MANYEFSQVSGDRPGCRLSRKAQIGLGVGLLVLIALVVGIVVILLRPRSLLVWTGEPTTKHFSDIFLGRCLIYTQILRPEMRDQNCQEILSTFKGAFVSKNPCNITREDYAPLVKLVTQTIPCNKTLFWSKSKHLAHQYTWIQGKMFTLEDTLLGYIADDLRWCGDPSTSDMNYVSCPHWSENCPNNPITVFWKVISQKFAEDACGVVQVMLNGSLREPFYKNSTFGSVEVFSLDPNKVHKLQAWVMHDIEGASSNACSSSSLNELKMIVQKRNMIFACVDNYRPARFLQCVKNPEHPSCRLNT Note: The complete sequence including tag sequence, target protein sequence and linker sequence could be provided upon request.
蛋白標(biāo)簽:
N-terminal 10xHis-tagged
產(chǎn)品提供形式:
Liquid or Lyophilized powder Note: We will preferentially ship the format that we have in stock, however, if you have any special requirement for the format, please remark your requirement when placing the order, we will prepare according to your demand.
緩沖液:
Lyophilized from Tris/PBS-based buffer, 6% Trehalose, pH 8.0
儲(chǔ)存條件:
Store at -20°C/-80°C upon receipt, aliquoting is necessary for
mutiple use. Avoid repeated freeze-thaw cycles.
保質(zhì)期:
The shelf life is related to many factors, storage state,
buffer ingredients, storage temperature and the stability of the protein
itself.
Generally, the shelf life of liquid form is 6 months at -20°C/-80°C. The
shelf life of lyophilized form is 12 months at -20°C/-80°C.
貨期:
Basically, we can dispatch the products out in 1-3 working days after receiving your orders. Delivery time may differ from different purchasing way or location, please kindly consult your local distributors for specific delivery time.
Note: All of our
proteins are default shipped with normal blue ice packs, if you
request to ship with dry ice, please communicate with us in advance
and extra fees will be charged.
注意事項(xiàng):
Repeated freezing and thawing is not recommended. Store working aliquots at 4°C for up to one week.
Synthesizes the second messengers cyclic ADP-ribose and nicotinate-adenine dinucleotide phosphate, the former a second messenger for glucose-induced insulin secretion. Also has cADPr hydrolase activity.
基因功能參考文獻(xiàn):
Pathological and morphological screening of CD38-/- mouse brains reveals the involvement of CD38 in the development of the primary visual cortex and the hippocampus. Results show that the neuron count in the primary visual cortex and the dentate gyrus was significantly decreased, and pyramidal neurons in the visual cortex and hippocampus have an abnormal morphology. PMID: 29306053
our data are consistent with the conclusion that CD38 plays a role in murine and human lung tumorigenesis PMID: 29228209
CD38 deficiency significantly protected hearts from lipid-induced injury via regulating redox homeostasis, lipid metabolism and apoptosis in myocardial cells through activating Sirt3/FOXO3 signaling pathway. PMID: 30114710
these findings demonstrated a role of CD38 signaling pathway on the airway hyperresponsiveness of obesity PMID: 29414651
data demonstrate that CD38 represents a new marker that identifies committed preadipocytes as CD45(-) CD31(-) CD34(low) CD38(+) cells PMID: 28611394
Blockade of CD38 diminishes lipopolysaccharide-induced macrophage classical activation and acute kidney injury involving NF-kappaB signaling suppression. PMID: 29080804
the results presented in this study suggest that CD38 deficiency induces features of autoimmune disorders in aged mice and that CD38 could play a role in the control of autoimmune diseases through their expression on regulatory B cells. PMID: 29603313
CD38 plays an essential role in cardiac hypertrophy probably via inhibition of SIRT3 expression and activation of Ca(2+) -NFAT signaling pathway. PMID: 28296029
Determined the role of CD38, an enzyme involved in cellular calcium modulation and autophagic flux, in the regulation of collagen I degradation in coronary arterial myocytes (CAMs).In primary cultured CAMs from CD38(-/-) mice, collagen I protein accumulation but not mRNA abundance was significantly increased compared with cells from CD38(+/+) mice. PMID: 27814632
Data, including data from studies on cells from knockout mice, suggest that intracellular CD38 contributes to NAADP production and cADPR production in cardiomyocytes; membrane fractions from wildtype but not CD38-/- mouse hearts support NAADP and cADPR synthesis; CD38 may be associated with sarcoplasmic reticulum of cardiomyocytes. (NAADP = nicotinate adenine dinucleotide phosphate; cADPR = cyclic ADP-ribose) PMID: 28539361
These data provide the first experimental evidence that the proper function of CD38/nicotinic acid adenine dinucleotide phosphate pathway plays an essential role in promoting free cholesterol efflux. PMID: 26818887
expression and activity of the NADase CD38 increase with aging and that CD38 is required for the age-related NAD decline and mitochondrial dysfunction via a pathway mediated at least in part by regulation of SIRT3 activity. PMID: 27304511
Study found that deletion of CD38 caused impaired astrocytic and oligodendrocytic development in the cortex, probably by increasing NAD+ levels and decreasing Cx43 expression levels. PMID: 28295574
These results suggested that CD38 may be involved in the DC function of alleviating asthma via restoration of the Th1/Th2 balance, thus providing a novel strategy for asthma therapy. PMID: 27666020
CD38 deficiency protects the heart from ischemia/reperfusion injury through activating SIRT1/FOXOs-mediated antioxidative stress pathway. PMID: 27547294
Identification of multiple transferrin species in the spleen and serum from mice with collagen-induced arthritis which may reflect changes in transferrin glycosylation associated with disease activity: The role of CD38. PMID: 26639305
