MBP-Tag Polyclonal antibody

MBP-Tag Polyclonal Antibody for WB, ELISA
Cat No. 15089-1-AP

产品说明书

宿主/亚型

Rabbit / IgG

种属反应性

recombinant protein

应用

WB, ELISA and More (4)

Maltose Binding Protein, MBP, MBP Tag, MBP-Tag

缓冲液配方:  PBS and Azide
PBS and Azide
偶联物:  Unconjugated
Unconjugated
规格: 

-/ -


经过测试的应用

Positive WB detected inlane1: MBP-NOL6 64kd; lane2 MBP 42kd, Recombinant protein

推荐稀释比

应用推荐稀释比
Western Blot (WB)WB : 1:1000-1:6000
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

15089-1-AP targets MBP-Tag in WB, IHC, IF, IP, CoIP, ELISA applications and shows reactivity with recombinant protein samples.

经测试应用 WB, ELISA Application Description
文献引用应用WB, IHC, IF, IP, CoIP, ELISA
经测试反应性 recombinant protein
免疫原 MBP-Tag fusion protein Ag0942 种属同源性预测
宿主/亚型 Rabbit / IgG
抗体类别 Polyclonal
产品类型 Antibody
全称 MBP-Tag
别名 Maltose Binding Protein, MBP, MBP Tag, MBP-Tag
计算分子量 40 kDa
基因名称
Gene ID (NCBI)
RRIDAB_1607774
偶联类型 Unconjugated
形式 Liquid
纯化方式Antigen affinity purification
储存缓冲液 PBS with 0.02% sodium azide and 50% glycerol , pH 7.3
储存条件Store at -20°C. 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. This antibody recognizes MBP (Maltose binding protein) TAG in some expression systems.

发表文章

SpeciesApplicationTitle

Nature

Allele-selective lowering of mutant HTT protein by HTT-LC3 linker compounds.

Authors - Zhaoyang Li
ELISA

Blood

Gamma-glutamyl carboxylase mutations differentially affect the biological function of vitamin K-dependent proteins.

Authors - Zhenyu Hao
WB

Blood

γ-Glutamyl carboxylase mutations differentially affect the biological function of vitamin K-dependent proteins.

Authors - Zhenyu Hao
WB

Sci Adv

The deubiquitinases UBP12 and UBP13 integrate with the E3 ubiquitin ligase XBAT35.2 to modulate VPS23A stability in ABA signaling.

Authors - Guangchao Liu
WB

Cell Res

Modulation of microRNA processing by mismatch repair protein MutLα.

Authors - Mao Guogen G

Proc Natl Acad Sci U S A

Polyprotein strategy for stoichiometric assembly of nitrogen fixation components for synthetic biology.

Authors - Jianguo Yang
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