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

KANSL1 Antibody

  • 中文名稱:
    KANSL1兔多克隆抗體
  • 貨號:
    CSB-PA770344LA01HU
  • 規格:
    ¥440
  • 圖片:
    • Immunohistochemistry of paraffin-embedded human testis tissue using CSB-PA770344LA01HU at dilution of 1:100
    • Immunofluorescent analysis of A549 cells using CSB-PA770344LA01HU at dilution of 1:100 and Alexa Fluor 488-congugated AffiniPure Goat Anti-Rabbit IgG(H+L)
  • 其他:

產品詳情

  • 產品名稱:
    Rabbit anti-Homo sapiens (Human) KANSL1 Polyclonal antibody
  • Uniprot No.:
  • 基因名:
    KANSL1
  • 別名:
    CENP-36 antibody; centromere protein 36 antibody; DKFZp686P06109 antibody; DKFZp727C091 antibody; hMSL1v1 antibody; hypothetical protein LOC284058 antibody; K1267_HUMAN antibody; KANSL1 antibody; KAT8 regulatory NSL complex subunit 1 antibody; KDVS antibody; KIAA1267 antibody; male-specific lethal 1 homolog antibody; MGC102843 antibody; MLL1/MLL complex subunit KIAA1267 antibody; MSL1 homolog 1 antibody; MSL1v1 antibody; Non specific lethal 1 homolog antibody; NSL complex protein NSL1 antibody; NSL1 antibody
  • 宿主:
    Rabbit
  • 反應種屬:
    Human
  • 免疫原:
    Recombinant Human KAT8 regulatory NSL complex subunit 1 protein (815-1086AA)
  • 免疫原種屬:
    Homo sapiens (Human)
  • 標記方式:
    Non-conjugated

    本頁面中的產品,KANSL1 Antibody (CSB-PA770344LA01HU),的標記方式是Non-conjugated。對于KANSL1 Antibody,我們還提供其他標記。見下表:

    可提供標記
    標記方式 貨號 產品名稱 應用
    HRP CSB-PA770344LB01HU KANSL1 Antibody, HRP conjugated ELISA
    FITC CSB-PA770344LC01HU KANSL1 Antibody, FITC conjugated
    Biotin CSB-PA770344LD01HU KANSL1 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, IHC, IF
  • 推薦稀釋比:
    Application Recommended Dilution
    IHC 1:20-1:200
    IF 1:50-1:200
  • Protocols:
  • 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:
    As part of the NSL complex it is involved in acetylation of nucleosomal histone H4 on several lysine residues and therefore may be involved in the regulation of transcription.
  • 基因功能參考文獻:
    1. These results show that a KANSL1 microduplication, in combination with the 22q11.2 deletion, is associated with increased risk of CHD in these patients, suggesting that KANSL1 plays a role as a modifier gene in 22q11.2DS patients. PMID: 28496102
    2. One variant, p.Lys104Thr, was predicted damaging and appeared overrepresented in our 90-patient cohort compared to Genome Aggregation Database allele frequency (0.217 to 0.116). However, there was no difference in p.Lys104Thr allele frequency in the follow-up childhood epilepsy with centrotemporal spikes (CECTS) and atypical childhood epilepsy with centrotemporal spikes (ACECTS) cohort and controls. PMID: 29352316
    3. This case expands the mild end of the neurodevelopmental spectrum seen in children with de novo KANSL1 mutation and KdVS. PMID: 28211987
    4. In KANSL1 haploinsufficiency syndrome, chromosome deletions are greatly prevalent compared with KANSL1 mutations. PMID: 26424144
    5. essential for mitotic spindle assembly and chromosome segregation PMID: 26243146
    6. KANSL1 gene haploinsufficiency is necessary and sufficient to cause the full spectrum of the 17q21.31 microdeletion syndrome. PMID: 26293599
    7. findings show that de novo loss-of-function mutations in KANSL1 cause a full del(17q21.31) phenotype in 2 unrelated individuals that lack deletion at 17q21.31; findings indicate that 17q21.31 deletion syndrome is a monogenic disorder caused by haploinsufficiency of KANSL1 PMID: 22544367
    8. Observational study of gene-disease association. (HuGE Navigator) PMID: 18509094

    顯示更多

    收起更多

  • 亞細胞定位:
    Nucleus. Nucleus. Chromosome, centromere, kinetochore.
  • 組織特異性:
    Expressed in the brain.
  • 數據庫鏈接:

    HGNC: 24565

    OMIM: 612452

    KEGG: hsa:284058

    STRING: 9606.ENSP00000262419

    UniGene: Hs.648744



主站蜘蛛池模板: 精品无码日韩一区二区三区不卡| 男人j进入女人j内部免费网站| 国产激情久久久久久熟女老人av | 樱花草在线社区www| 日韩精品人妻系列一区二区三区 | 成人无遮挡裸免费视频在线观看 | 窝窝午夜理论片影院| 99蜜桃在线观看免费视频网站| 无码动漫性爽xo视频在线观看 | 欧洲 亚洲 国产图片综合| 久青草久青草视频在线观看 | 18禁又污又黄又爽的网站不卡| 欧洲精品99毛片免费高清观看| 亚洲aⅴ天堂av天堂无码麻豆| 少妇高潮喷水在线观看| 亚洲一卡2卡三卡4卡国色天香| 99精品国产一区二区三区不卡 | av天堂午夜精品蜜臀av| 亚洲色欧美色2019在线| 8av国产精品爽爽ⅴa在线观看| 久久综合狠狠综合久久综| 又嫩又硬又黄又爽的视频| 玩弄人妻少妇精品视频| 无码吃奶揉捏奶头高潮视频| 久久被窝亚洲精品爽爽爽| 大地资源中文第三页| 日韩精品中文字幕无码专区 | 国产成人一区二区青青草原| 国产女人好紧好爽| 日韩精品一卡2卡三卡4卡| 亚洲日韩中文字幕久热| 影音先锋男人av鲁色资源网| 成人影片麻豆国产影片免费观看| 日日摸日日碰夜夜爽免费| 国产初高中生真实在线视频 | 亚洲精品久久av无码一区二区 | 久久久久99精品成人片直播| 国产熟女亚洲精品麻豆| 日本三级欧美三级人妇视频| 香港aa三级久久三级| av中文字幕潮喷人妻系列|