PEX12 抗体 (AA 180-260)
Our Local Distributor
北京 101111
Quick Overview for PEX12 抗体 (AA 180-260) (ABIN8123668)
抗原
See all PEX12 抗体适用
宿主
克隆类型
标记
应用范围
-
-
抗原表位
- AA 180-260
-
原理
- PEX12 Antibody
-
特异性
- PEX12 Polyclonal Antibody detects endogenous levels of protein.
-
纯化方法
- The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
-
免疫原
- Synthesized peptide derived from human protein . at AA range: 180-260
-
亚型
- IgG
-
-
anti-Peroxisomal Biogenesis Factor 12 (PEX12) (Internal Region) antibody
PEX12 适用: 人, 小鼠, 大鼠 WB, ICC, IF, IHC 宿主: 兔 Polyclonal unconjugated
anti-Peroxisomal Biogenesis Factor 12 (PEX12) (AA 131-158) antibodyPEX12 适用: 人 WB 宿主: 兔 Polyclonal RB22647 unconjugated
anti-Peroxisomal Biogenesis Factor 12 (PEX12) (AA 290-359) antibodyPEX12 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
anti-Peroxisomal Biogenesis Factor 12 (PEX12) (AA 1-359) antibodyPEX12 适用: 人 ELISA, WB 宿主: 小鼠 Polyclonal unconjugated
-
-
应用备注
- WB 1:500-2000 ELISA 1:5000-20000
-
限制
- 仅限研究用
-
-
-
状态
- Liquid
-
缓冲液
- Liquid in PBS containing 50 % glycerol, and 0.02 % 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
- -20 °C
-
储存方法
- Store at -20°C/1 year
-
有效期
- 12 months
-
-
- PEX12 (Peroxisomal Biogenesis Factor 12 (PEX12))
-
别名
- PEX12
-
背景
-
Background: peroxisomal biogenesis factor 12(PEX12) Homo sapiens This gene belongs to the peroxin-12 family. 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. Defects in this gene are a cause of Zellweger syndrome (ZWS). [provided by RefSeq, Oct 2008],
Gene Name: PEX12 PAF3
Protein Name: Peroxisome assembly protein 12 (Peroxin-12) (Peroxisome assembly factor 3) (PAF-3)
-
基因ID
- 5193
-
UniProt
- O00623
抗原
-
