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Recombinant Human TSLP Protein

  • 表达系统: E. coli
  • Accession #: Q969D9
  • 蛋白标签: N-His
  • 生物活性: Immobilized Recombinant Human TSLP Protein (rp169653) at 2.0 μg/mL can bind Tezepelumab (anti-TSLP) (Ab170833) with the EC50 of 18.04 ng/mL.
  • 内毒素水平: <1.0 EU/μg
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货号 (SKU) 包装规格 是否现货 价格 数量
rp169653-10μg
10μg 现货 Stock Image
rp169653-50μg
50μg 现货 Stock Image
rp169653-100μg
100μg 期货 Stock Image
rp169653-1mg
1mg 期货 Stock Image

基本描述

产品名称 Recombinant Human TSLP Protein
别名 重组人TSLP蛋白 | 重组人 TSLP 蛋白
英文别名 thymic stromal lymphopoietin | TSLP | Thymic stromal lymphopoietin protein TSLP | TSLP protein | TSLP_HUMAN | EC 1.3.5.1 | Ip | Iron-sulfur subunit of complex II
规格或纯度 ActiBioPure™, Bioactive, Carrier Free, Azide Free, ≥95%(SDS-PAGE)
产品介绍


Purity:>95%, by SDS-PAGE visualized with Coomassie® Blue Staining.
Description:
Thymic stromal lymphopoietin (TSLP) is an interleukin 7 (IL-7)-like cytokine originally characterized by its ability to promote the activation of B cells and dendritic cells (DCs). Thymic stromal lymphopoietin (TSLP) is a cytokine expressed by epithelial cells, including keratinocytes, and is important in allergic inflammation. Subsequent studies have shown that TSLP promotes T helper type 2 (TH2) cell responses associated with immunity to some helminth parasites and the pathogenesis of many inflammatory diseases, including atopic dermatitis and asthma. TSLP can promote TH2 cytokine-associated inflammation by directly promoting the effector functions of CD4+ TH2 cells, basophils and other granulocyte populations while simultaneously limiting the expression of DC-derived proinflammatory cytokines and promoting regulatory T cell responses in peripheral tissues.

生物活性 Immobilized Recombinant Human TSLP Protein (rp169653) at 2.0 μg/mL can bind Tezepelumab (anti-TSLP) (Ab170833) with the EC50 of 18.04 ng/mL.
内毒素水平 <1.0 EU/μg
表达系统 E. coli
种属 人(Human)
氨基酸 29-159 aa
序列 MGSSHHHHHHSSGLVPRGSYDFTNCDFEKIKAAYLSTISKDLITYMSGTKSTEFNNTVSCSNRPHCLTEIQSLTFNPTAGCASLAKEMFAMKTKAALAIWCPGYSETQINATQAMKKRRKRKVTTNKCLEQVSQLQGLWRRFNRPLLKQQ
纯度 >95%(SDS-PAGE)
蛋白标签 N-His
无载体 Yes
无动物源 No
Accession # Q969D9
来源 重组表达
预测分子量 17.0 kDa
SDS-PAGE 15.4 kDa, reducing conditions

储存与运输

物理形态 透明胶状
储存缓冲液 Lyophilized from PBS, 2.5%Glycerol, 1mM EDTA, pH7.4
复溶 We recommend that this vial be briefly centrifuged prior to opening to bring the contents to the bottom. Reconstitute at 0.1 mg/mL in sterile distilled water. Stock solutions should be apportioned into working aliquots and stored at ≤ -20 °C. Further dilutions should be made in appropriate buffered solutions.
储存温度 -20°C储存,避免反复冻融
运输条件 超低温冰袋运输
稳定性与储存 在 -20°C 下可保存 1 年。避免冷冻/解冻循环。
分子类型 蛋白质

图片

Recombinant Human TSLP Protein (rp169653) - SDS-PAGE
Recombinant Human TSLP Protein was resolved with SDS-PAGE under reducing (R) conditions and visualized by Coomassie® Blue staining, showing a band at 15.4 kDa.

Recombinant Human TSLP Protein (rp169653) - ELISA
Immobilized Recombinant Human TSLP Protein (rp169653) at 2.0 μg/mL can bind Tezepelumab (anti-TSLP) (Ab170833) with the EC₅₀ of 18.04 ng/mL.

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找到3个结果

批号(Lot Number) 证书类型 货号
ZJ23F1101771 分析证书 rp169653
ZJ23F1101772 分析证书 rp169653
ZJ23F1101773 分析证书 rp169653

