Anti-IPO9 Polyclonal Antibody-一抗-抗体-蛋白与免疫

Anti-IPO9 Polyclonal Antibody

品牌:solarbio | 货号:K007739P

英文名称 Anti-IPO9 Polyclonal Antibody
宿主 Rabbit
别名 Imp9
应用 WB IHC
稀释比例 WB 1:200-1000. IHC 1:50-200.
交叉反应 Human Mouse
蛋白分子量 116kDa
Gene ID 55705
保存 Store at -20°C. Avoid freeze / thaw cycles.
储存液 Buffer: PBS with 0.03% Proclin300, 50% glycerol, pH7.3.
纯化方法 Affinity purification
亚型 IgG
免疫原 A synthetic peptide of human IPO9
性状 液体
Public Immunogen Range A synthetic peptide of human IPO9
Subcellular Locations Cytoplasm
Swiss Prot Q96P70
克隆类型 Polyclonal Antibody
背景资料 Importin-9, also known as Imp9 or IPO9, is a 1,041 amino acid protein that contains one importin N-terminal domain and belongs to the Importin-∫ family. Localized to both the nucleus and the cytoplasm, Importin-9 functions as a nuclear transport receptor that mediates the docking of the Importin complex to the nuclear pore complex (NPC). Importin-9 mediates nuclear import of H2B histone, Ribosomal Protein S7 and Ribosomal Protein L18A. The gene encoding Importin-9 is located on human chromosome 1, the largest human chromosome that spans about 260 million base pairs and makes up 8% of the human genome.

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货号:USP6301
包装:100mL
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USP Solution Zinc Sulfate 0.0500 Molar Conforms to USP 34 品牌b>:Reagecon;订货号b>:USP6301 类别:b>美国药典标准溶液

Anti-NTRK1 Polyclonal Antibody-一抗-抗体-蛋白与免疫

Anti-NTRK1 Polyclonal Antibody

品牌:solarbio | 货号:K007565P

英文名称 Anti-NTRK1 Polyclonal Antibody
宿主 Rabbit
别名 MTC;TRK;TRK1;TRKA;Trk-A;p140-TrkA
应用 IHC
稀释比例 IHC 1:100-300.
交叉反应 Human Mouse Rat
蛋白分子量 87/84/77kDa
Gene ID 4914
保存 Store at -20°C. Avoid freeze / thaw cycles.
储存液 Buffer: PBS with 0.03% Proclin300, 50% glycerol, pH7.3.
纯化方法 Affinity purification
亚型 IgG
免疫原 A synthetic peptide of human NTRK1
性状 液体
Public Immunogen Range A synthetic peptide of human NTRK1
Subcellular Locations Cytoplasm
Swiss Prot P04629
克隆类型 Polyclonal Antibody
背景资料 This gene encodes a member of the neurotrophic tyrosine kinase receptor (NTKR) family. This kinase is a membrane-bound receptor that, upon neurotrophin binding, phosphorylates itself and members of the MAPK pathway. The presence of this kinase leads to cell differentiation and may play a role in specifying sensory neuron subtypes. Mutations in this gene have been associated with congenital insensitivity to pain, anhidrosis, self-mutilating behavior, mental retardation and cancer. Alternate transcriptional splice variants of this gene have been found, but only three have been characterized to date.