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

ILDR1 Antibody, FITC conjugated

  • 中文名稱:
    ILDR1兔多克隆抗體, FITC偶聯
  • 貨號:
    CSB-PA768201LC01HU
  • 規格:
    ¥880
  • 其他:

產品詳情

  • 產品名稱:
    Rabbit anti-Homo sapiens (Human) ILDR1 Polyclonal antibody
  • Uniprot No.:
  • 基因名:
    ILDR1
  • 別名:
    ILDR1 antibody; Immunoglobulin-like domain-containing receptor 1 antibody
  • 宿主:
    Rabbit
  • 反應種屬:
    Human
  • 免疫原:
    Recombinant Human Immunoglobulin-like domain-containing receptor 1 protein (393-541AA)
  • 免疫原種屬:
    Homo sapiens (Human)
  • 標記方式:
    FITC
  • 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
  • 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:
    Putative membrane receptor.
  • 基因功能參考文獻:
    1. The study shows that the novel p.G141R mutation in ILDR1 is the likely genetic cause for the hearing impairment in two unrelated Chinese Han DFNB42 families. PMID: 29849566
    2. this is the first ILDR1 and MYO6 mutations recognized in the southwest Iran. Our data expands the spectrum of mutations in ILDR1 and MYO6 genes. PMID: 29224747
    3. The present study reports a first ILDR1 gene mutation in a consanguineous family with hearing loss in the UAE, and confirms that the whole-exome sequencing approach is a robust tool for the diagnosis of monogenic diseases with high levels of allelic and locus heterogeneity. PMID: 28945813
    4. We discovered two genome-wide significant SNPs. The first was novel and near ISG20. The second was in TRIOBP, a gene previously associated with prelingual nonsyndromic hearing loss. Motivated by our TRIOBP results, we also looked at exons in known hearing loss genes, and identified two additional SNPs, rs2877561 in ILDR1 and rs9493672 in EYA4 (at a significance threshold adjusted for number of SNPs in those regions). PMID: 27764096
    5. consanguineous deaf families with novelmutations in the ILDR1 gene, were identified. PMID: 26440088
    6. Whole-exome sequencing of a Korean multiplex family segregating partial deafness identified a novel homozygous ILDR1 variant (p.P69H) within the Ig-like domain. PMID: 25668204
    7. Data indicate a mutation in immunoglobulin-like domain containing receptor 1 (ILDR1) as a causative gene for autosomal-recessive non-syndromic hearing loss (arNSHL) in a consanguineous Saudi family with three affected children. PMID: 24768815
    8. The findings show the heterogeneity of the molecular organization of tTJs in terms of the content of LSR, ILDR1 or ILDR2, and suggest that ILDR1-mediated recruitment of tricellulin to TCs is required for hearing. PMID: 23239027
    9. The analysis of gene expression was extended to Refractory Anemia (RA) and Refractory Anemia with excess blasts (RAEB) cases revealing ILDR1 overexpression in 36% of RAEB subgroup. PMID: 22365942
    10. Loss-of-function mutations of ILDR1 cause autosomal-recessive hearing impairment DFNB42. PMID: 21255762
    11. Clinical trial of gene-disease association and gene-environment interaction. (HuGE Navigator) PMID: 20379614

    顯示更多

    收起更多

  • 相關疾?。?/div>
    Deafness, autosomal recessive, 42 (DFNB42)
  • 亞細胞定位:
    Cell membrane; Single-pass type I membrane protein.; [Isoform 5]: Cytoplasm, cytosol.
  • 蛋白家族:
    Immunoglobulin superfamily, LISCH7 family
  • 組織特異性:
    Mainly expressed in prostate and to a lower extent in testis, pancreas, kidney, heart and liver.
  • 數據庫鏈接:

    HGNC: 28741

    OMIM: 609646

    KEGG: hsa:286676

    STRING: 9606.ENSP00000345667

    UniGene: Hs.98484



主站蜘蛛池模板: 少妇扒开双腿让我看个够| 真人祼交二十三式视频| 狠狠色噜噜狠狠狠狠888奇禾| 国产午夜精品一区二区三区漫画| 97久久精品人人槡人妻人| 荫道bbwbbb高潮潮喷| 中文字幕亚洲色妞精品天堂| 国产在线无码一区二区三区| 亚洲成年轻人电影网站www| 国产av一区二区三区| 高大丰满熟妇丰满的大白屁股| 日本亚洲vr欧美不卡高清专区| 99亚洲精品自拍av成人| 中文亚洲欧美日韩无线码| 中文字幕丰满孑伦无码精品| 亚洲日韩欧美国产另类综合| 免费国产在线精品一区二区三区| 亚洲人成人无码网www电影首页| 日日躁夜夜躁狠狠久久av| 天天爽夜夜爽人人爽一区二区| 日韩激情无码免费毛片| 免费无码成人av电影在线播放 | 国产乱人伦偷精品视频免观看| 天天槽夜夜槽槽不停| 先锋影音男人av资源| 国产亚洲精品美女久久久久| 狠狠色噜噜狠狠狠狠888奇禾| 国产公开久久人人97超碰| 成人性生交大片免费卡看| 亚洲国产精品久久人人爱| 中文字幕日产熟女乱码| 六月丁香亚洲综合在线视频 | 欧美人与禽zozzo性伦交| 男女18禁啪啪无遮挡激烈网站| 麻豆国产人妻欲求不满谁演的| 国产免费啪嗒啪嗒视频看看| 国模小黎自慰337p人体| 免费又黄又爽又色的视频| 亚洲成在人线免费观看| 国内精品乱码卡一卡2卡| 日本中文字幕亚洲乱码|