76 Results for "

phloem mobility

" in MedChemExpress (MCE) Product Catalog:
Products (76)

76 Results for "phloem mobility" in MCE Product Catalog:

8
8 Publications Verification
Cat. No.: HY-P70570
Purity:  ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: HMGB1; Sulfoglucuronyl Carbohydrate Binding Protein; Prev. HMG1; Amphoterin; High mobility Group Protein B1; HMG-1; High mobility Group Protein 1; Nuclear Dot-Associated Sp100 Protein; SBP-1; Nuclear Autoantigen Sp-100; HMG3; High-mobility Group Box 1; Hi
Species:  
Human
Source:  
E. coli
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5
5 Cited Publications
Cat. No.: HY-P73104
Purity:  ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: HMGB1; Sulfoglucuronyl Carbohydrate Binding Protein; Prev. HMG1; Amphoterin; High mobility Group Protein B1; HMG-1; High mobility Group Protein 1; Nuclear Dot-Associated Sp100 Protein; SBP-1; Nuclear Autoantigen Sp-100; HMG3; High-mobility Group Box 1; Hi
Species:  
Mouse
Source:  
HEK293
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5
5 Cited Publications
Cat. No.: HY-P73104A
Purity:  ≥ 80%, as determined by reducing SDS-PAGE.
Synonyms: HMGB1; Sulfoglucuronyl Carbohydrate Binding Protein; Prev. HMG1; Amphoterin; High mobility Group Protein B1; HMG-1; High mobility Group Protein 1; Nuclear Dot-Associated Sp100 Protein; SBP-1; Nuclear Autoantigen Sp-100; HMG3; High-mobility Group Box 1; Hi
Species:  
Mouse
Source:  
HEK293
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3
3 Cited Publications
Cat. No.: HY-P80183
Synonyms: HMG1, HMGB1, High mobility group protein B1, High mobility group protein 1, HMG-1

Host:  

Rabbit

Application:  

WB, ICC/IF, IHC-P, FC

Reactivity:  

Human, Mouse, Rat

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3
3 Cited Publications
Cat. No.: HY-P70274
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: HMGB1; Sulfoglucuronyl Carbohydrate Binding Protein; Prev. HMG1; Amphoterin; High mobility Group Protein B1; HMG-1; High mobility Group Protein 1; Nuclear Dot-Associated Sp100 Protein; SBP-1; Nuclear Autoantigen Sp-100; HMG3; High-mobility Group Box 1; Hi
Species:  
Human
Source:  
HEK293
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2
2 Cited Publications
Cat. No.: HY-14307
CAS No.: 1247028-61-0
Purity:  98.84%
Necrocide 1, a necrosis by sodium overload (NECSO) inducer, is a selective transient receptor potential melastatin 4 (TRPM4) agonist with an EC50 of 306.3 nM for human TRPM4. Necrocide 1 triggers TRPM4-dependent necrotic cell death through the induction of sodium influx. Necrocide 1 induces hallmarks of immunogenic cell death incurring calreticulin (CALR) exposure, ATP secretion and high mobility group box 1 (HMGB1) release. Necrocide 1 can be used for the study of breast and prostate cancer .
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2
2 Cited Publications
Cat. No.: HY-124750
CAS No.: 1120332-55-9
Purity:  99.69%
NecroX-7 is a potent free radical scavenger and a HMGB1 (high-mobility group box 1) inhibitor. NecroX-7 can be used as an antidote to acetaminophen toxicity. NecroX-7 exerts a protective effect by preventing the release of HMGB1 in ischemia/reperfusion injury. NecroX-7 inhibits the HMGB1-induced release of TNF and IL-6, as well as the expression of TLR-4 and receptor for advanced glycation end products. NecroX-7 can be used graft-versus-host disease (GVHD) research .
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2
2 Cited Publications
Cat. No.: HY-P70332
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: HMGB2; High mobility Group Protein 2; Prev. HMG2; HMG-2; High mobility Group Protein B2; High-mobility Group Box 2; High mobility Group Box 2; High-mobility Group (Nonhistone Chromosomal) Protein 2
Species:  
Human
Source:  
HEK293
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2
2 Cited Publications
Cat. No.: HY-P72797
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: HMGB1; Sulfoglucuronyl Carbohydrate Binding Protein; Prev. HMG1; Amphoterin; High mobility Group Protein B1; HMG-1; High mobility Group Protein 1; Nuclear Dot-Associated Sp100 Protein; SBP-1; Nuclear Autoantigen Sp-100; HMG3; High-mobility Group Box 1; Hi
Species:  
Human
Source:  
E. coli
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2
2 Cited Publications
Cat. No.: HY-P73102
Purity:  ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: HMGB1; Sulfoglucuronyl Carbohydrate Binding Protein; Prev. HMG1; Amphoterin; High mobility Group Protein B1; HMG-1; High mobility Group Protein 1; Nuclear Dot-Associated Sp100 Protein; SBP-1; Nuclear Autoantigen Sp-100; HMG3; High-mobility Group Box 1; Hi
Species:  
Human
Source:  
HEK293
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2
2 Cited Publications
Cat. No.: HY-P700182AF
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: HMGB1; Sulfoglucuronyl Carbohydrate Binding Protein; Prev. HMG1; Amphoterin; High mobility Group Protein B1; HMG-1; High mobility Group Protein 1; Nuclear Dot-Associated Sp100 Protein; SBP-1; Nuclear Autoantigen Sp-100; HMG3; High-mobility Group Box 1; Hi
Species:  
Mouse
Source:  
E. coli
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1
1 Cited Publications
Cat. No.: HY-P79315
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: HMGN1; Non-Histone Chromosomal Protein HMG-14; Prev. HMG14; MGC104230; High mobility Group Nucleosome-Binding Domain-Containing Protein 1; MGC117425; High-mobility Group (Nonhistone Chromosomal) Protein 14; FLJ27265; High-mobility Group Nucleosome Binding
Species:  
Human
Source:  
E. coli
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Cat. No.: HY-107869
CAS No.: 476-34-6
Purity:  99.12%
Target:  

