-
- 抗原 See all SHOX 抗体
- SHOX (Short Stature Homeobox (SHOX))
-
适用
- 人
-
宿主
- 兔
-
克隆类型
- 多克隆
-
标记
- This SHOX antibody is un-conjugated
- 应用范围
- Western Blotting (WB), ELISA
- 纯化方法
- Antibody is purified by peptide affinity chromatography method.
- 免疫原
- Antibody produced in rabbits immunized with a synthetic peptide corresponding a region of human SHOX.
- Top Product
- Discover our top product SHOX Primary Antibody
-
anti-Short Stature Homeobox (SHOX) (AA 1-225) antibody
SHOX 适用: 人 WB 宿主: 小鼠 Polyclonal unconjugated
anti-Short Stature Homeobox (SHOX) antibodySHOX 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
anti-Short Stature Homeobox (SHOX) (AA 4-38), (N-Term) antibodySHOX 适用: 人 WB 宿主: 兔 Polyclonal RB47882 unconjugated
anti-Short Stature Homeobox (SHOX) (N-Term) antibodySHOX 适用: 人 WB, ELISA 宿主: 兔 Polyclonal unconjugated
anti-Short Stature Homeobox (SHOX) (N-Term) antibodySHOX 适用: 人, 小鼠, 犬, 大鼠, 小鸡, Pig WB 宿主: 兔 Polyclonal unconjugated
-
- 应用备注
- SHOX antibody can be used for detection of SHOX by ELISA at 1:312500. SHOX antibody can be used for detection of SHOX by western blot at 1 μg/mL, and HRP conjugated secondary antibody should be diluted 1:50,000 - 100,000.
- 限制
- 仅限研究用
-
- 状态
- Lyophilized
- 溶解方式
- Add 50 ?L of distilled water. Final antibody concentration is 1 mg/mL.
- 浓度
- 1 mg/mL
- 缓冲液
- Antibody is lyophilized in PBS buffer with 2 % sucrose.
- 注意事项
- As with any antibody avoid repeat freeze-thaw cycles.
- 储存条件
- 4 °C/-20 °C
- 储存方法
- For short periods of storage (days) store at 4 °C. For longer periods of storage, store SHOX antibody at -20 °C.
-
- 抗原
- SHOX (Short Stature Homeobox (SHOX))
- 别名
- SHOX (SHOX 产品)
- 别名
- si:ch211-134k13.1 antibody, zgc:123182 antibody, GCFX antibody, PHOG antibody, SHOXY antibody, SS antibody, short stature homeobox antibody, shox antibody, SHOX antibody
- 背景
- This gene belongs to the paired homeobox family and is located in the pseudoautosomal region 1 (PAR1) of X and Y chromosomes. Defects in this gene are associated with idiopathic growth retardation and in the short stature phenotype of Turner syndrome patients. This gene is highly conserved across species from mammals to fish to flies.This gene belongs to the paired homeobox family and is located in the pseudoautosomal region 1 (PAR1) of X and Y chromosomes. Defects in this gene are associated with idiopathic growth retardation and in the short stature phenotype of Turner syndrome patients. This gene is highly conserved across species from mammals to fish to flies. Alternatively spliced transcript variants encoding different isoforms have been noted for this gene.
- 分子量
- 32 kDa
- 基因ID
- 6473
- NCBI登录号
- NP_000442
- UniProt
- O15266
-
You are here:
