MSRB3 Antibody

Code CSB-PA810290DSR1HU
Size US$166
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  • Western blot
    All lanes: MSRB3 antibody at 4.61 μg/ml
    Lane 1: Mouse large intestine tissue
    Lane 2: Mouse lung tissue
    Lane 3: Mouse gonadal tissue
    Lane 4: Mouse heart tissue
    Secondary
    Goat polyclonal to rabbit IgG at 1/10000 dilution
    Predicted band size: 21 kDa
    Observed band size: 21 kDa

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Product Details

Full Product Name
Rabbit anti-Homo sapiens (Human) MSRB3 Polyclonal antibody
Uniprot No.
Target Names
MSRB3
Alternative Names
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
Raised in
Rabbit
Species Reactivity
Human, Mouse
Immunogen
Recombinant Human Methionine-R-sulfoxide reductase B3 protein (1-185AA)
Immunogen Species
Homo sapiens (Human)
Conjugate
Non-conjugated
Clonality
Polyclonal
Isotype
IgG
Purification Method
Antigen Affinity Purified
Concentration
It differs from different batches. Please contact us to confirm it.
Buffer
PBS with 0.02% sodium azide, 50% glycerol, pH7.3.
Form
Liquid
Tested Applications
ELISA, WB
Recommended Dilution
Application Recommended Dilution
WB 1:1000-1:5000
Troubleshooting and FAQs
Storage
Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
Lead Time
Basically, we can dispatch the products out in 1-3 working days after receiving your orders. Delivery time maybe differs from different purchasing way or location, please kindly consult your local distributors for specific delivery time.

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Target Background

Function
Catalyzes the reduction of free and protein-bound methionine sulfoxide to methionine. Isoform 2 is essential for hearing.
Gene References into Functions
  1. we characterise the mammalian enzyme Msr B3. There are two splice variants of this enzyme that differ only in their N-terminal signal sequence, which directs the protein to either the endoplasmic reticulum (ER) or mitochondria PMID: 29420254
  2. This characterization of GWAS-implicated MSRB3 protein expression in human hippocampus suggests that patterns of neuronal and vascular MsrB3 protein expression reflect or underlie pathology associated with Alzheimer disease. PMID: 28777754
  3. Oncogene induction in differentiated cells induces massive DNA damage, mammary stem cells are resistant, owing to a preemptive program driven by ZEB1 and MSRB3. The prevention of oncogene-induced DNA damage precludes induction of the oncosuppressive p53-dependent DNA-damage response, thereby increasing stem cells' intrinsic susceptibility to malignant transformation. PMID: 28394329
  4. The data suggest that MsrB3 attenuates HO-1 induction by inhibiting reactive oxygen species production, endoplasmic reticulum stress, and Nrf2 activation. PMID: 27059143
  5. MsrB3 plays an important role in cancer cell survival through the modulation of the intrinsic apoptosis pathway. PMID: 28007593
  6. Taken together, our results suggest that MsrB3 plays a critical role in cancer cell apoptosis through the modulation of ER stress status. PMID: 28389299
  7. MsrB3 deficiency activates the cell cycle inhibitors p21 and p27. PMID: 24583268
  8. DNA methylation shows genome-wide association of NFIX, RAPGEF2 and MSRB3 with gestational age at birth. PMID: 22422452
  9. these data provide evidence that the ER-type of MsrB3 plays an important role in protection against ER stress, suggesting that MsrB3 may be involved in the regulation of ER homeostasis. PMID: 22405767
  10. Taken together, these data provide evidence that the ER type of MsrB, MsrB3A, plays an important role in protection mechanisms against oxidative, cold and heat stresses and, moreover, in the regulation of fruit fly aging. PMID: 22310715
  11. Results identified an antimicrobial peptide from the human methionine sulfoxide reductase B3 protein. PMID: 22027001
  12. an in vitro assay revealed that p.Cys89Gly completely abolished MSRB3 enzymatic activity and that p.Arg19X is a null allele for MSRB3 mitochondrial isoforms, indicating that DFNB74 deafness might be a mitochondrial disease limited to the inner ear. PMID: 21185009
  13. Observational study and genome-wide association study of gene-disease association. (HuGE Navigator) PMID: 20195514

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Involvement in disease
Deafness, autosomal recessive, 74 (DFNB74)
Subcellular Location
[Isoform 1]: Endoplasmic reticulum.; [Isoform 2]: Mitochondrion.
Protein Families
MsrB Met sulfoxide reductase family
Tissue Specificity
Widely expressed.
Database Links

HGNC: 27375

OMIM: 613718

KEGG: hsa:253827

STRING: 9606.ENSP00000347324

UniGene: Hs.339024

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