FOPNL 抗体 (AA 6-80) (Cy7)
-
- 抗原 See all FOPNL 抗体
- FOPNL (FGFR1OP N-Terminal Like (FOPNL))
-
抗原表位
- AA 6-80
-
适用
- 小鼠, 大鼠
-
宿主
- 兔
-
克隆类型
- 多克隆
-
标记
- This FOPNL antibody is conjugated to Cy7
-
应用范围
- Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
- 交叉反应
- 小鼠, 大鼠
- 预测反应
- Human,Dog,Cow,Sheep,Pig,Horse
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human FOPNL/C16orf63
- 亚型
- IgG
- Top Product
- Discover our top product FOPNL Primary Antibody
-
anti-FGFR1OP N-Terminal Like (FOPNL) (AA 20-100) antibody
FOPNL 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
-
- 应用备注
-
IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200 - 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. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
- 有效期
- 12 months
-
- 抗原
- FOPNL (FGFR1OP N-Terminal Like (FOPNL))
- 别名
- FOPNL/C16orf63 (FOPNL 产品)
- 别名
- C16orf63 antibody, FOR20 antibody, PHSECRG2 antibody, C14H16orf63 antibody, 0610037P05Rik antibody, FGFR1OP N-terminal like antibody, Fgfr1op N-terminal like antibody, FGFR1OP N-terminal like L homeolog antibody, FOPNL antibody, Fopnl antibody, fopnl.L antibody
- 背景
-
Synonyms: C16orf63, FGFR1OP N terminal like, FGFR1OP N-terminal-like protein, FOP-related protein of 20 kDa, Fopnl, FOPNL_HUMAN, FOR20, LisH domain containing protein C16orf63, LisH domain-containing protein FOPNL, PHSECRG2, Pluripotent embryonic stem cell related protein.
Background: C16orf63, also known as FLJ31153 or DKFZp686N1651, is a 174 amino acid protein that contains one LisH domain. The gene that encodes C16orf63 maps to human chromosome 16. Chromosome 16 encodes over 900 genes in approximately 90 million base pairs, makes up nearly 3 % of human cellular DNA and is associated with a variety of genetic disorders. The GAN gene is located on chromosome 16 and, with mutation, may lead to giant axonal neuropathy, a nervous system disorder characterized by increasing malfunction with growth. The rare disorder Rubinstein-Taybi syndrome is also associated with chromosome 16, though through the CREBBP gene which encodes a critical CREB binding protein. Signs of Rubinstein-Taybi include mental retardation and predisposition to tumor growth and white blood cell neoplasias. Crohn's disease is a gastrointestinal inflammatory condition associated with chromosome 16 through the NOD2 gene. An association with systemic lupus erythematosis and a number of other autoimmune disorders with the pericentromeric region of chromosome 16 has led to the identification of SLC5A11 as a potential autoimmune modifier. The C16orf63 gene product has been provisionally designated C16orf63 pending further characterization.
- 基因ID
- 123811
- 途径
- Maintenance of Protein Location
-
