PEX12 抗体 (AA 290-359)
This anti-PEX12 antibody is a 兔 多克隆 antibody detecting PEX12 in WB. Suitable for 人.
1 image
Quick Overview for PEX12 抗体 (AA 290-359) (ABIN7269246)
抗原
See all PEX12 抗体
PEX12
(Peroxisomal Biogenesis Factor 12 (PEX12))
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)
-
-
抗原表位
- AA 290-359
-
原理
- PEX12 Rabbit pAb
-
序列
- YNSDSPLLPK MKTVCPLCRK TRVNDTVLAT SGYVFCYRCV FHYVRSHQAC PITGYPTEVQ HLIKLYSPEN
-
交叉反应
- 人
-
产品特性
- Polyclonal Antibodies
-
纯化方法
- Affinity purification
-
免疫原
- Recombinant fusion protein containing a sequence corresponding to amino acids 290-359 of human PEX12 (NP_000277.1).
-
亚型
- IgG
-
-
anti-Peroxisomal Biogenesis Factor 12 (PEX12) (Internal Region) antibody
PEX12 适用: 人, 小鼠, 大鼠 WB, ELISA, ICC, IF, IHC 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
-
-
应用备注
- WB,1:500 - 1:2000
-
限制
- 仅限研究用
-
-
-
状态
- Liquid
-
缓冲液
- PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.
-
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. Avoid freeze / thaw cycles.
-
-
- PEX12 (Peroxisomal Biogenesis Factor 12 (PEX12))
-
别名
- PEX12
-
背景
- 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).,PEX12,PAF-3,PBD3A,Signal Transduction,PEX12
-
分子量
- 40kDa
-
基因ID
- 5193
-
UniProt
- O00623
抗原
-
You are here:
