在线日韩日本国产亚洲丨少妇伦子伦情品无吗丨欧美性猛交xxxx免费看蜜桃丨精品人妻系列无码一区二区三区丨亚洲精品无码不卡在线播放

Your Good Partner in Biology Research

  1. 首頁
  2. 蛋白
  3. 重組蛋白
  4. Recombinant Human Caspase recruitment domain-containing protein 14 (CARD14), partial

Recombinant Human Caspase recruitment domain-containing protein 14 (CARD14), partial

  • 中文名稱：
    Recombinant Human Caspase recruitment domain-containing protein 14(CARD14) ,partial
  • 貨號：
    CSB-YP883622HU
  • 規格：
  • 來源：
    Yeast
  • 其他：
  • 中文名稱：
    Recombinant Human Caspase recruitment domain-containing protein 14(CARD14) ,partial
  • 貨號：
    CSB-EP883622HU
  • 規格：
  • 來源：
    E.coli
  • 其他：
  • 中文名稱：
    Recombinant Human Caspase recruitment domain-containing protein 14(CARD14) ,partial
  • 貨號：
    CSB-EP883622HU-B
  • 規格：
  • 來源：
    E.coli
  • 共軛：
    Avi-tag Biotinylated

    E. coli biotin ligase (BirA) is highly specific in covalently attaching biotin to the 15 amino acid AviTag peptide. This recombinant protein was biotinylated in vivo by AviTag-BirA technology, which method is BriA catalyzes amide linkage between the biotin and the specific lysine of the AviTag.

  • 其他：
  • 中文名稱：
    Recombinant Human Caspase recruitment domain-containing protein 14(CARD14) ,partial
  • 貨號：
    CSB-BP883622HU
  • 規格：
  • 來源：
    Baculovirus
  • 其他：
  • 中文名稱：
    Recombinant Human Caspase recruitment domain-containing protein 14(CARD14) ,partial
  • 貨號：
    CSB-MP883622HU
  • 規格：
  • 來源：
    Mammalian cell
  • 其他：

產品詳情

  • 純度：
    >85% (SDS-PAGE)
  • 基因名：
  • Uniprot No.：
  • 別名：
    Bcl10 interacting MAGUK protein 2; Bimp 2; Bimp2 ; CAR14_HUMAN; CARD 14; CARD containing MAGUK 2 protein; CARD containing MAGUK protein 2; Card maguk protein 2; CARD-containing MAGUK protein 2; CARD14; Carma 2; Carma2; Caspase recruitment domain containing protein 14; Caspase recruitment domain family member 14; Caspase recruitment domain protein 14; Caspase recruitment domain-containing protein 14; PRP; PSORS2; PSS1
  • 種屬：
    Homo sapiens (Human)
  • 蛋白長度：
    Partial
  • 蛋白標簽：
    Tag?type?will?be?determined?during?the?manufacturing?process.
    The tag type will be determined during production process. If you have specified tag type, please tell us and we will develop the specified tag preferentially.
  • 產品提供形式：
    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.
  • 復溶：
    We recommend that this vial be briefly centrifuged prior to opening to bring the contents to the bottom. Please reconstitute protein in deionized sterile water to a concentration of 0.1-1.0 mg/mL.We recommend to add 5-50% of glycerol (final concentration) and aliquot for long-term storage at -20℃/-80℃. Our default final concentration of glycerol is 50%. Customers could use it as reference.
  • 儲存條件：
    Store at -20°C/-80°C upon receipt, aliquoting is necessary for mutiple use. Avoid repeated freeze-thaw cycles.
  • 保質期：
    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：
    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：
    Repeated freezing and thawing is not recommended. Store working aliquots at 4°C for up to one week.
  • Datasheet ：
    Please contact us to get it.

產品評價

靶點詳情

  • 功能：
    Acts as a scaffolding protein that can activate the inflammatory transcription factor NF-kappa-B and p38/JNK MAP kinase signaling pathways. Forms a signaling complex with BCL10 and MALT1, and activates MALT1 proteolytic activity and inflammatory gene expression. MALT1 is indispensable for CARD14-induced activation of NF-kappa-B and p38/JNK MAP kinases. May play a role in signaling mediated by TRAF2, TRAF3 and TRAF6 and protects cells against apoptosis.; Not able to activate the inflammatory transcription factor NF-kappa-B and may function as a dominant negative regulator.
  • 基因功能參考文獻：
    1. Results identified RNF7 to interact with CARMA2 regulating its NF-kappaB-activating capacity. Mechanistically, RNF7 influences CARMA2 signaling by regulating the ubiquitination state of MALT1 and the NF-kappaB-regulatory molecule NEMO. Interestingly, CARMA2short (CARMA2sh) mutants associated with psoriasis susceptibility escape the negative control exerted by RNF7. PMID: 29194363
    2. The serine/threonine kinase ULK2 binds to and phosphorylates CARMA2sh. PMID: 28230860
    3. MALT1 deficiency or pharmacological inhibition of MALT1 catalytic activity inhibits pathogenic mutant CARD14-induced cytokine and chemokine expression in human primary keratinocytes. PMID: 27113748
    4. CARD14/MALT1-mediated signaling in keratinocytes has a role in psoriasis [review] PMID: 27939769
    5. The results indicate that the common CARD14 p.Arg820Trp variant might have a significant effect on the response to anti-TNF therapies among patients with psoriasis. In addition, rare CARD14 missense variants could also predispose to a better response. PMID: 26854129
    6. Our findings, combined with the published literature, suggest that Pityriasis Rubra Pilaris Type V, both familial and sporadic, can be caused by CARD14 mutations. PMID: 27760266
    7. Psoriasis mutations disrupt CARD14 autoinhibition promoting BCL10-MALT1-dependent NF-kappaB activation PMID: 27071417
    8. genetic evidence suggests association of the CARD14 single nucleotide polymorphism rs11652075 and other rare mutations in this gene with psoriasis. To assess whether combined data support the relationship between CARD14 rs11652075 and susceptibility to this disease, we conducted a meta-analysis. Our results demonstrate a significant association between the CARD14 rs11652075 polymorphism and psoriasis. PMID: 27706581
    9. SNP c.C2458T may have significant effects on heritability of psoriasis vulgaris in our Chinese population. The CC genotype was more common in familial cases than in sporadic cases. PMID: 26249641
    10. The authors observations provide further insights into the genetics of psoriasis and functional information on novel CARD14 mutational variants seen in cases from Tunisia and other populations. PMID: 26358359
    11. Genetic interactions of SNPs in CARD14, SENP1 and VEGFA might represent a functional mechanism in the pathogenesis of high altitude polycythemia. PMID: 26852650
    12. We found five rare mutations and four of them are annotated or reported. Only the variant (c.1291C>G) has not been reported and annotated, but the variant was also found in controls. None of the new definite variants were pathogenic PMID: 26982778
    13. analysis of 105 individuals with generalized pustular psoriasis (GPP) identified a low-frequency variant (p.Asp176His) that causes constitutive CARD14 oligomerization PMID: 26203641
    14. CARD14 protein missense mutation found in patients diagnosed with psoriasis. PMID: 25989471
    15. no definite causative genetic mutation in CARD14 as identified in familial pityriasis rubra pilaris after screening 8 non-familial patients of type I, type III and type IV pityriasis rubra pilaris PMID: 24577624
    16. The study identified the DEP domain-containing protein DEPDC7 as cellular binding partner of CARMA2 and CARMA3 proteins. PMID: 25541973
    17. CARD14 mutation maybe responsible for activation of NF-kB signaling pathway in patients with pityriasis rubra pilaris. PMID: 25734815
    18. Transfection of dermal ECs with psoriasis-associated CARD14 mutations resulted in increased expression of several chemokines, including CXCL10, IL-8, and CCL2. PMID: 25369198
    19. Variant analysis of CARD14 in a Chinese Han population with psoriasis vulgaris and generalized pustular psoriasis shows that CARD14 may play a role in the pathogenesis of generalized pustular psoriasis. PMID: 24999592
    20. Owing to the relatively small number of cases analysed in this study, we cannot rule out the possibility that CARD14 mutations may be an exceptional cause of sporadic pityriasis rubra pilaris, as previously found in sporadic psoriasis PMID: 24359224
    21. Mutations and variants are causal or disease susceptibility factors of psoriasis vulgaris, generalized pustular psoriasis, or pityriasis rubra pilaris. [review] PMID: 24656634
    22. Chromosome 17q25 harbors a susceptibility locus for psoriasis. Non-parametric linkage analysis revealed a linkage peak lying close to a novel cluster of genes from the immunoglobulin (Ig) superfamily. PMID: 12483297
    23. Our results confirmed the published linkage with the PSORS1 locus, as well as the PSORS2 locus, which has not been previously shown in the Chinese population. PMID: 12709815
    24. These results fail to support rs734232 as a psoriasis susceptibility factor in German psoriasis patients. PMID: 15654961
    25. PSORS2 alleles are not susceptibility factors in arthritis psoriatic patients of Italian origin PMID: 16733365
    26. Results show genetic heterogeneity of psoriasis in the Tunisian population, provide confirmatory evidence for a novel psoriasis locus at chromosome 2p12 and reveal a psoriasis family with a mutation at PSORS2. PMID: 23013406
    27. Pityriasis rubra pilaris autosomal dominant family is an allelic disease to certain genetic forms of familial psoriasis. PMID: 23328365
    28. CARD14 c.526G>C (p.Asp176His) may have a role in generalized pustular psoriasis with psoriasis vulgaris in Japanese patients PMID: 24476623
    29. the association between SNP rs11652075 at the CARD14 gene and psoriasis PMID: 23905699
    30. we identified three different heterozygous mutations in CARD14 causing familial pityriasis rubra pilaris. PMID: 22703878
    31. Here, rare, highly penetrant mutations in CARD14 have been shown to cause psoriasis. PMID: 22521418
    32. A range of NF-kB responses in the skin are mediated by CARD14 and that a subset of rare CARD14 variants leads to psoriasis and psoriatic arthritis. PMID: 22521419
    33. Results demonstrate that multiple transcripts encoding several CARMA2 isoforms exist in vivo and regulate NF-kappaB activation and apoptosis. PMID: 21302310

