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Anti-NUBPL TRUEMAB Antibody Clone OTI7D6

TrueMAB™ Antibodies - Made against Authentic Protein Antigens


Specifications Citations Customer Reviews Product Documents
SKU Description Amount Price Availability*  
TA503746 NUBPL mouse monoclonal antibody, clone OTI7D6 (formerly 7D6) 100ul 325
In Stock
LC410869 NUBPL HEK293T cell transient overexpression lysate (as WB positive control) 20ug $50 In Stock
CF503746 Carrier-free (BSA/glycerol-free) NUBPL mouse monoclonal antibody, clone OTI7D6 (formerly 7D6) 100ug $450 3-4 weeks
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OriGene Data

ImmunogenHuman recombinant protein fragment corresponding to amino acids 1-250 of human NUBPL(NP_079428) produced in E.coli.
Clone NameClone OTI7D6 IsotypeIgG1
Species ReactivityHuman Concentration0.75 mg/ml
Guaranteed Application *WB, FC Suggested DilutionsWB 1:2000, FLOW 1:100,
Predicted MW Explanation 33.9 kDa
BufferPBS (PH 7.3) containing 1% BSA, 50% glycerol and 0.02% sodium azide.
Purification Purified from mouse ascites fluids by affinity chromatography

Reference Data

Target NameHomo sapiens nucleotide binding protein-like (NUBPL), transcript variant 1
Alternative NameC14orf127; huInd1; IND1
Database LinkNP_079428
Entrez Gene 80224 Human
FunctionThis gene encodes a member of the Mrp/NBP35 ATP-binding proteins family. The encoded protein is required for the assembly of the respiratory chain NADH dehydrogenase (complex I), an oligomeric enzymatic complex located in the inner mitochondrial membrane. The respiratory complex I consists of 45 subunits and 8 iron-sulfur (Fe/S) clusters. This protein is an Fe/S protein that plays a critical role in the assembly of respiratory complex I, likely by transferring Fe/S into the Fe/S-containing complex I subunits. Mutations in this gene cause mitochondrial complex I deficiency. Alternatively spliced transcript variants encoding distinct isoforms have been identified.
Related Pathway

* Availability is in business days
* OriGene provides validated application data and protocol, with money back guarantee.

HEK293T cells were transfected with the pCMV6-ENTRY control (Left lane) or pCMV6-ENTRY NUBPL (RC204385, Right lane) cDNA for 48 hrs and lysed. Equivalent amounts of cell lysates (5 ug per lane) were separated by SDS-PAGE and immunoblotted with anti-NUBPL.
HEK293T cells transfected with either RC204385 overexpress plasmid(Red) or empty vector control plasmid(Blue) were immunostained by anti-NUBPL antibody(TA503746), and then analyzed by flow cytometry.


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