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NOX2 (PT0125R) PT® Rabbit mAb

-YM8068

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Catalog: YM8068
Size
Price
Status
Qty.
200μL
$600.00
In stock

0

100μL
$340.00
In stock

0

40μL
$190.00
In stock

0

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Main Information
Target

gp91-phox

Host Species

Rabbit

Reactivity

Human, Mouse, Rat,

Applications

WB, IP, ELISA

MW

65kD (Calculated)

65kD (Observed)

Conjugate/Modification


Unmodified

Detailed Information
Recommended Dilution Ratio
WB 1:1000-5000; ELISA 1:5000-20000; IP 1:50-200
Formulation
PBS, 50% glycerol, 0.05% Proclin 300, 0.05%BSA
Specificity
Endogenous
Purification
Protein A
Storage
-15°C to -25°C/1 year(Do not lower than -25°C)
MW(Calculated)
65kD
MW(Observed)
65kD
Modification
Unmodified
Clonality
Monoclonal
Clone Number
PT0125R
Isotype
IgG,Kappa
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Antigen&Target Information
Specificity:
Endogenous
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Gene Name:
CYBB
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Protein Name:
Cytochrome b-245 heavy chain
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Other Name:
CYBB ;
NOX2 ;
Cytochrome b-245 heavy chain ;
CGD91-phox ;
Cytochrome b ;
558 ;
subunit beta ;
Cytochrome b558 subunit beta ;
Heme-binding membrane glycoprotein gp91phox ;
NADPH oxidase 2Neutrophil cytochrome b 91 kDa polypeptide ;
Superoxide-generating NADPH oxidase heavy chain subunit ;
gp91-1 ;
gp91-phox ;
p22 phagocyte B-cytochrome
show all
Database Link:
Organism Gene ID SwissProt
Human 1536; P04839;
Mouse Q61093;
Background:
Cytochrome b (-245) is composed of cytochrome b alpha (CYBA) and beta (CYBB) chain. It has been proposed as a primary component of the microbicidal oxidase system of phagocytes. CYBB deficiency is one of five described biochemical defects associated with chronic granulomatous disease (CGD). In this disorder, there is decreased activity of phagocyte NADPH oxidase; neutrophils are able to phagocytize bacteria but cannot kill them in the phagocytic vacuoles. The cause of the killing defect is an inability to increase the cell's respiration and consequent failure to deliver activated oxygen into the phagocytic vacuole. [provided by RefSeq, Jul 2008],
Function:
cofactor:FAD.,Disease:Defects in CYBB are a cause of chronic granulomatous disease X-linked (XCGD) [MIM:306400]. Chronic granulomatous disease is a genetically heterogeneous disorder characterized by the inability of neutrophils and phagocytes to kill microbes that they have ingested. Patients suffer from life-threatening bacterial/fungal infections.,Function:Critical component of the membrane-bound oxidase of phagocytes that generates superoxide. It is the terminal component of a respiratory chain that transfers single electrons from cytoplasmic NADPH across the plasma membrane to molecular oxygen on the exterior. Also functions as a voltage-gated proton channel that mediates the H(+) currents of resting phagocytes. It participates in the regulation of cellular pH and is blocked by zinc.,online information:CYBB deficiency database,PTM:Glycosylated.,similarity:Contains 1 FAD-binding FR-type domain.,similarity:Contains 1 ferric oxidoreductase domain.,subunit:Composed of a heavy chain (beta) and a light chain (alpha).,
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Cellular Localization:
Membranous
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Tissue Expression:
Detected in neutrophils (at protein level).
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Research Areas:
>>HIF-1 signaling pathway ;
>>Phagosome ;
>>Ferroptosis ;
>>Necroptosis ;
>>Neutrophil extracellular trap formation ;
>>NOD-like receptor signaling pathway ;
>>Leukocyte transendothelial migration ;
>>AGE-RAGE signaling pathway in diabetic complications ;
>>Alzheimer disease ;
>>Prion disease ;
>>Pathways of neurodegeneration - multiple diseases ;
>>Leishmaniasis ;
>>Coronavirus disease - COVID-19 ;
>>Diabetic cardiomyopathy ;
>>Lipid and atherosclerosis
show all
Catalog: YM8068
Size
Price
Status
Qty.
200μL
$600.00
In stock

0

100μL
$340.00
In stock

0

40μL
$190.00
In stock

0

Add to cart

Collected

Collect

Customized Service

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