene are a cause of mitochondrial complex I deficiency. Alternatively spliced transcript variants have been observed for this gene, and a pseudogene of this gene is located on the long arm of chromosome 19. [provided by RefSeq, Dec 2011] |
| Category: | Primary Ab |
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