SELENON Antibody

Code CSB-PA878943LA01HU
Size US$166
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  • Western Blot
    Positive WB detected in: Rat brain tissue, Rat lung tissue
    All lanes: SELENON antibody at 4.2μg/ml
    Secondary
    Goat polyclonal to rabbit IgG at 1/50000 dilution
    Predicted band size: 66, 63 kDa
    Observed band size: 66 kDa

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Product Details

Full Product Name
Rabbit anti-Homo sapiens (Human) SELENON Polyclonal antibody
Uniprot No.
Target Names
SELENON
Alternative Names
CFTD antibody; MDRS1 antibody; RSMD1 antibody; RSS antibody; Selenoprotein N antibody; Selenoprotein N, 1 antibody; SelN antibody; SELN_HUMAN antibody; sepn1 antibody
Raised in
Rabbit
Species Reactivity
Human, Rat
Immunogen
Recombinant Human Selenoprotein N protein (135-219AA)
Immunogen Species
Homo sapiens (Human)
Conjugate
Non-conjugated

The SELENON Antibody (Product code: CSB-PA878943LA01HU) is Non-conjugated. For SELENON Antibody with conjugates, please check the following table.

Available Conjugates
Conjugate Product Code Product Name Application
HRP CSB-PA878943LB01HU SELENON Antibody, HRP conjugated ELISA
FITC CSB-PA878943LC01HU SELENON Antibody, FITC conjugated
Biotin CSB-PA878943LD01HU SELENON Antibody, Biotin conjugated ELISA
Clonality
Polyclonal
Isotype
IgG
Purification Method
>95%, Protein G purified
Concentration
It differs from different batches. Please contact us to confirm it.
Buffer
Preservative: 0.03% Proclin 300
Constituents: 50% Glycerol, 0.01M PBS, pH 7.4
Form
Liquid
Tested Applications
ELISA, WB
Recommended Dilution
Application Recommended Dilution
WB 1:500-1:5000
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
Plays an important role in cell protection against oxidative stress and in the regulation of redox-related calcium homeostasis. Regulates the calcium level of the ER by protecting the calcium pump ATP2A2 against the oxidoreductase ERO1A-mediated oxidative damage. Within the ER, ERO1A activity increases the concentration of H(2)O(2), which attacks the luminal thiols in ATP2A2 and thus leads to cysteinyl sulfenic acid formation (-SOH) and SEPN1 reduces the SOH back to free thiol (-SH), thus restoring ATP2A2 activity. Acts as a modulator of ryanodine receptor (RyR) activity: protects RyR from oxidation due to increased oxidative stress, or directly controls the RyR redox state, regulating the RyR-mediated calcium mobilization required for normal muscle development and differentiation.; Essential for muscle regeneration and satellite cell maintenance in skeletal muscle.
Gene References into Functions
  1. Case Report: rigid spine muscular dystrophy 1 in a compound heterozygote with two novel mutations in SEPN1 gene; a novel missense mutation (c.1384T>C; p.Sec462Arg) and a novel nonsense mutation (c.1525C>T; p.Gln509Ter), inherited from his father and mother respectively. PMID: 27863379
  2. We report two previously undescribed mutations in SEPN1. Our study adds two novel homozygous mutations to the number of reported pathogenic SEPN1 variants. PMID: 26780752
  3. The physiological function of SelN in muscle tissue and the pathogenesis leading to SEPN1-related myopathies. [Review] PMID: 22527882
  4. Data show that the spectrum of severity of SEPN1-related myopathiesis wider than previously reported. PMID: 21670436
  5. Data show that Argonaute 2 expression is critical for stem cells to escape senescence by downregulating miR10b and miR23b, and that selenoprotein N1 is also involved in ATSC survival and self-renewal through ROS-mediated p38 MAPK inactivation. PMID: 21241449
  6. this series of patients illustrates the clinical, histopathological and MRI findings of SEPN1-related myopathy. It also adds new mutations to the limited number of fully described pathogenic SEPN1 variants. PMID: 20937510
  7. Mutations of the selenoprotein N gene, which is implicated in rigid spine muscular dystrophy, cause the classical phenotype of multiminicore disease PMID: 12192640
  8. A new SEPN1 point mutation, 943g->A causing G315S was found in a rigid spine muscular dystrophy patient with cor pulmonale. PMID: 15668457
  9. SEPN1 mutation analysis revealed that the patient was a compound heterozygote: a previously described insertion (713-714 insA), and a novel nonsense mutation (R439stop). PMID: 15792869
  10. Two patients with 'Dropped head syndrome' due to mutations in SEPN1 genes. PMID: 15961312
  11. SEPN1 is the second genetic cause of CFTD and the first cause of autosomal recessive CFTD to be identified to our knowledge. CFTD is the fourth clinicopathological presentation that can be associated with mutations in SEPN1. PMID: 16365872
  12. identification of this mutation affecting a conserved base in the selenocysteine insertion sequence functional motif thereby reveals the structural basis for a novel pathological mechanism leading to SEPN1-related myopathy PMID: 16498447
  13. We report on the possible molecular mechanism behind these mutations in SEPN1. Our study clarifies molecular mechanisms of this muscular disorder. PMID: 16779558
  14. SEPN1 and RYR1 are required for the same cellular differentiation events and are needed for normal calcium fluxes PMID: 18713863
  15. Data highlights the importance of the SRE element during SelN expression and illustrates a novel molecular mechanism by which point mutations may lead to SEPN1-related myopathy. PMID: 19067361
  16. SelN plays a key role in redox homeostasis and human cell protection against oxidative stress. PMID: 19557870
  17. The Alu-derived exon 3 of human SEPN1 acquired its muscle-specific splicing activity after the divergence of humans and chimpanzees, suggesting its potential role in human evolution. PMID: 18841251

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Involvement in disease
Rigid spine muscular dystrophy 1 (RSMD1); Myopathy, congenital, with fiber-type disproportion (CFTD)
Subcellular Location
[Isoform 2]: Endoplasmic reticulum membrane.
Tissue Specificity
Isoform 1 and isoform 2 are expressed in skeletal muscle, brain, lung and placenta. Isoform 2 is also expressed in heart, diaphragm and stomach.
Database Links

HGNC: 15999

OMIM: 255310

KEGG: hsa:57190

STRING: 9606.ENSP00000355141

UniGene: Hs.323396

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