MSMO1 Antibodies

AND MSMO1 ELISA kits, MSMO1 Proteins

Many biological assays use antibodies to detect MSMO1, such as Western Blot (WB), ELISA, Flow Cytometry, Immunocytochemistry (IHC). These antibodies can be polyclonal or monoclonal, and react with MSMO1 in Human, Mouse, Rat, and many other animal samples. Boster Bio use mainly mouse and rabbit to develop MSMO1 antibodies...

We validate the specificity of these antibodies to MSMO1 by testing them on tissues known to express MSMO1 positively and negatively. Browse below to find the MSMO1 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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MSMO1 Infographic by Boster Bio

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C 4 Methylsterol Oxidase (MSMO1) (NM_001017369) Human Over-expression Lysate

Human

$628
Cat # LS006307
20 µg, 100 µg

MSMO1 Overview

Facts about Methylsterol monooxygenase 1.

MSMO1 3D structure. Source: alphafold

Methylsterol monooxygenase 1 (MSMO1)

Catalyzes the first step in the elimination of the two C-4 methyl groups of 4,4-dimethylzymosterol. .

Gene Information

Human
Gene Name:	MSMO1
Uniprot:	Q15800
Entrez:	6307

Family

Belongs to:

sterol desaturase family

Alternative Names

C-4 methyl sterol; C-4 methylsterol oxidase; EC 1.14.13.72; ERG25DESP4Methylsterol monooxygenase; MGC104344; sterol-C4-methyl oxidase-like

Molecular Weight

Mass (kDA):
35.216 kDA

Genomic Context


Human

Location:	4q32.3
Sequence:	4; NC_000004.12 (165327666..165343164)

Subcellular Localizations

Endoplasmic reticulum membrane; Multi-pass membrane protein.

Diseases

Microcephaly, congenital cataract, and psoriasiform dermatitis (MCCPD)

For details, visit:
bosterbio.com/bosterbio-gene-info-cards/MSMO1

References

PMID: 8663358 by Li L., et al. Characterization of yeast methyl sterol oxidase (ERG25) and identification of a human homologue.

PMID: 21285510 by He M., et al. Mutations in the human SC4MOL gene encoding a methyl sterol oxidase cause psoriasiform dermatitis, microcephaly, and developmental delay.