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Isoforms Recommended:	HSF1

Results for "

hsf1

" in MedChemExpress (MCE) Product Catalog:

By Targets:	AMPK (1) Androgen Receptor (1) Apoptosis (7) Autophagy (1) Bacterial (2) Caspase (1) Collagen (1) DNA/RNA Synthesis (2) Drug Derivative (1) Early 2 Factor (E2F) (1) ERK (1) Eukaryotic Initiation Factor (eIF) (2) HIV (2) HSP (26) JNK (2) Keap1-Nrf2 (1) Mitochondrial Metabolism (2) Mitophagy (1) NF-κB (2) PARP (1) Proteasome (2) Reactive Oxygen Species (ROS) (1) Reference Standards (4) Small Interfering RNA (siRNA) (4) TGF-beta/Smad (1) Tyrosinase (1) YAP (1)
By Research Areas:	Cancer (21) Cardiovascular Disease (2) Infection (3) Inflammation/Immunology (6) Metabolic Disease (4) Neurological Disease (5)
Oligonucleotides:	Rat Pre-designed siRNA Sets (1) Mouse Pre-designed siRNA Sets (1) Human Pre-designed siRNA Sets (2) siRNAs (4)

Inhibitors & Agonists

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Recombinant Proteins

Antibodies

Oligonucleotides

Cat. No.	Product Name	Target	Research Areas	Chemical Structure

HY-19356

Rocaglamide 25+ Cited Publications Roc-A	NF-κB HSP Eukaryotic Initiation Factor (eIF)	Inflammation/Immunology Cancer
Rocaglamide (Roc-A) is isolated from the genus Aglaia and can be used for coughs, injuries, asthma and inflammatory skin diseases. Rocaglamide is a potent inhibitor of NF-κB activation in T-cells. Rocaglamide is a potent and selective heat shock factor 1 (HSF1) activation inhibitor with an IC₅₀ of ~50 nM. Rocaglamide inhibits the function of the translation initiation factor eIF4A. Rocaglamide also has anticancer properties in leukemia ^[1] .

HY-100872

KRIBB11 15+ Cited Publications	HSP Apoptosis	Cancer
KRIBB11 is an inhibitor of Heat shock factor 1 (HSF1), with IC₅₀ of 1.2 μM.

HY-13207

ONX-0914 20+ Cited Publications PR-957	Proteasome Bacterial HIV	Infection Inflammation/Immunology
ONX-0914 (PR-957) is a selective inhibitor of low-molecular mass polypeptide-7 (LMP7), the chymotrypsin-like subunit of the immunoproteasome. ONX-0914 blocks cytokine production and attenuates progression of experimental arthritis. ONX-0914 is a noncompetitive irreversible inhibitor of the mycobacterial proteasome (K_i=5.2 μM). ONX-0914 reactivates latent HIV-1 through p-TEFb activation mediated by HSF-1 ^[1] .

HY-103000

HSF1A 3 Publications Verification	HSP	Cardiovascular Disease Cancer
HSF1A is a cell-permeable activator of heat shock transcription factor 1 (HSF1) ^[1]. HSF1A also acts as a specific inhibitor of TRiC/CCT. Chaperonin TCP-1 ring complex (TRiC)/chaperonin containing TCP-1 (CCT) plays a pivotal role in toxin translocation and/or refolding .

HY-138280

DTHIB 5+ Cited Publications	HSP	Cancer
DTHIB is a direct and selective heat shock factor 1 (HSF1) inhibitor with a K_d of 160 nM for *DTHIB binding to the HSF1* DNA binding domain (DBD). DTHIB inhibits HSF1** cancer gene signature (HSF1 CaSig) and selectively stimulates degradation of nuclear *HSF1*. DTHIB has potently anticancer activities and can be used for prostate cancer research ^[1].

