Catalog No.
YHB84401
Expression system
E. coli
Species
Homo sapiens (Human)
Protein length
Val2-Gly88
Predicted molecular weight
37.81 kDa
Nature
Recombinant
Endotoxin level
Please contact with the lab for this information.
Purity
>90% as determined by SDS-PAGE.
Accession
O96033
Applications
ELISA, Immunogen, SDS-PAGE, WB, Bioactivity testing in progress
Form
Lyophilized
Storage buffer
Lyophilized from a solution in PBS pH 7.4, 0.02% NLS, 1mM EDTA, 4% Trehalose, 1% Mannitol.
Reconstitution
Reconstitute in sterile water for a stock solution. A copy of datasheet will be provided with the products, please refer to it for details.
Shipping
In general, proteins are provided as lyophilized powder/frozen liquid. They are shipped out with dry ice/blue ice unless customers require otherwise.
Stability and Storage
Use a manual defrost freezer and avoid repeated freeze thaw cycles. Store at 2 to 8°C for frequent use. Store at -20 to -80°C for twelve months from the date of receipt.
Alternative Names
Molybdopterin synthase sulfur carrier subunit, MOCO1-A, Molybdenum cofactor synthesis protein 2 small subunit, Molybdenum cofactor synthesis protein 2A, MOCS2A, Molybdopterin-synthase small subunit, Sulfur carrier protein MOCS2A, MOCS2, MOCO1
Novel pathogenic variant in a mild case of type B molybdenum cofactor deficiency: case report and literature review., PMID:39695700
Exome Sequencing of Consanguineous Pashtun Families With Familial Epilepsy Reveals Causative and Candidate Variants in TSEN54, MOCS2, and OPHN1., PMID:39400946
Examining the liver-pancreas crosstalk reveals a role for the molybdenum cofactor in β-cell regeneration., PMID:39159974
Downstream Target Analysis for miR-365 among Oral Squamous Cell Carcinomas Reveals Differential Associations with Chemoresistance., PMID:38929724
On pathways and blind alleys-The importance of biomarkers in vitamin B6 -dependent epilepsies., PMID:37428623
Live Birth of a Healthy Child in a Couple with Identical mtDNA Carrying a Pathogenic c.471_477delTTTAAAAinsG Variant in the MOCS2 Gene., PMID:36980992
Molybdenum Cofactor Deficiency in Humans., PMID:36296488
Beyond Moco Biosynthesis-Moonlighting Roles of MoaE and MOCS2., PMID:35744859
Proteins Structure Models in the Evaluation of Novel Variant (C.472_477del) in the MOCS2 Gene., PMID:33066491
ETHE1 and MOCS1 deficiencies: Disruption of mitochondrial bioenergetics, dynamics, redox homeostasis and endoplasmic reticulum-mitochondria crosstalk in patient fibroblasts., PMID:31477743
Mild phenotype in Molybdenum cofactor deficiency: A new patient and review of the literature., PMID:30900395
Genome-wide identification of genes essential for podocyte cytoskeletons based on single-cell RNA sequencing., PMID:28709640
Molybdenum cofactor deficiency: Identification of a patient with homozygote mutation in the MOCS3 gene., PMID:28544736
Molybdenum cofactor and isolated sulphite oxidase deficiencies: Clinical and molecular spectrum among Egyptian patients., PMID:27289259
Mouse model for molybdenum cofactor deficiency type B recapitulates the phenotype observed in molybdenum cofactor deficient patients., PMID:27138983
Molybdenum cofactor deficiency causes translucent integument, male-biased lethality, and flaccid paralysis in the silkworm Bombyx mori., PMID:27041280
[Coexpression of genes located in the 111.35-116.16 Mb of chromosome 13 in mice with different predisposition to catalepsy]., PMID:25842858
Investigation of molybdenum cofactor deficiency due to MOCS2 deficiency in a newborn baby., PMID:25709896
Pyridoxine-dependent epilepsy with elevated urinary α-amino adipic semialdehyde in molybdenum cofactor deficiency., PMID:23147983
Molybdenum cofactor deficiency: review of 12 cases (MoCD and review)., PMID:23122324
Genomic aberrations in lung adenocarcinoma in never smokers., PMID:21151896
Molybdenum cofactor deficiency: Mutations in GPHN, MOCS1, and MOCS2., PMID:21031595
Maternal uniparental isodisomy is responsible for serious molybdenum cofactor deficiency., PMID:20573177
Functional deficiencies of sulfite oxidase: Differential diagnoses in neonates presenting with intractable seizures and cystic encephalomalacia., PMID:19793632
Molybdenum cofactor deficiency: clinical features in a Turkish patient., PMID:17158010
A Turkish case with molybdenum cofactor deficiency., PMID:17065069
A novel MOCS2 mutation reveals coordinated expression of the small and large subunit of molybdopterin synthase., PMID:16737835
Ten novel mutations in the molybdenum cofactor genes MOCS1 and MOCS2 and in vitro characterization of a MOCS2 mutation that abolishes the binding ability of molybdopterin synthase., PMID:16021469
Mutations in the molybdenum cofactor biosynthetic genes MOCS1, MOCS2, and GEPH., PMID:12754701
Prenatal diagnosis of molybdenum cofactor deficiency and isolated sulfite oxidase deficiency., PMID:12533804
Functionality of alternative splice forms of the first enzymes involved in human molybdenum cofactor biosynthesis., PMID:11891227
A mutation in the gene for the neurotransmitter receptor-clustering protein gephyrin causes a novel form of molybdenum cofactor deficiency., PMID:11095995
Genetics of molybdenum cofactor deficiency., PMID:10746556
Human molybdopterin synthase gene: genomic structure and mutations in molybdenum cofactor deficiency type B., PMID:10053004
For research use only. Not for human or drug use.