Fluorescent Dye

Research Areas:  

Cancer

Isoindigo acts as the acceptor unit in donor-acceptor (D-A) conjugated polymers and belongs to the indigo dye family. Isoindigo contains two lactam rings and exhibits strong electron-withdrawing properties. Isoindigo can be used in dyeing and pigment preparation. Isoindigo shows high mobility and excellent environmental stability in field-effect transistors (FETs). Isoindigo possesses the activity to inhibit tumor cell proliferation and has certain anti-tumor activity .
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Cat. No.: HY-N2055
CAS No.: 19895-95-5
Kaempferol 3-O-sophoroside is an orally active derivative of Kaempferol. It exhibits anti-inflammatory, analgesic, and antidepressant effects. Kaempferol 3-O-sophoroside is an inhibitor of the cell surface receptor toll-like receptor (TLR) 2/4 for High mobility group box 1 (HMGB1), and it also exerts anti-inflammatory effects by blocking the activation of NF-κB expression and the production of TNF-α. Kaempferol 3-O-sophoroside promotes the production of brain-derived neurotrophic factor (BDNF) and enhances autophagy by binding to AMP-activated protein kinase (AMPK), thereby exerting antidepressant effects. Kaempferol 3-O-sophoroside holds promise for research in the fields of inflammation and neurodegenerative diseases .
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Cat. No.: HY-N3097
CAS No.: 18836-52-7
Pellitorine is a bioactive natural amide compound. Pellitorine can competitively antagonize the activation of TRPV1 by Capsaicin (HY-10448), thereby reducing pain signal transmission. Pellitorine improves cognitive dysfunction by upregulating the BDNF-ERK1/2-CREB and Nrf2-HO-1 pathways. Pellitorine exerts anti-inflammatory and anti-sepsis effects by inhibiting the release of high mobility group protein B1 (HMGB1) and the expression of RAGE/TLR4. Pellitorine exerts its antithrombotic effect by prolonging the clotting time, inhibiting the activity of clotting factors and thrombin. Pellitorine inhibits lipid peroxidation and resists ferroptosis by upregulating GPX4 and DHODH. Pellitorine kills Aedes aegypti mosquito larvae by inhibiting V-type H⁺-ATPase and aquaporin 4 (AaAQP4). Pellitorine exhibits anti-cancer activity (e.g., leukemia and breast cancer) and has inhibitory effects on certain bacteria .
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Cat. No.: HY-101532
CAS No.: 98169-85-8
Purity:  ≥98.0%
Synonyms: β-CDN3; 6A-deoxy-6A-azido-β-cyclodextrin
Research Areas:  

Others

6A-Azido-6A-deoxy-β-cyclodextrin (β-CDN3) is a site-specifically modified β-cyclodextrin with a single azido group replacing the hydroxyl group at the C6 position. 6A-Azido-6A-deoxy-β-cyclodextrin forms a host-guest inclusion complex with Dexamethasone (HY-14648), localizing the drug within its hydrophobic cavity, which restricts the rotational mobility of the drug and places Dexamethasone in a less polar environment. 6A-Azido-6A-deoxy-β-cyclodextrin acts as a coupling agent to graft β-cyclodextrin onto thermosensitive nanogels via strain-promoted alkyne-azide cycloaddition (SPAAC). 6A-Azido-6A-deoxy-β-cyclodextrin also serves as a click chemistry reagent. It contains an azide group and undergoes copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules bearing an alkyne group. It also undergoes strain-driven alkyne-azide cycloaddition (SPAAC) with molecules containing DBCO or BCN groups .
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Cat. No.: HY-122026
CAS No.: 1962178-27-3
Purity:  98.43%
Synonyms: PF-367
Target:  

GSK-3

Research Areas:  

Neurological Disease

PF-04802367 (PF-367) is a highly selective GSK-3 inhibitor with an IC50 of 2.1 nM based on a recombinant human GSK-3β enzyme assay and 1.1 nM based on ADP-Glo assay. PF-04802367 shows desirable central nervous system (CNS) properties and potency. PF-04802367 is equally effective at inhibition of the two known GSK-3 isoforms (GSK-3α and GSK-3β) with IC50 values of 10.0 and 9.0 nM in mobility shift assays, respectively .
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Cat. No.: HY-W014386
CAS No.: 132-32-1
9-Ethyl-9H-carbazol-3-amineWith high electron mobility and other favorable electronic properties, the compound is known for its use in organic electronic devices such as organic light-emitting diodes (OLED)and organic solar cells) have been investigated for potential applications. 9-Ethyl-9H-carbazol-3-amineIt can also be used as a starting material for the synthesis of other organic compounds.
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Cat. No.: HY-D2912
Cys-shift probe-1 (compound 13) is a potent Cys-shift probe. Cys-shift probe-1 can improve the ion mobility of labeled peptides and be used in protein analysis .
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Cat. No.: HY-B1849
CAS No.: 51235-04-2
Research Areas:  

Others

Hexazinone is a triazinone herbicide with high mobility and persistence in soil. Hexazinone is mainly degraded by soil microorganisms, and its degradation and mineralization processes are significantly affected by soil texture (faster in clay loam) and application method (mixed application can improve its bioavailability and mineralization rate). Hexazinone exhibits mild to moderate acute oral toxicity and has significant eye irritation .
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