AFG3L2 Monoclonal antibody
AFG3L2 Monoclonal Antibody for WB, ELISA
Host / Isotype
Mouse / IgG2a
Reactivity
Human, mouse, rat, pig, rabbit
Applications
WB, ELISA
Conjugate
Unconjugated
CloneNo.
1C12F3
验证数据展示
经过测试的应用
| Positive WB detected in | HeLa cells, LNCaP cells, HepG2 cells, Jurkat cells, K-562 cells, pig heart tissue, rabbit heart tissue, rat heart tissue, mouse heart tissue |
推荐稀释比
| Application | Dilution |
|---|---|
| Western Blot (WB) | WB : 1:1000-1:8000 |
| 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
68517-1-Ig targets AFG3L2 in WB, ELISA applications and shows reactivity with Human, mouse, rat, pig, rabbit samples.
| Tested Applications | WB, ELISA Application Description |
| Tested Reactivity | Human, mouse, rat, pig, rabbit |
| Immunogen | AFG3L2 fusion protein Ag7180 种属同源性预测 |
| Host / Isotype | Mouse / IgG2a |
| Class | Monoclonal |
| Type | Antibody |
| Full Name | AFG3 ATPase family gene 3-like 2 (yeast) |
| Synonyms | AFG3 like protein 2, AFG3L2, FLJ25993, Paraplegin like protein |
| Calculated Molecular Weight | 88 kDa |
| Observed Molecular Weight | 80 kDa |
| GenBank Accession Number | BC065016 |
| Gene Symbol | AFG3L2 |
| Gene ID (NCBI) | 10939 |
| Conjugate | Unconjugated |
| Form | Liquid |
| Purification Method | Protein A purification |
| UNIPROT ID | Q9Y4W6 |
| 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
AFG3L2 is the catalytic subunit of the m-AAA protease, an ATP-dependent proteolytic complex of the mitochondrial inner membrane that degrades misfolded proteins and regulates ribosome assembly(PMID:17101804). Human AFG3L2 is an 80-kDa protein encoded by a 17-exon gene and highly and selectively expressed in human cerebellar Purkinje cells(PMID:20208537) and it can exsit as a truncated 65 kDa protein(PMID:18337413). Defects in AFG3L2 are the cause of spinocerebellar ataxia type 28 (SCA28) and spastic ataxia autosomal recessive type 5 (SPAX5).
实验方案
| Product Specific Protocols | |
|---|---|
| WB protocol for AFG3L2 antibody 68517-1-Ig | Download protocol |
| Standard Protocols | |
|---|---|
| Click here to view our Standard Protocols |