CoraLite® Plus 488-conjugated PEX19 Monoclonal antibody
PEX19 Monoclonal Antibody for IF/ICC
Host / Isotype
Mouse / IgG1
Reactivity
human, mouse, rat, pig
Applications
IF/ICC
Conjugate
CoraLite® Plus 488 Fluorescent Dye
CloneNo.
3H2C2
验证数据展示
经过测试的应用
Positive IF/ICC detected in | HeLa cells |
For other applications, we recommend the unconjugated version of this antibody, 68555-1-Ig
推荐稀释比
Application | Dilution |
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Immunofluorescence (IF)/ICC | IF/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.
Tested Applications | IF/ICC Application Description |
Tested Reactivity | human, mouse, rat, pig |
Immunogen | PEX19 fusion protein Ag6858 种属同源性预测 |
Host / Isotype | Mouse / IgG1 |
Class | Monoclonal |
Type | Antibody |
Full Name | peroxisomal biogenesis factor 19 |
Synonyms | PMPI, PMP1, PEX, Peroxin-19, OK/SW-cl.22 |
Calculated Molecular Weight | 33 kDa |
Observed Molecular Weight | 35-40 kDa |
GenBank Accession Number | BC000496 |
Gene Symbol | PEX19 |
Gene ID (NCBI) | 5824 |
Conjugate | CoraLite® Plus 488 Fluorescent Dye |
Excitation/Emission Maxima Wavelengths | 493 nm / 522 nm |
Form | Liquid |
Purification Method | Protein G purification |
UNIPROT ID | P40855 |
Storage Buffer | PBS with 50% Glycerol, 0.05% Proclin300, 0.5% BSA, pH 7.3. |
Storage Conditions | 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 | |
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IF protocol for CL Plus 488 PEX19 antibody CL488-68555 | Download protocol |
Standard Protocols | |
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Click here to view our Standard Protocols |