NUBPL anticorps (AA 1-250)
-
- Antigène Voir toutes NUBPL Anticorps
- NUBPL (Nucleotide Binding Protein-Like (NUBPL))
-
Épitope
- AA 1-250
-
Reactivité
- Humain
-
Hôte
- Souris
-
Clonalité
- Monoclonal
-
Conjugué
- Cet anticorp NUBPL est non-conjugé
-
Application
- Western Blotting (WB), Flow Cytometry (FACS)
- Attributs du produit
- Homo sapiens nucleotide binding protein-like (NUBPL), transcript variant 1
- Purification
- Purified from mouse ascites fluids by affinity chromatography
- Immunogène
- Human recombinant protein fragment corresponding to amino acids 1-250 of human NUBPL(NP_079428) produced in E.coli.
- Clone
- 2C8
- Isotype
- IgG1
- Top Product
- Discover our top product NUBPL Anticorps primaire
-
-
- Indications d'application
- WB 1:2000, FLOW 1:100,
- Commentaires
-
The concentration of the product may vary between diferrent lots.
- Restrictions
- For Research Use only
-
- Format
- Liquid
- Concentration
- 0.5-1.0 mg/mL
- Buffer
- PBS (PH 7.3) containing 1 % BSA, 50 % glycerol and 0.02 % sodium azide.
- Agent conservateur
- Sodium azide
- Précaution d'utilisation
- This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- Stock
- -20 °C
-
- Antigène
- NUBPL (Nucleotide Binding Protein-Like (NUBPL))
- Autre désignation
- NUBPL (NUBPL Produits)
- Synonymes
- anticorps C14orf127, anticorps IND1, anticorps huInd1, anticorps 2410170E07Rik, anticorps nucleotide binding protein like, anticorps nucleotide binding protein-like, anticorps NUBPL, anticorps Nubpl
- Sujet
- This 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.
- Poids moléculaire
- 33.9 kDa
- ID gène
- 80224
- NCBI Accession
- NM_025152
- HGNC
- 80224
-