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: 日本高清在线www3344| 一区二区乱子伦在线播放| 亚洲日韩av一区二区三区四区 | 国产亚洲精品久久久久久大师| 青草伊人久久综在合线亚洲观看| 无码国产一区二区三区四区| 丝袜高潮流白浆潮喷在线播放| 成人久久久久久久久久久| 精品高潮呻吟99av无码视频| 内射少妇36p亚洲区| 国产欧美另类久久久精品图片| 国产成人无码精品久久涩吧| 国产在线视频一区二区三区98| 国自产偷精品不卡在线| 老司机午夜福利视频| 久久久亚洲欧洲日产av| 国产午夜精品一二区理论影院| 在线播放午夜理论片| 同性男男黄g片免费网站| 暖暖 在线 日本 免费 中文| 在线高清亚洲精品二区| 亚洲欧美在线观看品| 国产成人无码a区在线观看视频| 欧美激情性做爰免费视频| 国产成人午夜福利在线观看| 亚洲精品国产一区二区精华| 成人一区二区免费视频| 无码国产色欲xxxx视频| 伊人久久大香线蕉亚洲| 亚洲国产成人精品无码一区二区 | 久久久久中文伊人久久久| 免费无码国产欧美久久18| 色欲av永久无码精品无码蜜桃| 天天爱天天做天天做天天吃中文 | 亚洲一卡2卡三卡四卡精品| 亚洲成在线aⅴ免费视频| 国产美女精品视频线免费播放软件| 国产sm重味一区二区三区| 人妻丝袜中文无码av影音先锋专区 | 一本色道久久综合狠狠躁篇| 无码国内精品久久综合88|