PPAPDC3 Polyclonal antibody
PPAPDC3 Polyclonal Antibody for WB, IP, ELISA
Host / Isotype
Rabbit / IgG
Reactivity
human, mouse, rat
Applications
WB, IP, ELISA
Conjugate
Unconjugated
验证数据展示
经过测试的应用
Positive WB detected in | mouse skeletal muscle tissue |
Positive IP detected in | mouse skeletal muscle tissue |
推荐稀释比
Application | Dilution |
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Western Blot (WB) | WB : 1:500-1:1000 |
Immunoprecipitation (IP) | IP : 0.5-4.0 ug for 1.0-3.0 mg of total protein lysate |
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. |
发表文章中的应用
WB | See 3 publications below |
产品信息
The immunogen of 20635-1-AP is PPAPDC3 Fusion Protein expressed in E. coli.
Tested Applications | WB, IP, ELISA Application Description |
Cited Applications | WB |
Tested Reactivity | human, mouse, rat |
Cited Reactivity | human |
Immunogen | PPAPDC3 fusion protein Ag14676 种属同源性预测 |
Host / Isotype | Rabbit / IgG |
Class | Polyclonal |
Type | Antibody |
Full Name | phosphatidic acid phosphatase type 2 domain containing 3 |
Synonyms | C9orf67, KIAA0515, NET39, PPAPDC3 |
Calculated Molecular Weight | 271 aa, 29 kDa |
Observed Molecular Weight | 29 kDa |
GenBank Accession Number | BC006362 |
Gene Symbol | PPAPDC3 |
Gene ID (NCBI) | 84814 |
RRID | AB_10696180 |
Conjugate | Unconjugated |
Form | Liquid |
Purification Method | Antigen affinity purification |
UNIPROT ID | Q8NBV4 |
Storage Buffer | PBS with 0.02% sodium azide and 50% glycerol pH 7.3. |
Storage Conditions | Store at -20°C. Stable for one year after shipment. Aliquoting is unnecessary for -20oC storage. |
背景介绍
实验方案
Product Specific Protocols | |
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WB protocol for PPAPDC3 antibody 20635-1-AP | Download protocol |
IP protocol for PPAPDC3 antibody 20635-1-AP | Download protocol |
Standard Protocols | |
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Click here to view our Standard Protocols |
发表文章
Species | Application | Title |
---|---|---|
Genome Biol Specific nuclear envelope transmembrane proteins can promote the location of chromosomes to and from the nuclear periphery. | ||
Cells Lamin A/C Assembly Defects in LMNA-Congenital Muscular Dystrophy Is Responsible for the Increased Severity of the Disease Compared with Emery-Dreifuss Muscular Dystrophy. | ||
Front Cell Dev Biol Nuclear envelope transmembrane proteins involved in genome organization are misregulated in myotonic dystrophy type 1 muscle |