CoraLite® Plus 488-conjugated Myosin Light Chain 2 Monoclonal antibody
Myosin Light Chain 2 Monoclonal Antibody for IF/ICC
Host / Isotype
Mouse / IgG1
Reactivity
human, mouse, rat, pig
Applications
IF/ICC
Conjugate
CoraLite® Plus 488 Fluorescent Dye
CloneNo.
5A1F1
验证数据展示
经过测试的应用
| Positive IF detected in | C2C12 cells |
Planning an IHC experiment? We recommend our IHCeasy MYL2 Ready-To-Use IHC Kit. MYL2 primary antibody included.
For other applications, we recommend the unconjugated version of this antibody, 60229-1-Ig
推荐稀释比
| Application | Dilution |
|---|---|
| Immunofluorescence (IF) | IF : 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
CL488-60229 targets Myosin Light Chain 2 in IF applications and shows reactivity with human, mouse, rat, pig samples.
| Tested Applications | IF/ICC Application Description |
| Tested Reactivity | human, mouse, rat, pig |
| Immunogen | Myosin Light Chain 2 fusion protein Ag1356 种属同源性预测 |
| Host / Isotype | Mouse / IgG1 |
| Class | Monoclonal |
| Type | Antibody |
| Full Name | myosin, light chain 2, regulatory, cardiac, slow |
| Synonyms | CMH10, DKFZp779C0562, MLC 2, MLC 2v, MLC2, MLC2v, MYL2, Myosin Light Chain 2, Myosin Light Chain 2/MLC-2V |
| Calculated Molecular Weight | 19 kDa |
| Observed Molecular Weight | 18 kDa |
| GenBank Accession Number | BC015821 |
| Gene Symbol | MYL2 |
| Gene ID (NCBI) | 4633 |
| RRID | AB_2883123 |
| Conjugate | CoraLite® Plus 488 Fluorescent Dye |
| Excitation/Emission Maxima Wavelengths | 493 nm / 522 nm |
| Form | Liquid |
| Purification Method | Protein G purification |
| UNIPROT ID | P10916 |
| 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
MYL2, also named as MLC-2v and MLC-2, is ventricular/cardiac muscle isoform. Defects in MYL2 are the cause of cardiomyopathy familial hypertrophic type 10 (CMH10). Defects in MYL2 are the cause of cardiomyopathy familial hypertrophic with mid-left ventricular chamber type 2 (MVC2). MYL2 has been widely used as a marker of mature ventricular cardiomyocytes.
实验方案
| Product Specific Protocols | |
|---|---|
| IF protocol for CL Plus 488 Myosin Light Chain 2 antibody CL488-60229 | Download protocol |
| Standard Protocols | |
|---|---|
| Click here to view our Standard Protocols |