HY-18669

ML346 5+ Cited Publications	HSP	Cancer
ML346 is an activator of Hsp70 expression and HSF-1 activity, with an EC₅₀ of 4.6 μM for Hsp70. ML346 restores protein folding in conformational disease models, without significant cytotoxicity or lack of specificity. ML346 induces specific increases in genes and protein effectors of the heat shock response (HSR), including chaperones such as Hsp70, Hsp40, and Hsp27 ^[1].

HY-101026

CCT251236 4 Publications Verification	HSP	Cancer
CCT251236 is an orally available pirin ligand from a heat shock transcription factor 1 (hsf1) phenotypic screen with an IC₅₀ of 19 nM for inhibition of HSF1-mediated HSP72 induction.

HY-145927

NXP800 3 Publications Verification CCT361814	HSP	Cancer
NXP800 (CCT361814) is a potent and orally active *heat shock factor 1 (HSF1) pathway* inhibitor. NXP800 has the potential for cancer research ^[1] .

HY-133961

Cholesterol β-D-glucoside Cholesteryl glucoside	HSP	Metabolic Disease
Cholesterol β-D-glucoside (Cholesteryl glucoside) is a heat shock transcription factor 1 (HSF1) activator. Cholesterol β-D-glucoside induces HSP70 in fibroblast cells ^[1].

HY-107599

AEG3482	JNK Apoptosis	Neurological Disease
AEG3482 is a potent antiapoptotic compound that inhibits Jun kinase (JNK) activity through induced expression of heat shock protein 70 (HSP70). AEG3482 directly binds HSP90, thereby facilitating *HSF1*-dependent expression of HSP70 and HSP25 ^[1].

HY-149127

Rosolutamide ASC-JM17; ALZ-003	Keap1-Nrf2 Androgen Receptor HSP Mitophagy	Metabolic Disease
Rosolutamide (ASC-JM17), a curcumin analog, is an orally active, potent *Nrf1* and Nrf2 activator. Rosolutamide activates Nrf1, Nrf2 and heat shock factor 1 (Hsf1), thereby activating the expression of proteasome subunits, antioxidant enzymes and molecular chaperones. Rosolutamide degrades the polyglutamine (polyQ) androgen receptor (AR) via the ubiquitin-proteasome pathway and improves motor function in mouse models of spinal and bulbar muscular atrophy (SBMA). Rosolutamide improves mitochondrial function and promotes autophagy, decreases mutant protein aggregates, and attenuates intracellular/mitochondrial reactive oxygen species (ROS) levels ^[1] .

HY-N0754

Eupalinolide A	YAP HSP Reactive Oxygen Species (ROS) ERK Autophagy Apoptosis Tyrosinase DNA/RNA Synthesis	Neurological Disease Inflammation/Immunology Cancer
Eupalinolide A is a Yes-associated protein (YAP) degrader and HSP70 inducer. Eupalinolide A inhibits osteogenic differentiation of tendon-derived stem cells (TDSCs). Eupalinolide A induces autophagy in hepatocellular carcinoma cells via activating the ROS/ERK signaling pathway. Eupalinolide A protects PAM212 cells from UVB-, Menadione (HY-B0332)-, or heat shock-induced apoptosis. Eupalinolide A alleviates trauma-induced heterotopic ossification (HO) of Achilles tendon and inhibits growth of MHCC97-L and HCCLM3 hepatocellular carcinoma xenograft tumors in mice. Eupalinolide A can be used for the study of traumatic heterotopic ossification of tendons and hepatocellular carcinoma ^[1] .

HY-13207A

ONX-0914 TFA 20+ Cited Publications PR-957 TFA	Proteasome Bacterial HIV	Infection Inflammation/Immunology
ONX-0914 (PR-957) TFA is a selective inhibitor of low-molecular mass polypeptide-7 (LMP7), the chymotrypsin-like subunit of the immunoproteasome. ONX-0914 TFA blocks cytokine production and attenuates progression of experimental arthritis. ONX-0914 TFA is a noncompetitive irreversible inhibitor of the mycobacterial proteasome (K_i=5.2 μM). ONX-0914 TFA reactivates latent HIV-1 through p-TEFb activation mediated by HSF-1 ^[1] .

