Anti-MOCS1 Antibody

$99.00$319.00

Reactivity: Human,Mouse
Applications: ELISA,WB
Conjugation: Various
Supplier: CUSABIO BIOTECH CO.

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Rabbit Anti-MOCS1 Antibody (CSB-PA878934ESR1HU)

Supplier: CUSABIO BIOTECH CO.

Alternative names:

Molybdenum cofactor biosynthesis protein 1 Antibody,Cell migration-inducing gene 11 protein Antibody,Molybdenum cofactor synthesis-step 1 protein A-B Antibody,Cyclic pyranopterin monophosphate synthase Antibody,Molybdenum cofactor biosynthesis protein A Antibody,Cyclic pyranopterin monophosphate synthase accessory protein Antibody,Molybdenum cofactor biosynthesis protein C Antibody,MOCS1 Antibody,MIG11 Antibody

More alternative names for the antibody
Cell migration-inducing gene 11 protein antibody|MIG11 antibody|MOCOD antibody|Mocs1 antibody|MOCS1_HUMAN antibody|Molybdenum cofactor biosynthesis protein 1 antibody|Molybdenum cofactor biosynthesis protein A antibody|Molybdenum cofactor biosynthesis protein C antibody|Molybdenum cofactor synthesis 1 antibody|Molybdenum cofactor synthesis-step 1 protein A-B antibody
Anti-MOCS1 antibody (ab126560)
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Recommended applications: ELISA, WB

Recommended dilution: User optimized

Recommended protocols: check protocols

Name

Anti-MOCS1 Antibody

Catalogue No.

CSB-PA878934ESR1HU

Reactivity

Human, Mouse

Immunogen

Recombinant human Molybdenum cofactor biosynthesis protein 1 protein (90-360AA)

Host

Rabbit

Applications

ELISA, WB

Recommended dilution

User optimized

Clonality

Polyclonal

Conjugation

unconjugated

Isotype

IgG

Molecular weight

70 kDa

Purification

Antigen Affinity Purified

Storage

Shipped at 4 Celcius Degree. Upon delivery aliquot and store at -20 Celcius Degree or -80 Celcius Degree. Avoid repeated freeze.

Database links

Entrez Gene:4337( Human), Omim:603707( Human), SwissProt:Q9NZB8( Human), Unigene:718492( Human)

Protein function

Isoform MOCS1A and isoform MOCS1B probably form a complex that catalyzes the conversion of 5′-GTP to cyclic pyranopterin monophosphate (cPMP). MOCS1A catalyzes the cyclization of GTP to (8S)-3′,8-cyclo-7,8-dihydroguanosine 5′-triphosphate and MOCS1B catalyzes the subsequent conversion of (8S)-3′,8-cyclo-7,8-dihydroguanosine 5′-triphosphate to cPMP. .

Protein tissue specificity

Isoform MOCS1A and isoform 2 are widely expressed. .

Involvement in disease

Molybdenum cofactor deficiency, complementation group A (MOCODA) [MIM:252150]: An autosomal recessive metabolic disorder leading to the pleiotropic loss of molybdoenzyme activities. It is clinically characterized by onset in infancy of poor feeding, intractable seizures, severe psychomotor retardation, and death in early childhood in most patients. . Note=The disease is caused by mutations affecting the gene represented in this entry.

Protein sequence and domain

In the C-terminal section; belongs to the MoaC family.; In the N-terminal section; belongs to the radical SAM superfamily. MoaA family.

Research area

All research areas>Synthesis and Degradation>MOCS
(View all antibody categories related to Synthesis and Degradation)

Note

AntibodyPlus provides antibody trial sample for your own antibody validation and collects antibody reviews.

Supplier

CUSABIO BIOTECH CO.

Product type

Primary antibody

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