ArtNr |
PRS-27-185-100ul |
Hersteller |
ProSci
|
Menge |
100 ul |
Kategorie |
|
Typ |
Antibody Polyclonal |
Format |
Liquid |
Applikationen |
WB, ELISA |
Specific against |
Human |
Host |
Rabbit |
ECLASS 10.1 |
32160702 |
ECLASS 11.0 |
32160702 |
UNSPSC |
12352203 |
Alias |
TUFM, COXPD4, EF-TuMT, EFTU, P43 |
Lieferbar |
|
Shipping |
blue ice or RT |
Immunogen |
Antibody produced in rabbits immunized with a synthetic peptide corresponding a region of human TUFM. |
Applications |
TUFM antibody can be used for detection of TUFM by ELISA at 1:1562500. TUFM antibody can be used for detection of TUFM by western blot at 1 μ g/mL, and HRP conjugated secondary antibody should be diluted 1:50, 000 - 100, 000. |
Positive Control 1 |
Cat. No. 1201 - HeLa Cell Lysate |
Predicted Molecular Weight |
50 kDa |
Purification |
Antibody is purified by peptide affinity chromatography method. |
Clonality |
Polyclonal |
Conjugate |
Unconjugated |
Buffer |
Purified antibody supplied in 1x PBS buffer with 0.09% (w/v) sodium azide and 2% sucrose. |
Concentration |
batch dependent |
Storage Conditions |
For short periods of storage (days) store at 4˚ C. For longer periods of storage, store TUFM antibody at -20˚ C. As with any antibody avoid repeat freeze-thaw cycles. |
Disclaimer |
This product is for research use only. |
Modifications |
None |
Ncbi Official Symbol |
TUFM |
Accession # |
NP_003312 |
Protein Gi # |
34147630 |
Ncbi Gene Id # |
7284 |
User Note |
Optimal dilutions for each application to be determined by the researcher. |
Ncbi Official Symbol |
TUFM |
Ncbi Official Full Name |
Tu translation elongation factor, mitochondrial |
Ncbi Organism |
Homo sapiens |
Swissprot # |
P49411 |
Background |
TUFM is a protein which participates in protein translation in mitochondria. Mutations in this gene have been associated with combined oxidative phosphorylation deficiency resulting in lactic acidosis and fatal encephalopathy. This gene encodes a protein which participates in protein translation in mitochondria. Mutations in this gene have been associated with combined oxidative phosphorylation deficiency resulting in lactic acidosis and fatal encephalopathy. A pseudogene has been identified on chromosome 17. Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Entrez Gene record to access additional publications. |
Background References 1 |
Valente, L., (2007) Am. J. Hum. Genet. 80 (1), 44-58. |
1st Image Caption |
Antibody used in WB on Human HeLa at 0.2-1 ug/ml. |
2nd Image Caption |
Antibody used in WB on Hum. Fetal Lung at 1 ug/ml. |
Hinweis: Die dargestellten Informationen und Dokumente (Bedienungsanleitung, Produktdatenblatt, Sicherheitsdatenblatt und Analysezertifikat) entsprechen unserem letzten Update und sollten lediglich der Orientierung dienen. Wir übernehmen keine Garantie für die Aktualität. Für spezifische Anforderungen bitten wir Sie, uns eine Anfrage zu stellen.
Alle Produkte sind nur für Forschungszwecke bestimmt. Nicht für den menschlichen, tierärztlichen oder therapeutischen Gebrauch.