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首页 代理品牌 Cube Biotech Nanodisc(纳米磷脂盘) DIBMA
PureCube DIBMA 系列产品(1)
产品简介
产品详情
产品参数
相关参数
参考文献
产品简介
PureCube DIBMA 系列产品(1)

PureCube DIBMA系列产品(1)指DIMBMA 10,HEPES、DIBMA 10,TRIS、DIBMA 12,HEPES、DIBMA 12,TRIS等产品

产品详情
With diisobutylene-maleic acid (DIBMA) you can directly extract membrane proteins from cells without an intermediate step of detergent solubilization, like with SDS that would usually interfere with the proteins function. Another advantage of DIBMA as a tool for protein solubilization is the lack of an absorbance maxima at 280 nm in comparison to SMAs, as their aromatic amino acids would usually absorb at the same spectrum and therefore interfere with protein quantification. PureCube DIBMA is lyophilized from two different buffer solutions (HEPES or TRIS) to ensure a stable pH of 7.5, which is ideal for most protein solubilizations. A good publication to read up even more details about DIBMA is Oluwole et al. 2017.

For the longest time, the science behind membrane proteins relied on detergents for both solubilization and stabilization. However, detergents such as DDM or LMNG come with their set of problems. A time-consuming screening process for the correct detergent and the constant need to add it to all buffers can be avoided. But this applies to all synthetic nanodiscs.

Figure 1 shows the amount of membrane protein of interest that was stabilized by a DIBMALP in comparison to a construct using the detergent DDM. As it can clearly be seen DDM has way fewer specific bands at the desired kDA values of around 40-60 kDa.


Fig. 1: The yield of DIBMA-based nanodiscs compared to detergent micelles (e.g. DDM detergent)

An alternative to traditional DIBMAs and their sensitivity to the presence of ions inside a buffer, are our modified DIBMAs with added Glucosamine or amino-functionalized diol. As figure 2 indicates, the increased tolerance of Ca2+ is necessary. Normally DIBMA starts to precipitate in Ca2+ holding buffers at concentrations of around 25 mM. Using DIBMA-Glycerol this tolerance increases to 50 mM. There is no precipitate visible at the bottom of the tube. In comparison, normal DIBMA shows a visible precipitate at 25 mM. In terms of Mg2+ tolerance traditional DIBMA and the Glycerol-DIBMA both show a high tolerance above 50 mM.

Fig. 2: DIBMA precipitation in relation to the ion concentration. The shown concentrations start at 5 mM and are increasing in 5 mM steps up to 50 mM.


产品参数

FEATURES

Usage

Protein solubilization

Formula Weight

12,000 g/mol

pH

7.5 in buffer

dn/dc

1.35 M-1

Solubility

> 10 % in H2O

Absorbance at 280 nm

< 0.3 (1 % solution)

Mg2+ Tolerance

Dependend on DIBMA product
Increased with less charged DIBMAs

Ca2+ Tolerance

Dependend on DIBMA product
Increased with less charged DIBMAs

相关参数

Order

number

Products

Shipment

Temperature

Storage

Temperature

18001

PureCube DIBMA 10, Screening Kit, 10x50 mg, HEPES

Ambient temperature

-20°C

18002

PureCube DIBMA 10, 1g, HEPES

Ambient temperature

-20°C

18021

PureCube DIBMA 10, 10g, HEPES

Ambient temperature

-20°C

18022

PureCube DIBMA 10, 5x10g, HEPES

Ambient temperature

-20°C

18004

PureCube DIBMA 10, Screening Kit, 10x50 mg, TRIS

Ambient temperature

-20°C

18005

PureCube DIBMA 10, 1g, TRIS

Ambient temperature

-20°C

18026

PureCube DIBMA 10, 10g, TRIS

Ambient temperature

-20°C

18027

PureCube DIBMA 10, 5x10g, TRIS

Ambient temperature

-20°C

18011

PureCube DIBMA 12, Screening Kit, 10x50 mg, HEPES

Ambient temperature

-20°C

18012

PureCube DIBMA 12, 1g, HEPES

Ambient temperature

-20°C

18031

PureCube DIBMA 12, 10g, HEPES

Ambient temperature

-20°C

18032

PureCube DIBMA 12, 5x10g, HEPES

Ambient temperature

-20°C

18014

PureCube DIBMA 12, Screening Kit, 10x50 mg, TRIS

Ambient temperature

-20°C

18015

PureCube DIBMA 12, 1g, TRIS

Ambient temperature

-20°C

18036

PureCube DIBMA 12, 10g, TRIS

Ambient temperature

-20°C

18037

PureCube DIBMA 12, 5x10g, TRIS

Ambient temperature

-20°C 


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参考文献

Hernandez L.M.R. & Levental I.

1.Biophysical Journal,Available online 14 January 2023.

Zhou R., Zhang S., Nguyen H.T., Ding H., Gaffney A., Kappes J.C.,Smith Ill A.B.S, Sodroski J.G.

bioRxiv.

Voskoboynikova, N.; Orekhov, P.; Bozdaganyan, M.; Kodde, F.; Rademacher, M.; Schowe, M.; Budke-Gieseking, A.; Brickwedde, B.; Psathaki, O.-E.; Mulkidjanian, A.Y.; Cosentino, K.; Shaitan, K.V.; Steinhoff, H.-J.

MDPI.

Voskoboynikova, N.; Margheretis E.G., Kodde F., Redemacher M., Schowe M., Budke-Gieseking A., Psathaki O-E-, Steinhoff H-J., Cosentino K.

sciencedirect.

Overduin M., Trieber C., Prosser R.S., Picard L-P., Sheff J.G.

membranes.