HY-W224634

HSF1-IN-2	HSP	Cancer
HSF1-IN-2 (Compound 0048) is a *HSF1* inhibitor. HSF1-IN-2 is applicable to cancer research ^[1].

HY-RS06407

Hsf1 Mouse Pre-designed siRNA Set A	Small Interfering RNA (siRNA) HSP	Others
Hsf1 Mouse Pre-designed siRNA Set A contains three designed siRNAs for Hsf1 gene (Mouse), as well as a negative control, a positive control, and a FAM-labeled negative control.

Hsf1 Mouse Pre-designed siRNA Set A Hsf1 Mouse Pre-designed siRNA Set A

HY-RS06406

HSF1 Human Pre-designed siRNA Set A	Small Interfering RNA (siRNA) HSP	Others
HSF1 Human Pre-designed siRNA Set A contains three designed siRNAs for HSF1 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

HSF1 Human Pre-designed siRNA Set A HSF1 Human Pre-designed siRNA Set A

HY-RS06408

Hsf1 Rat Pre-designed siRNA Set A	Small Interfering RNA (siRNA) HSP	Others
Hsf1 Rat Pre-designed siRNA Set A contains three designed siRNAs for Hsf1 gene (Rat), as well as a negative control, a positive control, and a FAM-labeled negative control.

Hsf1 Rat Pre-designed siRNA Set A Hsf1 Rat Pre-designed siRNA Set A

HY-144867

CCT245232	HSP	Cancer
CCT245232 is a potent inhibitor of heat shock factor 1 (HSF1). HSF1 is the master regulator of the heat shock response, in which multiple genes are induced in response to temperature increase and other stresses. CCT245232 has the potential for the research of proliferative diseases, such as cancer (extracted from patent WO2015049535A1) ^[1].

HY-N3377

Liriodendrin	HSP	Others
Liriodendrin is an *HSF1* agonist can be isolated from E. ulmoides ^[1].

HY-N9615

Azadiradione	HSP	Infection Neurological Disease Inflammation/Immunology
Azadiradione is a bioactive limonoid found in Azadirachta indica. Azadiradione is a *HSF1* activator. Azadiradione has antimycobacterial, anti-nociceptive and anti-inflammatory activities ^[1] .

HY-19356B

(+)-Rocaglamide	Drug Derivative NF-κB HSP Eukaryotic Initiation Factor (eIF)	Inflammation/Immunology Cancer
(+)-Rocaglamide is the dextrorotatory enantiomer of Rocaglamide (HY-19356). Rocaglamide (Roc-A) is isolated from the genus Aglaia and can be used for coughs, injuries, asthma and inflammatory skin diseases. Rocaglamide is a potent inhibitor of NF-κB activation in T-cells. Rocaglamide is a potent and selective heat shock factor 1 (HSF1) activation inhibitor with an IC₅₀ of 50 nM. Rocaglamide inhibits the function of the translation initiation factor eIF4A. Rocaglamide also has anticancer properties in leukemia ^[1] .

HY-167961

HSF1-IN-1	HSP	Cancer
HSF1-IN-1 (page 71, compound 1) is a heat shock factor 1 (HSF1) inhibitor. HSF1-IN-1 inhibit stress-induced expression from heat shock gene promoters. HSF1-IN-1 can be used for the study of cancer ^[1].

HY-181808

HSF1/AMPK activator 1	AMPK TGF-beta/Smad Collagen	Metabolic Disease
HSF1/AMPK activator 1 is a compound that modulates the *HSF1/AMPK* axis and the *TGF-β1/Smad* signaling pathway. HSF1/AMPK activator 1 exhibits anti-hepatic fibrosis activity and metabolic stability. HSF1/AMPK activator 1 inhibits fibrosis formation and cell proliferation in activated hepatic stellate cells. HSF1/AMPK activator 1 alleviates liver injury and hepatic fibrosis symptoms in fibrotic mice. HSF1/AMPK activator 1 is applicable to research related to hepatic fibrosis ^[1].

