PDPH(3-(2-吡啶基二硫基)丙酰肼)
PDPH(3-(2-吡啶基二硫基)丙酰肼)
Thermo Scientific™

PDPH(3-(2-吡啶基二硫基)丙酰肼)

Thermo Scientific Pierce PDPH is a short, pyridyldithiol-and-hydrazide crosslinker for reversibly conjugating sulfhydryls (cysteines) to carbonyls (aldehyde or ketones, such了解更多信息
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货号数量
22301Promo Image50 mg
货号 22301
价格(CNY)
3,231.00
飞享价
Ends: 31-Dec-2025
4,124.00
共减 893.00 (22%)
Each
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下单后预计有货日期 29-Dec-2025
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数量:
50 mg
物流信息
常规产品: 发货后, 北上广深及省会城市通常为 1-2天,二线城市通常 2-3天,三线以及偏远地区通常 4天,周末以及节假日顺延。
空运受限产品: 发货后, 北上广深及省会城市通常为 2-4天,二线城市 通常3-5天,三线以及偏远地区通常 6-10天,周末以及节假日顺延。
现货中心: 此类产品将由您身边的现货中心极速配送。
价格(CNY)
3,231.00
飞享价
Ends: 31-Dec-2025
4,124.00
共减 893.00 (22%)
Each
添加至购物车
Thermo Scientific Pierce PDPH is a short, pyridyldithiol-and-hydrazide crosslinker for reversibly conjugating sulfhydryls (cysteines) to carbonyls (aldehyde or ketones, such as those formed by oxidation of glycoprotein carbohydrates).

Features of PDPH :

Reactive groups: pyridyldisulfide and hydrazide
Reactive toward: sulfhydryl groups and carbonyl (aldehyde) groups
• Short (9.2A), sulfhydryl-to-aldehyde crosslinker with disulfide bond spacer arm (cleavable)
• Pyridyldithiol group results in attachment to sulfhydryls via disulfide bond, which can be cleaved with DTT, TCEP or other reducing agents
• Hydrazide group conjugates to oxidized sugars of glycoproteins and carbohydrates
• Use sodium meta-periodate to oxidize glycosylation (e.g., sialic acid) to reactive aldehyde groups
• Use with EDC to conjugate primary amine of hydrazide group to carboxyl groups

Product References:
Crosslinker Application Guide -- search for recent literature references for this product
仅供科研使用。不可用于诊断程序。
规格
细胞渗透性
描述PDPH
形式粉末
标记方法化学标记
分子量229.32
聚乙二醇化
产品线Pierce™
数量50 mg
反应一部分酰肼、吡啶二硫化物
运输条件环境
溶解度DMF、DMSO
间隔臂长9.2 Å
水溶性
化学反应性碳水化合物-巯基
可裂解用硫醇
交联剂类型异型双功能团试剂
产品规格标准
产品类型交联剂
间隔子短 (<10 Å)
Unit SizeEach
内容与储存
接收后,请在 4°C 下干燥储存。

常见问题解答 (FAQ)

Can you provide the shelf-life for PDPH (3-(2-pyridyldithio)propionyl hydrazide)?

PDPH (3-(2-pyridyldithio)propionyl hydrazide) is covered under our general 1-year warranty and is guaranteed to be fully functional for 12 months from the date of shipment, if stored as recommended. Please see section 8.1 of our Terms & Conditions of Sale (https://www.thermofisher.com/content/dam/LifeTech/Documents/PDFs/Terms-and-Conditions-of-Sale.pdf) for more details.

Find additional tips, troubleshooting help, and resources within our Protein Purification and Isolation Support Center.

We are using EDC to crosslink a protein onto carboxyl-modified beads. We would like to add in a linker molecule to extend the radius of beads to increase the surface area so more proteins can be immobilized. Is this possible?

To provide a linker between the beads and the target protein, you would need a molecule with a primary amine (to conjugate to the carboxyl group on the beads with EDC) on one end and another reactive group on the other (to conjugate to the protein). For instance, sulfo-SMCC (Cat. No. A39268) could be used in conjunction with PDPH (Cat. No. 22301):
The method is outlined below:
1. Conjugate the target protein to the NHS ester (amine-reactive) group of Sulfo-SMCC. This will produce a maleimide-activated target protein via its primary amines (lysines and N-terminus).
2. Remove the excess sulfo-SMCC by desalting or dialysis.
3. React the maleimide-activated target protein to PDPH via sulfhydryls. (Lysines and N-terminus now are connected to hydrazide (amine) group with an extended linker)
4. Remove excess PDPH by desalting or dialysis.
5. React the hydrazide-activated target protein with carboxyl beads in the presence of EDC.
6. Use appropriate buffer to rinse off excess target protein from the carboxyl beads.

Find additional tips, troubleshooting help, and resources within our Protein Purification and Isolation Support Center.

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证书

批号Certificate TypeDateCatalog Number(s)
3230828Certificate of Analysis2025年8月14日22301
3212982Certificate of Analysis2025年5月16日22301
YK379404Certificate of Analysis2024年1月25日22301
YD358670Certificate of Analysis2023年5月06日22301
YA357113Certificate of Analysis2023年1月13日22301
显示 5 条结果, 在上面搜索特定证书

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Product Information

引用和文献 (3)

引用和文献
Abstract
Systemic administration of a nerve growth factor conjugate reverses age-related cognitive dysfunction and prevents cholinergic neuron atrophy.
Authors:Bäckman C, Rose GM, Hoffer BJ, Henry MA, Bartus RT, Friden P, Granholm AC
Journal:J Neurosci
PubMed ID:8757256
'Intraventricular administration of nerve growth factor (NGF) in rats has been shown to reduce age-related atrophy of central cholinergic neurons and the accompanying memory impairment. Intraventricular administration of NGF is necessary because NGF will not cross the blood-brain barrier (BBB). Here we have used a novel carrier system, consisting of ... More
Conjugation of folate via gelonin carbohydrate residues retains ribosomal-inactivating properties of the toxin and permits targeting to folate receptor positive cells.
Authors:Atkinson SF, Bettinger T, Seymour LW, Behr JP, Ward CM
Journal:J Biol Chem
PubMed ID:11359781
Conjugation of folate to proteins permits receptor-mediated endocytosis via the folate receptor (FR) and delivery of the conjugate into the cytoplasm of cells. Since many cancers up-regulate the FR it has enabled the targeting of toxins to tumor cells resulting in specific cell death. However, current conjugation methods rely on ... More
Site-specific modifications of light chain glycosylated antilymphoma (LL2) and anti-carcinoembryonic antigen (hImmu-14-N) antibody divalent f1agments.
Authors:Govindan SV, Goldenberg DM, Griffiths GL, Leung SO, Losman MJ, Hansen HJ
Journal:Cancer Res
PubMed ID:7493334
Site-specific introduction of metal-chelating groups into F(ab')2 fragments of an antilymphoma antibody (LL2) possessing a natural Asn-linked light chain carbohydrate and an anti-carcinoembryonic antigen antibody (hImmu-14-N) grafted with a light chain carbohydrate site is described. For this purpose, four yttrium- (and indium)-chelating agents were used, containing a primary amino group ... More
3 total citations

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