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FITC標記(jì)的(dí)錨蛋(dàn)白重(zhòng)復結構域蛋白(bái)20A1抗體(tǐ)
英文名(míng)稱Anti-ANKRD20A1/FITC
中(zhōng)文名稱:FITC標(biāo)記的錨蛋白重復結構(gòu)域蛋白(bái)20A1抗(kàng)體
別(bié) 名A20A1_HUMAN; ANKRD20A; ANKRD20A1; Ankyrin repeat domain 20 family member A1; Ankyrin repeat domain 20A; Ankyrin repeat domain containing protein 20A1; Ankyrin repeat domain-containing protein 20A1; DKFZp434A171.
規格:100ul
說 明 書100ul
研(yán)究領域心血(xiě)管(guǎn) 細(xì)胞生物 免疫(yì)學(xué) 神(shén)經生物學
抗體來源Rabbit
克隆(lóng)類型(xíng)Polyclonal
交叉反應 Human,
產品應(yīng)用IF=1:50-200
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
分 子 量94kDa
性(xìng) 狀Lyophilized or Liquid
濃 度1mg/ml
免(miǎn) 疫 原(yuán)KLH conjugated synthetic peptide derived from human ANKRD20A1
亞 型IgG
純(chún)化(huà)方法affinity purified by Protein A
儲(chǔ) 存 液0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
保存條件Store at -20 °C for one year. Avoid repeated freeze/thaw cycles. The lyophilized antibody is stable at room temperature for at least one month and for greater than a year when kept at -20°C. When reconstituted in sterile pH 7.4 0.01M PBS or diluent of antibody the antibody is stable for at least two weeks at 2-4 °C.
產(chǎn)品介紹background:
Ankyrins are membrane adaptor molecules that play important roles in coupling integral membrane proteins to the spectrin-based cytoskeleton network. Mutations of ankyrin genes lead to severe genetic diseases such as fatal cardiac arrhythmias and hereditary spherocytosis. ANKRD20A (ankyrin repeat domain-containing protein 20A) is an 823 amino acid protein that contains five ANK repeats. The gene encoding ANKRD20A maps to chromosome 9, which consists of about 145 million bases and encodes nearly 900 genes. Considered to play a role in gender determination, deletion of the distal portion of 9p can lead to development of male to female sex reversal, the phenotype of a female with a male X,Y genotype. Hereditary hemorrhagic telangiectasia, which is characterized by harmful vascular defects, and familial dysautonomia are associated with chromosome 9. Also, chromosome 9 is partnered with chromosome 22 in the translocation leading to the aberrant production of BCR-ABL fusion protein often found in leukemias
中(zhōng)文名稱:FITC標(biāo)記的錨蛋白重復結構(gòu)域蛋白(bái)20A1抗(kàng)體
別(bié) 名A20A1_HUMAN; ANKRD20A; ANKRD20A1; Ankyrin repeat domain 20 family member A1; Ankyrin repeat domain 20A; Ankyrin repeat domain containing protein 20A1; Ankyrin repeat domain-containing protein 20A1; DKFZp434A171.
詳細(xì)介紹：
規格:100ul
說 明 書100ul
研(yán)究領域心血(xiě)管(guǎn) 細(xì)胞生物 免疫(yì)學(xué) 神(shén)經生物學
抗體來源Rabbit
克隆(lóng)類型(xíng)Polyclonal
交叉反應 Human,
產品應(yīng)用IF=1:50-200
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
分 子 量94kDa
性(xìng) 狀Lyophilized or Liquid
濃 度1mg/ml
免(miǎn) 疫 原(yuán)KLH conjugated synthetic peptide derived from human ANKRD20A1
亞 型IgG
純(chún)化(huà)方法affinity purified by Protein A
儲(chǔ) 存 液0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
保存條件Store at -20 °C for one year. Avoid repeated freeze/thaw cycles. The lyophilized antibody is stable at room temperature for at least one month and for greater than a year when kept at -20°C. When reconstituted in sterile pH 7.4 0.01M PBS or diluent of antibody the antibody is stable for at least two weeks at 2-4 °C.
相關資料(liào)：
產(chǎn)品介紹background:
Ankyrins are membrane adaptor molecules that play important roles in coupling integral membrane proteins to the spectrin-based cytoskeleton network. Mutations of ankyrin genes lead to severe genetic diseases such as fatal cardiac arrhythmias and hereditary spherocytosis. ANKRD20A (ankyrin repeat domain-containing protein 20A) is an 823 amino acid protein that contains five ANK repeats. The gene encoding ANKRD20A maps to chromosome 9, which consists of about 145 million bases and encodes nearly 900 genes. Considered to play a role in gender determination, deletion of the distal portion of 9p can lead to development of male to female sex reversal, the phenotype of a female with a male X,Y genotype. Hereditary hemorrhagic telangiectasia, which is characterized by harmful vascular defects, and familial dysautonomia are associated with chromosome 9. Also, chromosome 9 is partnered with chromosome 22 in the translocation leading to the aberrant production of BCR-ABL fusion protein often found in leukemias
- 上(shàng)一條：FITC標記的錨(máo)蛋白重復結(jié)構域蛋白(bái)13B抗(kàng)體(tǐ)
- 下(xià)一(yī)條(tiáo)：FITC標記的錨(máo)蛋白(bái)重復(fù)結(jié)構域蛋白(bái)20A3抗(kàng)體
