Sod1 Antibody

中文名稱：

Sod1兔多克隆抗體
貨號：

CSB-PA022397LA01MO
規格：

￥440
圖片：
Immunohistochemistry of paraffin-embedded human kidney tissue using CSB-PA022397LA01MO at dilution of 1:10

Immunoprecipitating Sod1 in HEK293 whole cell lysate
Lane 1: Rabbit control IgG instead of CSB-PA022397LA01MO in HEK293 whole cell lysate. For western blotting, a HRP-conjugated Protein G antibody was used as the secondary antibody (1/2000)
Lane 2: CSB-PA022397LA01MO (8µg) + HEK293 whole cell lysate (500µg)
Lane 3: HEK293 whole cell lysate (10µg)

Western Blot
Positive WB detected in: Hela whole cell lysate, 293T whole cell lysate, HepG2 whole cell lysate, Jurkat whole cell lysate, Rat brain tissue, Rat liver tissue, Mouse brain tissue
All lanes: Sod1 antibody at 3µg/ml
Secondary
Goat polyclonal to rabbit IgG at 1/50000 dilution
Predicted band size: 16 kDa
Observed band size: 16 kDa
其他：

產品詳情
產品評價
相關產品
靶點詳情

產品詳情

產品名稱：

Rabbit anti-Mus musculus (Mouse) Sod1 Polyclonal antibody
Uniprot No.：

P08228
基因名：

Sod1
別名：

Sod1 antibody; Superoxide dismutase [Cu-Zn] antibody; EC 1.15.1.1 antibody
宿主：

Rabbit
反應種屬：

Mouse, Rat, Human
免疫原：

Recombinant Mouse Superoxide dismutase [Cu-Zn] protein (2-154AA)
免疫原種屬：

Mus musculus (Mouse)

標記方式：

Non-conjugated

本頁面中的產品，Sod1 Antibody (CSB-PA022397LA01MO)，的標記方式是Non-conjugated。對于Sod1 Antibody，我們還提供其他標記。見下表：

標記方式	貨號	產品名稱	應用
HRP	CSB-PA022397LB01MO	Sod1 Antibody, HRP conjugated	ELISA
FITC	CSB-PA022397LC01MO	Sod1 Antibody, FITC conjugated
Biotin	CSB-PA022397LD01MO	Sod1 Antibody, Biotin conjugated	ELISA

克隆類型：

Polyclonal
抗體亞型：

IgG
純化方式：

>95%, Protein G purified
濃度：

It differs from different batches. Please contact us to confirm it.
保存緩沖液：

Preservative: 0.03% Proclin 300
Constituents: 50% Glycerol, 0.01M PBS, PH 7.4
產品提供形式：

Liquid
應用范圍：

ELISA, WB, IHC, IP

推薦稀釋比：

Application	Recommended Dilution
WB	1:500-1:5000
IHC	1:10-1:100
IP	1:200-1:2000

Protocols：

ELISA Protocol
Western Blotting (WB) Protocol
Immunohistochemistry (IHC) Protocol
Immunoprecipitation (IP) Protocol
儲存條件：

Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
貨期：

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.
用途：

For Research Use Only. Not for use in diagnostic or therapeutic procedures.

產品評價

靶點詳情

功能：

Destroys radicals which are normally produced within the cells and which are toxic to biological systems.
基因功能參考文獻：
1. These findings suggest unexpected specificity, mediated by both the primary protein pathology and cellular context, in the induced "secondary aggregation" of a mutant form of SOD1 that could be viewed as a reporter of proteostatic function PMID: 29776378
2. Presence of mutated SOD1 protein affects the MHC class I molecules expression and is associated with facial injured motoneurons. PMID: 29943955
3. DKO mice spontaneously develop severe liver failure at a relatively young stage, they have the potential for use as a model for hepatic disorders and for testing other potential treatments. PMID: 30050648
4. These results suggest that overexpression of SQSTM1 in SOD1 (H46R) mice accelerates disease onset by compromising the protein degradation pathways. PMID: 29843805
5. Results support the concept that impaired redox signaling, rather than oxidative damage, in peripheral nerve plays a key role in muscle loss in Sod1(-/-) mice and potentially sarcopenia during aging PMID: 29065712
6. This evidence favours mutant SOD1-containing astrocytes releasing destructive species that alter the biology of adjacent astrocytes PMID: 28861673
7. Given the close association of stress granules and TDP-43, we wondered whether internalisation of SOD1 aggregates stimulated TDP-43 cytosolic aggregate structures. Addition of recombinant mutant G93A SOD1 aggregates to NSC-34 cells was found to trigger a rapid shift of TDP-43 to the cytoplasm where it was still accumulated after 48 h. PMID: 28560609
8. Distinct roles for motor neuron autophagy early and late in the SOD1(G93A) mouse model of ALS. PMID: 28904095
9. It was observed that global AQP4 expression increased in the spinal cord of SOD1G93A mice as the disease progressed. However, AQP4 polarization decreased as the disease progressed, and AQP4 polarized localization at the endfeet of astrocytes was decreased in the spinal ventral horn of SOD1G93A mice at the disease onset and end stages. PMID: 28627708
10. Superoxide dismutase 1 mutation is associated with amyotrophic lateral sclerosis. PMID: 28019127
11. Restrictive Lung Disease in the Cu/Zn Superoxide-Dismutase 1 G93A Amyotrophic Lateral Sclerosis Mouse Model. PMID: 28248134
12. Endogenous MIF reduces the accumulation and toxicity of misfolded SOD1 in a mouse model of amyotrophic lateral sclerosis. PMID: 27551074
13. This study indicates that axonal and neuromuscular junction degeneration in the SOD1 model of amyotrophic lateral sclerosis is a complex and evolving sequence of events PMID: 27038603
14. In this newborn mouse lung hypoxia-reoxygenation model, we found downregulation of genes of mediators of inflammation, an antiapoptotic gene expression pattern, and downregulation of DNA glycosylases. Sod1 and Il1b were significantly differentially expressed when comparing reoxygenation using 60% O2 with air. PMID: 27529351
15. the senescence associated secretory phenotype was also increased significantly in the kidney of Sod1(-/)(-) mice compared to WT mice as measured by the expression of transcripts for IL-6 and IL-1b PMID: 27846439
16. Our study provides the first direct evidence that Abeta, an AD-linked factor, is associated to the pathogenesis of ALS and provides molecular clues to understand common aggregation mechanisms in the pathogenesis of neurodegenerative diseases. PMID: 28864422
17. deletion-rescue experiments show that a respiration-defective mutant of SOD1 is also impaired in its ability to rescue cells from toxicity caused by SOD1 deletion PMID: 28739857
18. These findings indicate that a loss of Sig1R function is causative for juvenile amyotrophic lateral sclerosis (ALS16), and collapse of the mitochondria-associated membrane is a common pathomechanism in both Sig1R- and SOD1-linked ALS. PMID: 27821430
19. the aberrant mutant SOD1-G3BP1 interaction affects stress granule dynamics PMID: 27481264
20. the absence of IP3R2 led to increased innate immunity, which may contribute to the decreased survival of the SOD1(G93A) mice.our data indicate that IP3R2 protects against the negative effects of inflammation, suggesting that the increase in IP3R2 expression in ALS patients is a protective response. PMID: 27378687
21. the redox regulation of Jmjd3 is a unique regulatory mechanism for Cu,Zn-superoxide dismutase-mediated profibrotic macrophage polarization. PMID: 26699812
22. two ALS-linked factors, SQSTM1 and ALS2, have distinct but additive protective roles against mutant SOD1-mediated toxicity by modulating neuronal proteostasis possibly through the autophagy-endolysosomal system. PMID: 27439389
23. we showed that, in the absence of ERalpha, G93A-SOD1 failed to activate OMI and the proteasome, confirming the ERalpha dependence of the response. Taken together, these results demonstrate the IMS-UPRmt activation in SOD1 familial Amyotrophic lateral sclerosis , and suggest that sex differences in the disease phenotype could be linked to differential activation of the ERa axis of the IMS-UPRmt PMID: 28186560