HY-174438

PSEC13	HSP	Metabolic Disease
PSEC13 is an activator of *HSF-1/DAF-16* axis. PSEC13 can upregulate heat shock proteins. PSEC13 can form hydrogen bonds with key residues in the HSP-16.2 active site. PSEC13 can be used to enhance proteostasis and extend lifespan through the modulation of HSP-16.2. PSEC13 could promote the nuclear translocation of daf-16, upgrading the proportion of intermediate. PSEC13 can be studied in research for aging and age-related diseases ^[1].

HY-N12887

Mycothiazole	Mitochondrial Metabolism	Others Cancer
Mycothiazole is an inhibitor for mitochondrial electron transport chain (ETC) complex I. Mycothiazole exhibits cytotoxicity in cancer cells Huh7 (IC₅₀ is 55.8 μM), U87 and MCF7. Mycothiazole induces apoptosis in Huh7. Mycothiazole utilizes the unfolded protein response (UPR) and heat shock response (HSR) pathway involved transcription factors ATFS-1 and HSF1, to extend the lifespan of C. elegans ^[1].

HY-103000R

HSF1A (Standard)	Reference Standards HSP	Cardiovascular Disease Cancer
HSF1A (Standard) is the analytical standard of HSF1A (HY-103000). This product is intended for research and analytical applications. HSF1A is a cell-permeable activator of heat shock transcription factor 1 (HSF1) ^[1]. HSF1A also acts as a specific inhibitor of TRiC/CCT. Chaperonin TCP-1 ring complex (TRiC)/chaperonin containing TCP-1 (CCT) plays a pivotal role in toxin translocation and/or refolding .

HY-101026R

CCT251236 (Standard)	HSP Reference Standards	Cancer
CCT251236 (Standard) is the analytical standard of CCT251236 (HY-101026). This product is intended for research and analytical applications. CCT251236 is an orally available pirin ligand from a heat shock transcription factor 1 (hsf1) phenotypic screen with an IC50 of 19 nM for inhibition of HSF1-mediated HSP72 induction.

HY-107599R

AEG3482 (Standard)	Reference Standards JNK Apoptosis	Neurological Disease
AEG3482 (Standard) is the analytical standard of AEG3482 (HY-107599). This product is intended for research and analytical applications. AEG3482 is a potent antiapoptotic compound that inhibits Jun K_inase (JNK) activity through induced expression of heat shock protein 70 (HSP70). AEG3482 directly binds HSP90, thereby facilitating HSF1-dependent expression of HSP70 and HSP25 ^[1].

HY-N17756

Withanolide D	HSP	Cancer
Withanolide D (Compound 2) is a steroidal ester found in Withania somnifera (L.) Dunal, with anticancer activity. Withanolide D can activate the heat-shock factor 1 (HSF1)-dependent stress response. Withanolide D can be used for the research of cancer such as lymphoma ^[1].

HY-100872R

KRIBB11 (Standard)	HSP Reference Standards Apoptosis	Cancer
KRIBB11 (Standard) is the analytical standard of KRIBB11 (HY-100872). This product is intended for research and analytical applications. KRIBB11 is an inhibitor of Heat shock factor 1 (HSF1), with IC50 of 1.2 μM.

HY-123303

NSC-134754 NZ-28	HSP	Cancer
NSC-134754 is a dehydroemetine derivative and heat shock protein induction inhibitor. NSC-134754 acts at the post-transcriptional level, targets Hsp72 and Hsp27, and does not alter general protein synthesis, *HSF-1* transcriptional activity, or Hsp mRNA levels. NSC-134754 shows no significant toxicity in preclinical models and sensitizes cancer cells to proteasome and Hsp90 inhibitors. NSC-134754 can be used for the research of multiple myeloma, prostate carcinoma, colon carcinoma ^[1].

