SARDH Antibodies

AND SARDH ELISA kits, SARDH Proteins

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

We validate the specificity of these antibodies to SARDH by testing them on tissues known to express SARDH positively and negatively. Browse below to find the SARDH antibody that suites your experiment. We have 2 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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SARDH Infographic by Boster Bio

All SARDH Products

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SARDH (NM_007101) Human Over-expression Lysate

Human

$960
Cat # LS001757
20 µg, 100 µg

Anti-SARDH Antibody Picoband®

Western blot analysis of SARDH using anti-SARDH antibody (A09641-1)

Flow Cytometry analysis of U87 cells using anti-SARDH antibody (A09641-1)

Human, Mouse, Rat

ELISA, Flow Cytometry, WB

$370
Cat # A09641-1
100 μg/vial

SARDH Overview

Facts about Sarcosine dehydrogenase, mitochondrial.

SARDH 3D structure. Source: alphafold

Sarcosine dehydrogenase, mitochondrial (SARDH)

Gene Information

Human
Gene Name:	SARDH
Uniprot:	Q9UL12
Entrez:	1757

Family

Belongs to:

GcvT family

Alternative Names

BPR-2; dimethylglycine dehydrogenase-like 1; DMGDHL1; FLJ36475; mitochondrial; SAR; sarcosine dehydrogenase; SARD; SDH

Molecular Weight

Mass (kDA):
101.037 kDA

Genomic Context


Human

Location:	9q34.2
Sequence:	9; NC_000009.12 (133663074..133739958, complement)

Subcellular Localizations

Mitochondrion matrix.

Diseases

Sarcosinaemia
Myocarditis
Cardiomyopathy, Dilated
Cardiomyopathies
Heart Diseases
Mitochondrial Diseases
Carcinoma
Cardiovascular Diseases
Malignant Neoplasms
Neoplasms
Nervousness
5,10-methylenetetrahydrofolate Reductase Deficiency

Riboflavin Deficiency
Amino Acid Metabolism, Inborn Errors
Cell Invasion
Malignant Neoplasm Of Prostate
Hereditary Diseases
Congenital Abnormality

Pathways

Oxidative Demethylation
Localization
Demethylation
Methylation
Cell Proliferation
Dna Methylation

Pathogenesis

PTMs

Demethylation
Nitrosylation

Reduction
Glycosylation

Methylation

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

References

PMID: 10444331 by Eschenbrenner M., et al. Cloning and mapping of the cDNA for human sarcosine dehydrogenase, a flavoenzyme defective in patients with sarcosinemia.

PMID: 10686491 by Gilbert J.R., et al. Physical and cDNA mapping in the DBH region of human chromosome 9q34.