欧美日韩国产一区高清_亚洲综合日韩免费av_在线黄色视频不卡_美女高潮喷水免费网站_亚洲AV日韩AV蜜桃在线播放_色99久久综合网_干人妻潮喷无码视频_天天看片高清观看免费_国模性爱无码视频_在线亚洲精品国产二区图片欧美

最近搜索:細胞培養(yǎng) 微生物學 分子生物 生物化學
首頁>>免疫學>>一抗>>細胞纖毛內轉運同源蛋白46抗體
細胞纖毛內轉運同源蛋白46抗體
  • 產品貨號:
    BN40465R
  • 中文名稱:
    細胞纖毛內轉運同源蛋白46抗體
  • 英文名稱:
    Rabbit anti-IFT46 Polyclonal antibody
  • 品牌:
    Biorigin
  • 貨號

    產品規(guī)格

    售價

    備注

  • BN40465R-100ul

    100ul

    ¥2360.00

    交叉反應:Human 推薦應用:WB,IHC-P,IHC-F,ICC,IF,ELISA

  • BN40465R-200ul

    200ul

    ¥3490.00

    交叉反應:Human 推薦應用:WB,IHC-P,IHC-F,ICC,IF,ELISA

產品描述

英文名稱IFT46
中文名稱細胞纖毛內轉運同源蛋白46抗體
別    名C11orf2; C11orf60; IFT46; IFT46_HUMAN; Intraflagellar transport protein 46 homolog.  
研究領域細胞生物  信號轉導  細胞骨架  
抗體來源Rabbit
克隆類型Polyclonal
交叉反應Human, 
產品應用WB=1:500-2000 ELISA=1:5000-10000 IHC-P=1:100-500 IHC-F=1:100-500 ICC=1:100-500 IF=1:100-500 (石蠟切片需做抗原修復)
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
分 子 量34kDa
細胞定位細胞漿 
性    狀Liquid
濃    度1mg/ml
免 疫 原KLH conjugated synthetic peptide derived from human IFT46:101-200/304 
亞    型IgG
純化方法affinity purified by Protein A
儲 存 液0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
保存條件Shipped at 4℃. Store at -20 °C for one year. Avoid repeated freeze/thaw cycles.
PubMedPubMed
產品介紹IFT46 is a 304 amino acid protein that belongs to the IFT46 family. IFT46 localizes to the cilium basal body but can also be found along the length of the cilium and is a part of a complex involved in intraflagellar transport (IFT). In addition, IFT46 is involved in the bi-directional movement of particles that is required for the assembly, maintenance, and functionality of primary cilia. Furthermore, IFT46 may be involved in skeletogenesis and chondrocyte maturation. Two isoforms exist due to alternate splicing events and the gene encoding IFT46 maps to human chromosome 11. Chromosome 11 houses over 1,400 genes and comprises nearly 4% of the human genome. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are associated with defects in genes that maps to chromosome 11.

Function:
Forms part of a complex involved in intraflagellar transport (IFT), the bi-directional movement of particles required for the assembly, maintenance and functioning of primary cilia. May play a role in chondrocyte maturation and skeletogenesis (By similarity).

Subunit:
Part of the IFT complex B. Interacts with IFT57, IFT88 and DAW1 (By similarity).

Subcellular Location:
Cytoplasm, cytoskeleton, cilium basal body (By similarity). Cell projection, cilium (By similarity). Note=Expression is concentrated at the cilium basal body but is also detected along the length of the cilium (By similarity).

Similarity:
Belongs to the IFT46 family.

SWISS:
Q9NQC8

Gene ID:
56912

Database links:

Entrez Gene: 56912 Human

SwissProt: Q9NQC8 Human

Unigene: 533738 Human



Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications