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- 详细信息
- 文献和实验
- 技术资料
- 英文名:
Recombinant Human P4HB/PDIA1/Protein Disulfide Isomerase
- 规格:
10ug/50ug/500ug/1mg
| 规格: | 10ug | 产品价格: | ¥760.0 |
|---|---|---|---|
| 规格: | 50ug | 产品价格: | ¥2000.0 |
| 规格: | 500ug | 产品价格: | 询价 |
| 规格: | 1mg | 产品价格: | 询价 |
Recombinant Human P4HB/PDIA1/Protein Disulfide Isomerase (CF56)
产品说明(Description)
Recombinant Human Prolyl 4-Hydroxylase Subunit Beta is produced by our Mammalian expression system and the target gene encoding Asp18-Lys505 is expressed with a 6His tag at the C-terminus.
Accession #: P07237
Known as: Protein Disulfide-Isomerase; PDI; Cellular Thyroid Hormone-Binding Protein; Prolyl 4-Hydroxylase Subunit Beta; p55; P4HB; ERBA2L; PDI; PDIA1; PO4DB
制剂(Formulation)
Supplied as a 0.2 μm filtered solution of PBS, pH 7.4.
质量控制(Quality Control)
Purity: Greater than 95% as determined by reducing SDS-PAGE.
Endotoxin: Less than 0.1 ng/ug (1 EU/ug) as determined by LAL test.
运输(Shipping)
The product is shipped on dry ice/polar packs.
Upon receipt, store it immediately at the temperature listed below.
保存(Storage)
Store at ≤-70°C, stable for 6 months after receipt.
Store at ≤-70°C, stable for 3 months under sterile conditions after opening.
Please minimize freeze-thaw cycles.
背景(Background)
Protein Disulfide-Isomerase (P4HB) is an endoplasmic reticulum lumen protein that belongs to the protein disulfide isomerase family. P4HB contains two thioredoxin domains and catalyzes the formation, breakage, and rearrangement of -S-S- bonds in proteins. P4HB is involved in hydroxylation of prolyl residues in preprocollagen. P4HB has the ability to act as a chaperone that inhibits aggregation of misfolded proteins in a concentration-dependent manner. P4HB plays a role in both the influx and efflux of S-nitrosothiol-bound nitric oxide.
电泳(SDS-PAGE)
FOR RESEARCH USE ONLY
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文献和实验Expression and Isolation of Recombinant Antibody Fragments in E. coli
Central to the rapid growth in the study and application of recombinant antibodies in recent years is the ability to reliably and cost-effectively produce large quantities of functional protein. In contrast to glycosylated whole monoclonal
Selection of Human Immunoglobulin Light Chains from a Phage-Display Library
to increased levels of L chains by cleavage of disulfide links. We anticipate that availability of recombinant human L chains that catalyze the hydrolysis of VIP will permit direct examination of their disease-causing potential, for example, by examination
Vectors and Strains for Expression
include those that increase secretion of heterologous protein by overexpressing eukaryotic protein disulfide isomerase, and those that decrease hyperglycosylation or provide human-type glycosylation. This chapter also discusses methods to create multicopy
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