引用文献

1. Kita, K K, Oya, H H, Gennis, R B RB, Ackrell, B A BA and Kasahara, M M..  (1990)  Human complex II (succinate-ubiquinone oxidoreductase): cDNA cloning of iron sulfur (Ip) subunit of liver mitochondria..  Biochemical and biophysical research communications,  (15): [PMID:2302193]
2. Gould, S J SJ, Subramani, S S and Scheffler, I E IE..  (1989)  Use of the DNA polymerase chain reaction for homology probing: isolation of partial cDNA or genomic clones encoding the iron-sulfur protein of succinate dehydrogenase from several species..  Proceedings of the National Academy of Sciences of the United States of America,  [PMID:2494655]
3. Au, H C HC and 5 more authors..  (1995)  Structural organization of the gene encoding the human iron-sulfur subunit of succinate dehydrogenase..  Gene,  (4): [PMID:7622059]
4. Astuti, D D and 9 more authors..  (2001)  Gene mutations in the succinate dehydrogenase subunit SDHB cause susceptibility to familial pheochromocytoma and to familial paraganglioma..  American journal of human genetics,  [PMID:11404820]
5. Baysal, B E BE and 11 more authors..  (2002)  Prevalence of SDHB, SDHC, and SDHD germline mutations in clinic patients with head and neck paragangliomas..  Journal of medical genetics,  [PMID:11897817]
6. Neumann, Hartmut P H HP and 29 more authors..  (2002)  Germ-line mutations in nonsyndromic pheochromocytoma..  The New England journal of medicine,  (9): [PMID:12000816]
7. Young, Abbie L AL, Baysal, Bora E BE, Deb, Arjun A and Young, William F WF..  (2002)  Familial malignant catecholamine-secreting paraganglioma with prolonged survival associated with mutation in the succinate dehydrogenase B gene..  The Journal of clinical endocrinology and metabolism,  [PMID:12213855]
8. Benn, Diana E DE and 9 more authors..  (2003)  Novel succinate dehydrogenase subunit B (SDHB) mutations in familial phaeochromocytomas and paragangliomas, but an absence of somatic SDHB mutations in sporadic phaeochromocytomas..  Oncogene,  (6): [PMID:12618761]
9. Gimenez-Roqueplo, Anne-Paule AP and 10 more authors..  (2003)  Mutations in the SDHB gene are associated with extra-adrenal and/or malignant phaeochromocytomas..  Cancer research,  (1): [PMID:14500403]
10. Maier-Woelfle, Margarete M and 10 more authors..  (2004)  A novel succinate dehydrogenase subunit B gene mutation, H132P, causes familial malignant sympathetic extraadrenal paragangliomas..  The Journal of clinical endocrinology and metabolism,  [PMID:14715873]
11. Astuti, Dewi D and 13 more authors..  (2003)  Genetic analysis of mitochondrial complex II subunits SDHD, SDHB and SDHC in paraganglioma and phaeochromocytoma susceptibility..  Clinical endocrinology,  [PMID:14974914]
12. Neumann, Hartmut P H HP and 16 more authors..  (2004)  Distinct clinical features of paraganglioma syndromes associated with SDHB and SDHD gene mutations..  JAMA,  (25): [PMID:15328326]
13. McDonnell, Ciara M CM, Benn, Diana E DE, Marsh, Deborah J DJ, Robinson, Bruce G BG and Zacharin, Margaret R MR..  (2004)  K40E: a novel succinate dehydrogenase (SDH)B mutation causing familial phaeochromocytoma and paraganglioma..  Clinical endocrinology,  [PMID:15473885]
14. Kullberg, Morgan M, Nilsson, Maria A MA, Arnason, Ulfur U, Harley, Eric H EH and Janke, Axel A..  (2006)  Housekeeping genes for phylogenetic analysis of eutherian relationships..  Molecular biology and evolution,  [PMID:16751257]
15. van Nederveen, Francien H FH, Korpershoek, Esther E, Lenders, Jacques W M JW, de Krijger, Ronald R RR and Dinjens, Winand N M WN..  (2007)  Somatic SDHB mutation in an extraadrenal pheochromocytoma..  The New England journal of medicine,  (19): [PMID:17634472]
16.  (2007)  Familial gastrointestinal stromal tumors and germ-line mutations..  The New England journal of medicine,  (6): [PMID:17804857]
17. Ni, Ying Y and 9 more authors..  (2008)  Germline mutations and variants in the succinate dehydrogenase genes in Cowden and Cowden-like syndromes..  American journal of human genetics,  [PMID:18678321]
18. Alston, Charlotte L CL and 12 more authors..  (2012)  Recessive germline SDHA and SDHB mutations causing leukodystrophy and isolated mitochondrial complex II deficiency..  Journal of medical genetics,  [PMID:22972948]
19. Helman, Guy G and 13 more authors..  (2016)  Magnetic resonance imaging spectrum of succinate dehydrogenase-related infantile leukoencephalopathy..  Annals of neurology,  [PMID:26642834]
20. Maio, Nunziata N and 9 more authors..  (2016)  Disease-Causing SDHAF1 Mutations Impair Transfer of Fe-S Clusters to SDHB..  Cell metabolism,  (9): [PMID:26749241]
21. Ardissone, Anna and 5 more authors..  (2015)  Mitochondrial leukoencephalopathy and complex II deficiency associated with a recessive SDHB mutation with reduced penetrance..  Molecular genetics and metabolism reports,  [PMID:26925370]
22. Grønborg, Sabine S and 10 more authors..  (2017)  Leukoencephalopathy due to Complex II Deficiency and Bi-Allelic SDHB Mutations: Further Cases and Implications for Genetic Counselling..  JIMD reports,  [PMID:27604842]
23. Kaur, Parneet; Sharma, Suvasini; Kadavigere, Rajagopal; Girisha, Katta Mohan and Shukla, Anju..  (2020)  Novel variant p.(Ala102Thr) in SDHB causes mitochondrial complex II deficiency: Case report and review of the literature..  Annals of human genetics,  [PMID:32124427]
24. Saribas, Sami and Safak, Mahmut..  (2020)  A Comprehensive Proteomics Analysis of the JC Virus (JCV) Large and Small Tumor Antigen Interacting Proteins: Large T Primarily Targets the Host Protein Complexes with V-ATPase and Ubiquitin Ligase Activities While Small t Mostly Associates with Those Having Phosphatase and Chromatin-Remodeling Functions..  Viruses,  (20): [PMID:33092197]

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