TMEM70 Antibody

ProSci
Product Code: PSI-5645
Product Group: Primary Antibodies
Supplier: ProSci
CodeSizePrice
PSI-5645-0.02mg0.02mg£150.00
Quantity:
PSI-5645-0.1mg0.1mg£449.00
Quantity:
Prices exclude any Taxes / VAT

Overview

Host Type: Rabbit
Antibody Isotype: IgG
Antibody Clonality: Polyclonal
Regulatory Status: RUO
Applications:
  • Enzyme-Linked Immunosorbent Assay (ELISA)
  • Immunofluorescence (IF)
  • Immunohistochemistry (IHC)
  • Western Blot (WB)

Images

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Western blot analysis of TMEM70 in human liver tissue lysate with TMEM70 antibody at 1 μg/mL.
2 / 3
Immunohistochemistry of TMEM70 in rat liver tissue with TMEM70 antibody at 5 μg/mL.
3 / 3
Immunofluorescence of TMEM70 in rat liver tissue with TMEM70 antibody at 20 μg/mL.

Western blot analysis of TMEM70 in human liver tissue lysate with TMEM70 antibody at 1 μg/mL.
Immunohistochemistry of TMEM70 in rat liver tissue with TMEM70 antibody at 5 μg/mL.
Immunofluorescence of TMEM70 in rat liver tissue with TMEM70 antibody at 20 μg/mL.

Further Information

Additional Names:
TMEM70 Antibody: MC5DN2, Transmembrane protein 70, mitochondrial
Application Note:
TMEM70 antibody can be used for detection of TMEM70 by Western blot at 1 μg/mL. Antibody can also be used for immunohistochemistry starting at 5 μg/mL. For immunofluorescence start at 20 μg/mL.

Antibody validated: Western Blot in human samples; Immunohistochemistry in rat samples and Immunofluorescence in rat samples. All other applications and species not yet tested.
Background:
TMEM70 Antibody: TMEM70 is a recently identified mitochondrial protein that is thought to play a role in the biogenesis of the ATP synthase in higher eukaryotes. Mutations in this gene result in early neonatal onset of hypotonia, hypertrophic cardiomyopathy, lactic acidos and 3-methylglutaconic aciduria (3-MGC-uria), and usually cause death within the first six weeks of life, although some patients survive much longer. Little is known of the role of TMEM70, but it is conserved across multicellular eukaryotic organisms. It contains a conserved DUF1301 domain and two putative transmembrane regions.
Background References:
  • Cizkova A, Stranecky V, Mayr JA, et al. TMEM70 mutations cause isolated ATP synthase deficiency and neonatal mitochondrial encephalocardiomyopathy. Nat. Genet.2008; 11:1288-90.
  • Honzik T, Tesarova M, Mayr JA, et al. Mitochondrial encephalocardio-myopathy with early neonatal onset due to TMEM70 mutation. Arch. Dis. Child.2010; 95:296-301.
  • Houstek J, Kmoch S, and Zeman J. TMEM70 protein - a novel ancillary factor of mammalian ATP synthase. Biochim. Biophys. Acta2009; 1787:529-32.
Buffer:
TMEM70 Antibody is supplied in PBS containing 0.02% sodium azide.
Concentration:
1 mg/mL
Conjugate:
Unconjugated
DISCLAIMER:
Optimal dilutions/concentrations should be determined by the end user. The information provided is a guideline for product use. This product is for research use only.
Homology:
Predicted species reactivity based on immunogen sequence: Bovine: (93%)
Immunogen:
TMEM70 antibody was raised against a 14 amino acid synthetic peptide near the center of human TMEM70.

The immunogen is located within amino acids 150 - 200 of TMEM70.
NCBI Gene ID #:
54968
NCBI Official Name:
transmembrane protein 70
NCBI Official Symbol:
TMEM70
NCBI Organism:
Homo sapiens
Physical State:
Liquid
Protein Accession #:
NP_060336
Protein GI Number:
34147498
Purification:
TMEM70 Antibody is affinity chromatography purified via peptide column.
Research Area:
Homeostasis
Swissprot #:
Q9BUB7
User NOte:
Optimal dilutions for each application to be determined by the researcher.

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