CD38 is critical for regulating hippocampus-dependent learning and memory without modulating synaptic plasticity. PMID: 26856703
CD38 signaling pathway is required for neuronal differentiation of embryonic stem cells by modulating reactive oxygen species production. PMID: 26012865
CD38/cADPR-mediated Ca(2+) signals play a key role in glucagon-induced gluconeogenesis in hepatocytes, and that the signal pathway has significant clinical implications in metabolic diseases, including type 2 diabetes. PMID: 26038839
CD38 is expressed in MDSCs in mouse models of esophageal carcinogenesis. CD38(high) MDSCs are immature, suggesting a potential role for CD38 in the maturation halt found in MDSC populations. IL6, IGFBP3, and CXCL16 induce CD38 expression by MDSCs ex vivo. PMID: 26294209
CD38 activation after NADPH depletion triggers endothelial dysfunction in the postischemic heart PMID: 26297248
In a model of Alzheimer disease, CD38 deficient mice had decreased amyloid-beta plaque burden, decreased microglia/macrophage accumulation, and better spatial learning. PMID: 25893674
sCD38 released from seminal vesicles to the seminal plasma acts as an immunoregulatory factor to protect semiallogeneic fetuses from maternal immune responses PMID: 25591581
These data demonstrate that B-cell precursors in mouse bone marrow express functional CD38 and implicate the early ligation of CD38 in the ERK-associated regulation of the B-lineage differentiation pathway. PMID: 25155483
Data show that CD38 knockout mice presented significant increases of cytokine mRNA expression, as well as liver damage after lipopolysaccharide (LPS)/D-galactosamine (D-GalN)-induced acute hepatic injury. PMID: 25270198
CD38 mediates microglial function and survival by mediating ATP release from microglia. PMID: 24578339
CD38 plays a critical role in autophagosome trafficking and fusion with lysosomes PMID: 24445604
CD38 in the nucleus accumbens and oxytocin are critical in paternal behavior. PMID: 24059452
Renal vasoconstriction by vasopressin V1a receptors is modulated by nitric oxide, prostanoids, and superoxide but not the ADP ribosyl cyclase CD38. PMID: 24623148
CD38 importantly control lysosomal function and influence autophagy at the maturation step in podocytes. PMID: 24238063
results suggest that SNPs in CD38 may be possible risk factors for autism spectrum disorders (ASD) by abrogating oxytocin (OXT) function and that some ASD subjects can be treated with OXT in preliminary clinical trials PMID: 22366648
The CD38/cADPR signaling pathway may be one underlying mechanism of the glucose and insulin effects of the alpha-2 adrenergic receptor agonist medetomidine and likely other drugs of its class. PMID: 23565906
NOX1-dependent superoxide production mediates CD38 internalization in coronary arterial myocytes. PMID: 23940720
In conclusion, these results demonstrate an essential role for CD38 in the innate immune response against Listeria monocytogenes. PMID: 23980105
CD38-cADPR mediates bile acid-induced pancreatitis and acinar cell injury through aberrant intracellular Ca(2+) signaling. PMID: 23940051
PECAM1(+)/Sca1(+)/CD38(+) vascular cells could proliferate and differentiate into myofibroblast-like cells in wound repair. PMID: 23308177
These results show that CD38 is a novel pharmacological target to treat metabolic diseases via NAD(+)-dependent pathways. PMID: 23172919
The tetrameric interaction underlies the multifaceted actions of CD38. PMID: 22863568
the CD38-cADPR-Ca(2+) signaling pathway antagonizes the CM differentiation of mouse ES cells. PMID: 22908234
The normal expression of CD38 importantly contributes to the differentiation and function of podocytes. PMID: 21992601
Our results thus suggest that CD38 participates in the tumor-supporting action of glioma-infiltrating microglia and macrophages PMID: 22700727
CD38 participates in the pathogenesis of collagen-induced arthritis controlling the number of iNKT cells and promoting Th1 inflammatory responses. PMID: 22438945
a crucial role of CD38 in FcgammaR-mediated phagocytosis through its recruitment to the phagosome and mobilization of cADPR-induced intracellular Ca(2+) and store-operated extracellular Ca(2+) influx. PMID: 22396532
we review the functional roles of cyclic ADP-ribose and CD38, a transmembrane protein with ADP-ribosyl cyclase activity, in mouse social behavior via the regulation of oxytocin (OXT) release--REVIEW PMID: 22227279
direct evidence that the CD38 cyclic ADP ribose pathway is an important controller of Nox4-mediated intracellular superoxide production PMID: 22100343
CD38 plays a critical role in the basal survival of microglia, and decreased CD38 can lead to caspase 3-dependent apoptosis of the cells. PMID: 22293203
CD38 contributes to behavioral and metabolic circadian rhythms and altered NAD(+) levels influence the circadian clock. PMID: 21937766
In conclusion, CD38 is important for neutrophils migration during hepatic amoebiasis, and in turn, these cells play an important role in the innate immune response. PMID: 21919917
In vivo CD38 appears to be a NAADP degrading rather than a NAADP forming enzyme PMID: 22020217
The myocardial contractility, contraction and relaxation velocities were significantly enhanced only in male CD38-null mice, in which the levels of serum testosterone were markedly elevated. PMID: 21840325