-
- 抗原 See all PEX12 抗体
- PEX12 (Peroxisomal Biogenesis Factor 12 (PEX12))
-
抗原表位
- AA 131-158
-
适用
- 人
-
宿主
- 兔
-
克隆类型
- 多克隆
-
标记
- This PEX12 antibody is un-conjugated
-
应用范围
- Western Blotting (WB)
- 预测反应
- B, M
- 纯化方法
- This antibody is purified through a protein A column, followed by peptide affinity purification.
- 免疫原
- This PEX12 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 131-158 amino acids from the Central region of human PEX12.
- 克隆位点
- RB22647
- 亚型
- Ig Fraction
- Top Product
- Discover our top product PEX12 Primary Antibody
-
anti-Peroxisomal Biogenesis Factor 12 (PEX12) (Internal Region) antibody
PEX12 适用: 人, 小鼠, 大鼠 WB, ELISA, IF, IHC, ICC 宿主: 兔 Polyclonal unconjugated
anti-Peroxisomal Biogenesis Factor 12 (PEX12) (AA 1-359) antibodyPEX12 适用: 人 WB, ELISA 宿主: 小鼠 Polyclonal unconjugated
anti-Peroxisomal Biogenesis Factor 12 (PEX12) antibodyPEX12 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
anti-Peroxisomal Biogenesis Factor 12 (PEX12) (AA 290-359) antibodyPEX12 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
-
- 应用备注
- WB: 1:1000
- 限制
- 仅限研究用
-
- 状态
- Liquid
- 缓冲液
- Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.
- 储存液
- Sodium azide
- 注意事项
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- 储存条件
- 4 °C,-20 °C
- 储存方法
- Maintain refrigerated at 2-8 °C for up to 6 months. For long term storage store at -20 °C in small aliquots to prevent freeze-thaw cycles.
- 有效期
- 6 months
-
- 抗原
- PEX12 (Peroxisomal Biogenesis Factor 12 (PEX12))
- 别名
- PEX12 (PEX12 产品)
- 背景
- Peroxins (PEXs) are proteins that are essential for the assembly of functional peroxisomes. The peroxisome biogenesis disorders (PBDs) are a group of genetically heterogeneous autosomal recessive, lethal diseases characterized by multiple defects in peroxisome function. The peroxisomal biogenesis disorders are a heterogeneous group with at least 14 complementation groups and with more than 1 phenotype being observed in cases falling into particular complementation groups. Although the clinical features of PBD patients vary, cells from all PBD patients exhibit a defect in the import of one or more classes of peroxisomal matrix proteins into the organelle.
- 分子量
- 40797
- 基因ID
- 5193
- NCBI登录号
- NP_000277
- UniProt
- O00623
-
You are here:
