Anti-MSRB3 Antibody

$99.00$319.00

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

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Rabbit Anti-MSRB3 Antibody (CSB-PA810290DSR1HU)

Supplier: CUSABIO BIOTECH CO.

Alternative names:

Methionine-R-sulfoxide reductase B3 Antibody,MsrB3 Antibody,MSRB3 Antibody,UNQ1965/PRO4487 Antibody

More alternative names for the antibody
Deafness, Autosomal Recessive 74 antibody|DFNB74 antibody|FLJ36866 antibody|Methionine R sulfoxide reductase B mitochondrial antibody|Methionine sulfoxide reductase B3 antibody|Methionine-R-sulfoxide reductase B3 antibody|MsrB3 antibody|MSRB3_HUMAN antibody
Anti-MSRB3 antibody [EPR13664] (ab180584)
Close sc-514897|

Recommended applications: ELISA, WB

Recommended dilution: User optimized

Recommended protocols: check protocols

Name

Anti-MSRB3 Antibody

Catalogue No.

CSB-PA810290DSR1HU

Reactivity

Human, Mouse

Immunogen

Recombinant human Methionine-R-sulfoxide reductase B3 protein (1-185AA)

Host

Rabbit

Applications

ELISA, WB

Recommended dilution

User optimized

Clonality

Polyclonal

Conjugation

unconjugated

Isotype

IgG

Molecular weight

20 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:253827( Human), Entrez Gene:320183( Mouse), Entrez Gene:680036( Rat), Omim:613719( Human), SwissProt:Q8IXL7( Human), SwissProt:Q8BU85( Mouse), Unigene:339024( Human)

Protein function

Catalyzes the reduction of free and protein-bound methionine sulfoxide to methionine. Isoform 2 is essential for hearing. .

Protein tissue specificity

Widely expressed. .

Involvement in disease

Deafness, autosomal recessive, 74 (DFNB74) [MIM:613718]: A form of non-syndromic sensorineural deafness characterized by prelingual, bilateral, profound hearing loss. Sensorineural deafness results from damage to the neural receptors of the inner ear, the nerve pathways to the brain, or the area of the brain that receives sound information. . Note=The disease is caused by mutations affecting the gene represented in this entry. A nonsense mutation affecting exclusively mitochondrial isoform 2 is sufficient to produce hearing loss.

Protein sequence and domain

Belongs to the MsrB Met sulfoxide reductase family.

Protein cellular localization

Isoform 1: Endoplasmic reticulum.; Isoform 2: Mitochondrion.

Research area

All research areas>Signaling Intermediates>MsrB
(View all antibody categories related to Signaling Intermediates)

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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