TGDS Antibodies

AND TGDS ELISA kits, TGDS Proteins

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

We validate the specificity of these antibodies to TGDS by testing them on tissues known to express TGDS positively and negatively. Browse below to find the TGDS antibody that suites your experiment. We have 1 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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TGDS Infographic by Boster Bio

All TGDS Products

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TGDS (NM_014305) Human Over-expression Lysate

Human

$628
Cat # LS023483
20 µg, 100 µg

TGDS Overview

Facts about dTDP-D-glucose 4,6-dehydratase.

TGDS 3D structure. Source: alphafold

dTDP-D-glucose 4,6-dehydratase (TGDS)

Gene Information

Human
Gene Name:	TGDS
Uniprot:	O95455
Entrez:	23483

Family

Belongs to:

NAD(P)-dependent epimerase/dehydratase family

Alternative Names

dTDP-D-glucose 4,6-dehydratase; EC 4.2.1.46; growth-inhibiting protein 21; P; SDR2E1; short chain dehydrogenase/reductase family 2E, member 1; TDPGD; TDP-glucose 4,6-dehydratase

Molecular Weight

Mass (kDA):
40.214 kDA

Genomic Context


Human

Location:	13q32.1
Sequence:	13; NC_000013.11 (94574054..94596274, complement)

Diseases

Depressive Disorder
Cognition Disorders
Diabetes Mellitus
Diabetes Mellitus, Non-insulin-dependent
Hypertensive Disease
Impaired Cognition
Partial Seizure
Dementia
Coronary Artery Disease
Exanthema
Cerebrovascular Accident

Hyperlipidemia
Mild Cognitive Disorder
Depressive Symptom
Graft-vs-host Disease
Complications Of Diabetes Mellitus

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

References

PMID: 25480037 by Ehmke N., et al. Homozygous and compound-heterozygous mutations in TGDS cause Catel- Manzke syndrome.