    顯示更多

    收起更多

  • 相關疾病：
    Psoriasis 2 (PSORS2); Pityriasis rubra pilaris (PRP)
  • 亞細胞定位：
    [Isoform 1]: Cytoplasm.; [Isoform 2]: Cytoplasm.; [Isoform 3]: Cytoplasm.
  • 組織特異性：
    Isoform 1 is detected in placenta and epidermal keratinocytes. Isoform 2 is detected in leukocytes and fetal brain.
  • 數據庫鏈接：

    HGNC: 16446

    OMIM: 173200

    KEGG: hsa:79092

    STRING: 9606.ENSP00000344549

    UniGene: Hs.675480



主站蜘蛛池模板： 宅男666在线永久免费观看| 中文无码乱人伦中文视频在线| ww国产内射精品后入国产| 特级无码毛片免费视频播放▽| 日韩av毛片无码免费| 久久精品人人做人人爽97| 天天狠天天透天干天天怕∴| 一线二线三线天堂| 日韩去日本高清在线| 在线不卡av片免费观看| 色偷偷偷在线视频播放| 无码gogo大胆啪啪艺术 | 99国产精品人妻噜啊噜| 免费视频爱爱太爽了激情| 一边做一边喷17p亚洲乱妇50p| 精品人妻无码区二区三区| 欧美性大战xxxxx久久久| 国产精品激情欧美可乐视频| 亚洲国产精品无码中文字| 久久人人爽人人爽人人片av高清| 免费无码不卡视频在线观看| 性欧美俄罗斯极品| 久久久99精品成人片中文字幕| 亚洲精品天堂成人片av在线播放| 99久久国语露脸精品国产| 人妻丝袜无码国产一区| 久久香蕉国产线看观看猫咪av| 噜妇插内射精品| 亚洲另类欧美综合在线| 成人乱码一区二区三区四区| 欧美激情a∨在线视频播放| 国产女人爽的流水毛片| 亚洲婷婷五月激情综合app| 欧美性受xxxx狂喷水| 国产精品美女久久久久| 欧美亚洲熟妇一区二区三区| 国产精品美女久久久久| 久久精品国产99久久久古代| 精品久久久久久久久午夜福利| 动漫精品中文无码卡通动漫| 国产卡一卡二卡三无线乱码新区|