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Targeted therapy! The Capetin Prize winning "Click Chemistry" can be used like this!Targeted therapy! The Nobel Prize winning "Click Chemistry" can be used like this!2025-02-06
546 Results for "
HA protein
" in MedChemExpress (MCE) Product Catalog:
Products (546)
546 Results for "HA protein" in MCE Product Catalog:
173
173 Publications Verification
Cat. No.: HY-K0201
MCE Anti-HA Magnetic Beads are used for immunoprecipitation (IP) of specific HA-tagged proteins expressed in bacterial and mammalian cells and in vitro expression systems.The 1 mL volume is defined as the base specification. All larger sizes correspond to incremental volumes of this base.
29
29 Cited Publications
Synonyms: HA-1077 Hydrochloride; AT-877 Hydrochloride
Fasudil (HA-1077; AT877) Hydrochloride is a nonspecific RhoA/ROCK inhibitor and also has inhibitory effect on protein kinases, with an Ki of 0.33 μM for ROCK1, IC50s of 0.158 μM and 4.58 μM, 12.30 μM, 1.650 μM for ROCK2 and PKA, PKC, PKG, respectively. Fasudil Hydrochloride is also a potent Ca 2+ channel antagonist and vasodilator .
29
Fasudil (HA-1077; AT877) is a nonspecific RhoA/ROCK inhibitor and also has inhibitory effect on protein kinases, with an Ki of 0.33 μM for ROCK1, IC50s of 0.158 μM and 4.58 μM, 12.30 μM, 1.650 μM for ROCK2 and PKA, PKC, PKG, respectively. Fasudil is also a potent Ca 2+ channel antagonist and vasodilator .
29
29 Cited Publications
Cat. No.: HY-10341C
CAS No.: 203911-27-7
Synonyms: HA-1077 dihydrochloride; AT-877 dihydrochloride
Fasudil (HA-1077; AT877) dihydrochloride is a nonspecific RhoA/ROCK inhibitor and also has inhibitory effect on protein kinases, with an Ki of 0.33 μM for ROCK1, IC50s of 0.158 μM and 4.58 μM, 12.30 μM, 1.650 μM for ROCK2 and PKA, PKC, PKG, respectively. Fasudil dihydrochloride is also a potent Ca 2+ channel antagonist and vasodilator .
16
16 Cited Publications
Cat. No.: HY-P0239
CAS No.: 92000-76-5
Target:
16
16 Cited Publications
Cat. No.: HY-P0239A
Target:
5
5 Cited Publications
Target:
Research Areas:
LOC14 is a potent Protein disulfide isomerase (PDI) inhibitor with EC50 and Kd values of 500 nM and 62 nM, respectively. LOC14 exhibits high stability in mouse liver microsomes and blood plasma, low intrinsic microsome clearance, and low plasma-protein binding .
LOC14 inhibits PDIA3 activity, decreases intramolecular disulfide bonds and subsequent oligomerization (maturation) of HA in lung epithelial cells .
4
4 Cited Publications
Cat. No.: HY-K0201A
MCE Anti-HA Magnetic Beads (1 μm) are used for immunoprecipitation (IP) of specific HA-tagged proteins expressed in bacterial and mammalian cells andin vitro expression systems. The 1 mL is defined as the base specification. All larger sizes correspond to incremental volumes of this base.
3
1
1 Cited Publications
Cat. No.: HY-160799
CAS No.: 2412367-83-8
Target:
Research Areas:
HA-9104 is a potent and selective inhibitor of cullin-5 neddylation via virtually targeting the V30 pocket of UBE2F. HA-9104 binds to UBE2F, reduces its protein levels, and consequently inhibits cullin-5 neddylation. HA-9104 has potent growth suppression and radiosensitizing activities via targeting the UBE2F-CRL5 axis and causing DNA damage, leading to induction of apoptosis and G2/M arrest in lung and pancreatic cancer cells .
1
1 Cited Publications
HA-100 is a potent protein kinase inhibitor, with IC50s of 4 μM, 8 μM, 12 μM and 240 μM for cGMP-dependent protein kinase (PKG), cAMP-dependent protein kinase (PKA), protein kinase C (PKC) and MLC-kinase, respectively. HA-100 also used as a ROCK inhibitor .
1
1
1
1
1
1 Cited Publications
Cat. No.: HY-P73919
Purity: ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: HRAS; C-HAs/Bas P21 protein; Prev. HRAS1; P21 protein; V-HA-Ras HArvey Rat Sarcoma Viral Oncogene Homolog; C-HA-RAS1; HArvey Rat Sarcoma Viral Oncogene Homolog; C-BAS/HAS; Transforming protein P21; H-RASIDX; GTPase HRas; C-H-RAS; P21ras; H-Ras-1; Ras Fami
Species:
Human
Source:
Sf9 insect cells
1
1 Cited Publications
Cat. No.: HY-P701114
Purity: ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: TAGLN2; Epididymis Tissue protein Li 7e; Transgelin 2; Transgelin-2; SM22-AlpHA Homolog; Epididymis Secretory Sperm Binding protein; KIAA0120; Transgelin; HA1756
Species:
Human
Source:
HEK293
1
1 Cited Publications
Cat. No.: HY-P75153A
Purity: ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: GSTA1; GTH1; Glutathione S-Transferase AlpHA 1; Glutathione S-Transferase HA Subunit 1; Glutathione S-Transferase A1; S-(Hydroxyalkyl)Glutathione Lyase A1; 13-Hydroperoxyoctadecadienoate Peroxidase; Glutathione S-Alkyltransferase A1; Androst-5-Ene-3,17-Di
Species:
Human
Source:
HEK293
Research Areas:
HA-1004 is a selective inhibitor of PKA, which can inhibit lipolysis and induce vascular relaxation. HA-1004 is also a dual inhibitor of cyclic GMP-dependent protein kinase and cyclic AMP-dependent protein, and is involved in smooth muscle, second messenger, cyclic AMP and cyclic GMP regulation mechanisms. HA-1004 is an antagonist for calcium, that can be used as a vasodilator to inhibit the contraction of rabbit aortic strips, or to antagonize ERK and tyrosine hydroxylase (TH) phosphorylation in morphine abstinence rat models .
Cat. No.: HY-P4108C
Target:
Research Areas:
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Protocols
Targeted therapy! The Capetin Prize winning "Click Chemistry" can be used like this!Targeted therapy! The Nobel Prize winning "Click Chemistry" can be used like this!A suitable model is crucial in drug screening experiments. Organs can mimic the three-dimensional functional structure of internal organs, have similar spatial organization to corresponding organs, maintain some key characteristics, and reproduce some physiological functions. They are widely used for modeling and personalized drug screening physiological functions.2025-02-06
