CoraLite® Plus 750-conjugated MBP tag Monoclonal antibody
MBP tag Monoclonal Antibody for WB
Host / Isotype
Mouse / IgG2a
Reactivity
recombinant protein
Applications
WB
Conjugate
CoraLite® Plus 750 Fluorescent Dye
CloneNo.
4C6H4
验证数据展示
经过测试的应用
Positive WB detected in | Recombinant protein |
For other applications, we recommend the unconjugated version of this antibody, 66003-1-Ig
推荐稀释比
Application | Dilution |
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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
CL750-66003 targets MBP tag in WB applications and shows reactivity with recombinant protein samples.
Tested Applications | WB Application Description |
Tested Reactivity | recombinant protein |
Immunogen | MBP tag fusion protein Ag0942 种属同源性预测 |
Host / Isotype | Mouse / IgG2a |
Class | Monoclonal |
Type | Antibody |
Full Name | MBP tag |
Synonyms | |
Calculated Molecular Weight | 40 kDa |
Observed Molecular Weight | 40 kDa |
Gene Symbol | |
Gene ID (NCBI) | |
Conjugate | CoraLite® Plus 750 Fluorescent Dye |
Excitation/Emission Maxima Wavelengths | 755 nm / 780 nm |
Form | Liquid |
Purification Method | Protein A purification |
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
Protein tags are protein or peptide sequences located either on the C- or N- terminal of the target protein, which facilitates one or several of the following characteristics: solubility, detection, purification, localization and expression. Maltose binding protein(MBP) is the 370 amino acid product of the E.coli mal E gene. MBP is a useful affinity tag that can increase the expression level and solubility of the resulting tagged protein. The MBP tag also promotes proper folding of the attached protein. Plasmid vectors have been constructed utilizing the MBP domain that allow the synthesis of high levels of MBP-fusion proteins that can be purified in a one step procedure by affinity chromatography cross linked amylose resin. Once bound to amylose, the MBP protein can then be separated from the target protein by cleavage by coagulation Factor Xa at a specific four residue site. Alternatively, the intact fusion protein can be specifically eluted from the resin by the addition of excess free maltose. Subsequent to elution, MBP fusion protein can be visualized either by Western blot analysis or immunoprecipitation using antibodies specific for the MBP-tag. An antibody to MBP can also be used to isolate or detect expression of the protein.
实验方案
Product Specific Protocols | |
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WB protocol for CL Plus 750 MBP tag antibody CL750-66003 | Download protocol |
Standard Protocols | |
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Click here to view our Standard Protocols |