蛋白
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检测试剂盒
蛋白MARKER
分子生物学
规格：
查看说明书Recombinant Human NADH dehydrogenase [ubiquinone] iron-sulfur protein 4, mitochondrial(NDUFS4)
Cat#:TP03131应用：Positive Control; Immunogen; SDS-PAGE; WB
| Product Name: | Ndufs4 Rabbit pAb |
| Cat No.: | DPA03928 |
| Clonality: | Polyclonal |
| Species Reactivity: | Human, Mouse, Rat |
| Tested Applications: | WB,IHC,ICC/IF,FC,IP |
| Recommended Dilution: | WB: 1:1000 IHC: 1:20-1:50 ICC/IF: 1:20-1:50 FC: 1:20-1:100 IP: 1:20-1:50 |
| 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 Ndufs4 |
| Calculated Molecular Weight: | 20 kDa |
| Observed Molecular Weight: | 20 kDa |
| GenBank Accession Number: | O43181 |
| Gene ID (NCBI): | 4724 |
| Synonyms: | AQDQ; CI-18; CI-AQDQ; CI-18 kDa |
| Background: | This gene encodes an nuclear-encoded accessory subunit of the mitochondrial membrane respiratory chain NADH dehydrogenase (complex I, or NADH:ubiquinone oxidoreductase). Complex I removes electrons from NADH and passes them to the electron acceptor ubiquinone. Mutations in this gene can cause mitochondrial complex I deficiencies such as Leigh syndrome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2015] |
| Category: | Primary Ab |
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