LURAP1L 抗体 (AbBy Fluor® 647)
-
- 抗原 See all LURAP1L products
- LURAP1L (Leucine Rich Adaptor Protein 1-Like (LURAP1L))
- 适用
- 人, 小鼠, 大鼠
-
宿主
- 兔
-
克隆类型
- 多克隆
-
标记
- This LURAP1L antibody is conjugated to AbBy Fluor® 647
-
应用范围
- Western Blotting (WB), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
- 交叉反应
- 人, 小鼠, 大鼠
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human C9orf150
- 亚型
- IgG
-
-
- 应用备注
- IF(IHC-P) 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
- LURAP1L (Leucine Rich Adaptor Protein 1-Like (LURAP1L))
- 别名
- C9orf150 (LURAP1L 产品)
- 别名
- C9orf150 antibody, bA3L8.2 antibody, RGD1308059 antibody, 1110029A09Rik antibody, AV077978 antibody, AV175137 antibody, D4Bwg0951e antibody, WI-13707 antibody, bM350F23.1 antibody, leucine rich adaptor protein 1 like antibody, leucine rich adaptor protein 1-like antibody, LURAP1L antibody, Lurap1l antibody
- 背景
-
Synonyms: LURAP1L, bA3L8.2, FLJ38505, C9orf150, Chromosome 9 open reading frame 150, CI150_HUMAN, FLJ90271, HYST0841, MGC46502, Uncharacterized protein C9orf150.
Background: C9orf150 is a 231 amino acid protein encoded by a gene that maps to human chromosome 9p23. Chromosome 9 consists of about 145 million bases, represents 4 % of the human genome and encodes nearly 900 genes. Thought 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, is associated with the chromosome 9 gene encoding endoglin protein, ENG. Familial dysautonomia is also associated with chromosome 9 though through the gene IKBKAP. Notably, chromosome 9 encompasses the largest interferon family gene cluster. Chromosome 9 is partnered with chromosome 22 in the translocation leading to the aberrant production of BCR-ABL fusion protein often found in leukemias.
- 基因ID
- 286343
-
