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ND4L (T-15) 抗体: sc-20501

 |  データシート
  • goat polyclonal IgG, 200 µg/ml
  • epitope mapping within an internal region of ND4L of human origin
  • recommended for detection of NADH-ubiquinone oxidoreductase chain 4L of human origin by WB, IF and ELISA
  • blocking peptide, sc-20501 P
 
Additional ND 抗体 ...
 
注文情報
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WB   IF  
 
Species 遺伝子名 Gene ID Chromosome Location Isoform (mRNA) Accession # Protein Accession # OMIM™ Number
ヒト MT-ND4L 4539 MT P03901
n/a
 
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 注文情報
製品名カタログ #Unit価格数量追加Favorites
ND4L (T-15) sc-20501 200 µg/ml $279
ND4L (T-15) P sc-20501 P
(peptide)
100 µg/0.5 ml $61
 WB Positive Control Cell Lysates (click product name for more information)
製品名カタログ #Unit価格数量追加Favorites
THP-1 Cell Lysate sc-2238 500 µg/200 µl $104
HL-60 Whole Cell Lysate sc-2209 500 µg/200 µl $104
 WB Control Recombinant Protein (click product name for more information)
製品名カタログ #Unit価格数量追加Favorites
c-Fms/CSF-1R (11-310) sc-4339 WB 10 µg/0.1 ml $88

ND4L Background Information
NADH:ubiquinone oxidoreductase (complex I) is an extremely complicated multiprotein complex located in the inner mitochondrial membrane. Human complex I is important for energy metabolism because its main function is to transport electrons from NADH to ubiquinone, which is accompanied by translocation of protons from the mitochondrial matrix to the intermembrane space. Human complex I appears to consist of 41 subunits. A small number of complex I subunits are the products of mitochondrial genes (subunits 1-7), while the remainder are nuclear encoded and imported from the cytoplasm. NADH dehydrogenase subunit 4L (ND4L) is most likely a component of the hydrophobic protein fragment of Complex I. Mutations in the gene encodiing for ND4 are implicated in Leber hereditary optic neuropathy, a rare condition that can cause loss of central vision.