GEMIN4 抗体 (AA 251-350) (Biotin)
-
- 抗原 See all GEMIN4 抗体
- GEMIN4 (Gem (Nuclear Organelle) Associated Protein 4 (GEMIN4))
-
抗原表位
- AA 251-350
-
适用
- 人
-
宿主
- 兔
-
克隆类型
- 多克隆
-
标记
- This GEMIN4 antibody is conjugated to Biotin
-
应用范围
- Western Blotting (WB), ELISA, Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunohistochemistry (Frozen Sections) (IHC (fro))
- 交叉反应
- 人
- 预测反应
- Mouse,Rat,Dog,Rabbit
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human Gemin 4
- 亚型
- IgG
- Top Product
- Discover our top product GEMIN4 Primary Antibody
-
-
- 应用备注
-
WB 1:300-5000
IHC-P 1:200-400
IHC-F 1:100-500 - 限制
- 仅限研究用
-
- 状态
- Liquid
- 浓度
- 1 μg/μL
- 缓冲液
- Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.
- 储存液
- ProClin
- 注意事项
- This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
- 储存条件
- -20 °C
- 储存方法
- Store at -20°C for 12 months.
- 有效期
- 12 months
-
- 抗原
- GEMIN4 (Gem (Nuclear Organelle) Associated Protein 4 (GEMIN4))
- 别名
- Gemin 4 (GEMIN4 产品)
- 别名
- HC56 antibody, HCAP1 antibody, HHRF-1 antibody, p97 antibody, 4932415L08Rik antibody, AU015359 antibody, im:7143815 antibody, wu:fc41c09 antibody, zgc:110169 antibody, GEMIN4 antibody, RGD1563715 antibody, gem nuclear organelle associated protein 4 antibody, gem (nuclear organelle) associated protein 4 antibody, GEMIN4 antibody, Gemin4 antibody, gemin4 antibody
- 背景
-
Synonyms: Gemin4, Gemin-4, Component of gems 4, Gem associated protein 4, HC56, HHRF 1, GEMI4_HUMAN.
Background: Gemin4 is a component of the SMN core complex which, while in the cytoplasm, plays an essential role in ribonucleoprotein (snRNP) assembly, including the biogenesis, delivery and recycling of snRNPs to the spliceosome. In the nucleus, where SMN is required for pre-mRNA splicing, Gemin4 concentrates next to coiled bodies in subnuclear structures called gems, that are highly enriched in splicosomal snRNPs, and in the nucleolus. Deletion or loss-of-function mutations in the SMN lead to the neurodegenerative disease spinal muscular atrophy (SMA). The human Gemin4 maps to chromosome 17p13.
- 基因ID
- 50628
- 途径
- Ribonucleoprotein Complex Subunit Organization
-