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TMEM70 Antibodies

AND TMEM70 ELISA kits, TMEM70 Proteins

Many biological assays use antibodies to detect TMEM70, such as Western Blot (WB), ELISA, Flow Cytometry, Immunocytochemistry (IHC). These antibodies can be polyclonal or monoclonal, and react with TMEM70 in Human, Mouse, Rat, and many other animal samples. Boster Bio use mainly mouse and rabbit to develop TMEM70 antibodies...

We validate the specificity of these antibodies to TMEM70 by testing them on tissues known to express TMEM70 positively and negatively. Browse below to find the TMEM70 antibody that suites your experiment. We have 3 of these antibodies and many publications and validation images.

If you cannot find antibodies that fit your needs, contact us for making custom antibodies. We have a full suite of custom antibody services covering from research to diagnostic and therapeutic applications.

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TMEM70 Infographic by Boster Bio

All TMEM70 Products

Product

Figures

Specificity

Applications

Price

Anti-TMEM70 Antibody

Human, Mouse, Rat

ELISA, IF, IHC-P, WB

$449
Cat # A06360
0.1 mg

TMEM70 (NM_017866) Human Recombinant Protein

$1249
Cat # PROTQ9BUB7
20 µg

TMEM70 (NM_017866) Human Over-expression Lysate

Human

$628
Cat # LS054968
100 µg

TMEM70 Overview

Facts about Transmembrane protein 70, mitochondrial.

TMEM70 3D structure

TMEM70 3D structure. Source: alphafold

Transmembrane protein 70, mitochondrial (TMEM70)

Involved in biogenesis of mitochondrial ATP synthase. .

Gene Information

Human
Gene Name:	TMEM70
Uniprot:	Q9BUB7
Entrez:	54968

Gene Information

Family

Belongs to:

TMEM70 family

Family

Alternative Names

FLJ20533; transmembrane protein 70; transmembrane protein 70, mitochondrial

Molecular Weight

Mass (kDA):
28.969 kDA

Molecular Weight

Genomic Context


Human

Location:	8q21.11
Sequence:	8; NC_000008.11 (73976142..73982783)

Subcellular Localizations

Mitochondrion inner membrane; Multi-pass membrane protein.

Subcellular Localization

Diseases

Complex V Deficiency
Cardiomyopathies
Acidosis
3-@methylglutaconic Aciduria, Type I
Mitochondrial Diseases
Acidosis, Lactic
Hypertrophy
Hypertrophic Cardiomyopathy
Fetal Growth Retardation
Muscle Hypotonia
Hyperammonemia

Mitochondrial Encephalomyopathies
Inborn Errors Of Metabolism
Growth Retardation
Nicotinamide Adenine Dinucleotide Coenzyme Q Reductase Deficiency
Oligohydramnios
Malignant Neoplasm Of Breast

Disease

Pathways

Oxidative Phosphorylation
Excretion

Pathways

PTMs

Phosphorylation

Reduction

Bosterbio | ELISA Kits, Antibodies, Antibody Company

For details, visit:
bosterbio.com/bosterbio-gene-info-cards/TMEM70

References

PMID: 18953340 by Cizkova A., et al. TMEM70 mutations cause isolated ATP synthase deficiency and neonatal mitochondrial encephalocardiomyopathy.

PMID: 20937241 by Hejzlarova K., et al. Expression and processing of the TMEM70 protein.