CoraLite®594-conjugated Myosin Light Chain 2 Monoclonal antibody
Myosin Light Chain 2 Monoclonal Antibody for IF/ICC, IF-P
Host / Isotype
Mouse / IgG1
Reactivity
human, mouse, rat, pig
Applications
IF/ICC, IF-P
Conjugate
CoraLite®594 Fluorescent Dye
CloneNo.
5A1F1
验证数据展示
经过测试的应用
Positive IF-P detected in | mouse heart tissue |
Positive IF/ICC 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)-P | IF-P : 1:50-1:500 |
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
CL594-60229 targets Myosin Light Chain 2 in IF/ICC, IF-P applications and shows reactivity with human, mouse, rat, pig samples.
Tested Applications | IF/ICC, IF-P 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 | MLC 2v, MYL2, MLC-2s/v, MLC-2, MLC2 |
Calculated Molecular Weight | 19 kDa |
Observed Molecular Weight | 18 kDa |
GenBank Accession Number | BC015821 |
Gene Symbol | Myosin Light Chain 2 |
Gene ID (NCBI) | 4633 |
RRID | AB_2883447 |
Conjugate | CoraLite®594 Fluorescent Dye |
Excitation/Emission Maxima Wavelengths | 588 nm / 604 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 CL594 Myosin Light Chain 2 antibody CL594-60229 | Download protocol |
Standard Protocols | |
---|---|
Click here to view our Standard Protocols |