24. The cross-sectional area of the pial arteriolar wall was increased in SOD1 deficiency, and a hyperhomocysteinemic diet sensitized SOD1-deficient mice to this hypertrophic effect. Analysis of of the vascular wall demonstrated a increase in the content of smooth muscle and elastin. We conclude that superoxide is a driver of both cerebral vascular hypertrophy and vasomotor dysfunction in a model of hyperhomocysteinemia. PMID: 28414812
25. SOD1 has a role in amyotrophic lateral sclerosis disease phenotype PMID: 26878886
26. the damage and satellite cell state of the gastrocnemius muscle in SOD1 knockout mice, was investigated. PMID: 26798428
27. Events occurring locally in the skeletal muscle of SOD1 mutant mice contribute to the impairment of CaV1.1 function in ALS muscle independently of innervation status. PMID: 27340545
28. G85R-SOD1:YFP inclusion pathology quickly spreads to discrete neurons in the brainstem and midbrain that are synaptically connected to spinal neurons PMID: 26650262
29. SOD1 aggregates interact with the cell surface triggering activation of Rac1 and subsequent membrane ruffling permitting aggregate uptake via stimulated macropinocytosis PMID: 26520394
30. age-related increases were mitigated by caloric restriction but not super oxide dismutase 1 overexpression PMID: 26476235
31. postmitotic expression SOD1G93A mutant gene promotes a FAPS phenotype in C2C12 cells, by upregulating HDAC4 protein and preventing the BAF60C-SWI/SNF complex myogenic commitment PMID: 26491230
32. The oxidative stress of diabetes mellitus impairs Wnt signaling and causes cardiac outlet defects that are rescued by SOD1 overexpression PMID: 26232087
33. This study demonistrated that proprioceptive nerve endings in muscles revealed early and significant alterations at Ia/II proprioceptive nerve endings in muscle spindles and occur alongside those at alpha-motor axons in SOD1(G93A) mice. PMID: 26136049
34. Mutant SOD1 Increases APP Expression and Phosphorylation in Cellular and Animal Models of ALS PMID: 26600047
35. despite the low visceral fat in Sod1-knockout (KO) mouse, lipid droplets accumulate in the liver to a greater extent than for the wild-type mouse upon fasting PMID: 26474701
36. Loss of SOD1 recapitulates many neuromuscular and muscle fiber changes seen in old mice. PMID: 25841780
37. mutation is a cause of amyotrophic lateral sclerosis. PMID: 25736480
38. Cys111 is a critical residue for the neuronal toxicity of mutant SOD1 in vivo, and the blockage of peroxidation of this residue in mutant SOD1 may constitute a future target for developing ALS treatment. PMID: 25762155
39. Homozgous Sod1(D83G/D83G) mutant mice develop progressive degeneration of lower and upper motor neurons. PMID: 25468678
40. Although the protein levels of the three catalytic components of the proteasome, beta1, beta2, and beta5, were not significantly altered, their proteolytic activities were decreased in the SOD1-deficient RBCs PMID: 26264915
41. SOD1 aggregation follows robust and simplistic rules, providing new mechanistic insights into the amyotrophic lateral sclerosis pathology. PMID: 26221023
42. elevation in hyperoxidized Prxs, notably Prx2 and Prx3, was observed in several organs from SOD1-deficient mice. However, a SOD1 deficiency had no impact on the wheel-running activity of the mice PMID: 26079888
43. young adult Sod1-/- mice display reduction in skeletal muscle mass and gross alterations in neuromuscular junction. PMID: 24971750
44. Phenotype of transgenic mice carrying a very low copy number of the mutant human G93A SOD-1 gene is associated with amyotrophic lateral sclerosis. PMID: 24945277
45. SOD prevents thrombomodulin methionine oxidation, promotes protein C activation, and protects against arterial and venous thrombosis in mice. PMID: 26069236
46. Studied whether NO exerts modulation of superoxide levels throughout the arterial wall and if it regulates NO-dependent inhibition of neointimal hyperplasia. In vivo, NO increased SOD-1 levels following carotid artery balloon injury in a rat model. PMID: 25460325
47. Lipogenesis is activated by oxidative stress, which is more prominent in the case of Sod1 deficiency, and appears to participate in liver steatosis. PMID: 26116535
48. in a SOD1(G93A) mouse model of amyotrophic lateral sclerosis, resveratrol ameliorates motor neuron degeneration PMID: 25057490
49. exposure to either 14- or 28-day chronic stress resulted in a depressive-like syndrome, behavioural invigoration and aggression, and decreased activity of two major brain peroxidation enzymes, superoxide dismutase and catalase. PMID: 24786329
50. Study examined the ease with which motor neuron disease can be transmitted by injecting spinal cord homogenates prepared from paralyzed mice expressing mutant superoxide dismutase 1 into the spinal cords of genetically vulnerable SOD1 transgenic mice PMID: 25262000
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亞細胞定位：

Cytoplasm. Nucleus.
蛋白家族：

Cu-Zn superoxide dismutase family
數據庫鏈接：

KEGG: mmu:20655

STRING: 10090.ENSMUSP00000023707

UniGene: Mm.276325

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