CoraLite® Plus 488-conjugated PEX19 Monoclonal antibody

PEX19 Monoclonal Antibody for IF/ICC
Cat No. CL488-68555

产品说明书

CloneNo. 3H2C2

宿主/亚型

Mouse / IgG1

种属反应性

human, mouse, rat, pig

应用

IF/ICC

PMPI, PMP1, PEX, Peroxin-19, OK/SW-cl.22

缓冲液配方:  PBS and Azide
PBS and Azide
偶联物:  CoraLite® Plus 488

规格: 
100 μL

¥2800/ 100 μL

浓度: 1000 μg/ml


经过测试的应用

Positive IF/ICC detected inHeLa cells
For other applications, we recommend the unconjugated version of this antibody, 68555-1-Ig

推荐稀释比

应用推荐稀释比
Immunofluorescence (IF)/ICCIF/ICC : 1:50-1:500
It is recommended that this reagent should be titrated in each testing system to obtain optimal results.
Sample-dependent, Check data in validation data gallery.

产品信息

CL488-68555 targets PEX19 in IF/ICC applications and shows reactivity with human, mouse, rat, pig samples.

经测试应用 IF/ICC Application Description
经测试反应性 human, mouse, rat, pig
免疫原 PEX19 fusion protein Ag6858 种属同源性预测
宿主/亚型 Mouse / IgG1
抗体类别 Monoclonal
产品类型 Antibody
全称 peroxisomal biogenesis factor 19
别名 PMPI, PMP1, PEX, Peroxin-19, OK/SW-cl.22
计算分子量 33 kDa
观测分子量 35-40 kDa
GenBank蛋白编号BC000496
基因名称 PEX19
Gene ID (NCBI) 5824
RRIDAB_3673025
偶联类型 CoraLite® Plus 488 Fluorescent Dye
最大激发/发射波长493 nm / 522 nm
形式 Liquid
纯化方式Protein G purification
UNIPROT IDP40855
储存缓冲液 PBS with 50% Glycerol, 0.05% Proclin300, 0.5% BSA, pH 7.3.
储存条件Store at -20°C. Avoid exposure to light. Stable for one year after shipment. Aliquoting is unnecessary for -20oC storage.

背景介绍

Peroxins (PEXs) are proteins that are essential for the assembly of functional peroxisomes. PEX19 gene is necessary for early peroxisomal biogenesis. It acts both as a cytosolic chaperone and as an import receptor for peroxisomal membrane proteins (PMPs) (PMID: 14709540). PEX19 may bind newly synthesized PMPs and facilitate their insertion into the peroxisome membrane (PMID: 107044440. The peroxisome biogenesis disorders (PBDs) are a group of genetically heterogeneous autosomal recessive, lethal diseases characterized by multiple defects in peroxisome function. Defects in this gene are a cause of Zellweger syndrome (ZWS), as well as peroxisome biogenesis disorder complementation group 14 (PBD-CG14) (PMID:20683989) (PMID:10051604).

实验方案

Product Specific Protocols
IF protocol for CL Plus 488 PEX19 antibody CL488-68555Download protocol
Standard Protocols
Click here to view our Standard Protocols
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