HY-162363

MD6a	PARP	Neurological Disease
MD6a is a melatonin derivative with inhibitroy activity towards *PARP-1, which maintains proteins hemostasis and improves mitochondrial function through TOR/HSF-1* signaling. MD6a a neuroprotective effect ^[1].

HY-162515

8-OAc	Mitochondrial Metabolism	Cancer
8-OAc is a potent and selective mitochondrial electron transport chain (ETC) complex I inhibitor. 8-OAc exhibits cytotoxicity against cancer cell lines ^[1].

HY-RS09553

NR5A1 Human Pre-designed siRNA Set A	Small Interfering RNA (siRNA)	Others
NR5A1 Human Pre-designed siRNA Set A contains three designed siRNAs for NR5A1 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

NR5A1 Human Pre-designed siRNA Set A NR5A1 Human Pre-designed siRNA Set A

HY-164184

Ly101-4B	Apoptosis Caspase HSP Early 2 Factor (E2F) DNA/RNA Synthesis	Cancer
Ly101-4B is an apoptosis inducer and multi-target inhibitor with antiproliferative, antitumor and cycytotoxic effects. Ly101-4B reduces *HSF1* expression, inhibits microRNA-214 synthesis, downregulates HSP27, HSP70 and HSP90 expression, while suppressing E2F-dependent transcriptional activity and downregulating its target genes. Ly101-4B induces caspase 3/7-mediated apoptosis by reducing DNA synthesis, inhibiting the cell cycle and G1/S phase transition, without affecting RNA synthesis or inducing necrosis. Ly101-4B is selective for pancreatic ductal adenocarcinoma cells with different genotypes and varying degrees of E2F dependence. Ly101-4B can be used in research related to epithelial ovarian cancer and pancreatic ductal adenocarcinoma ^[1] .

HY-181794

Z19024498	Apoptosis	Cancer
Z19024498 is a heat sensitizer. Z19024498 inhibits SAFB granule formation under heat stress conditions. Z19024498 enhances heat stress-induced Apoptosis. Z19024498 exerts anticancer activity against cervical cancer in synergy with heat stress ^[1].

Rocaglamide 25+ Cited Publications Roc-A	Alkaloids Classification of Application Fields Other Alkaloids Plants Meliaceae Disease Research Fields Aglaia elliptifolia Source Classification Cancer	NF-κB HSP Eukaryotic Initiation Factor (eIF)
Rocaglamide (Roc-A) is isolated from the genus Aglaia and can be used for coughs, injuries, asthma and inflammatory skin diseases. Rocaglamide is a potent inhibitor of NF-κB activation in T-cells. Rocaglamide is a potent and selective heat shock factor 1 (HSF1) activation inhibitor with an IC₅₀ of ~50 nM. Rocaglamide inhibits the function of the translation initiation factor eIF4A. Rocaglamide also has anticancer properties in leukemia ^[1] .

Eupalinolide A	Structural Classification Classification of Application Fields Melilotus albus Desr. Terpenoids Sesquiterpenes Plants Compositae Inflammation/Immunology Disease Research Fields Source Classification	YAP HSP Reactive Oxygen Species (ROS) ERK Autophagy Apoptosis Tyrosinase DNA/RNA Synthesis
Eupalinolide A is a Yes-associated protein (YAP) degrader and HSP70 inducer. Eupalinolide A inhibits osteogenic differentiation of tendon-derived stem cells (TDSCs). Eupalinolide A induces autophagy in hepatocellular carcinoma cells via activating the ROS/ERK signaling pathway. Eupalinolide A protects PAM212 cells from UVB-, Menadione (HY-B0332)-, or heat shock-induced apoptosis. Eupalinolide A alleviates trauma-induced heterotopic ossification (HO) of Achilles tendon and inhibits growth of MHCC97-L and HCCLM3 hepatocellular carcinoma xenograft tumors in mice. Eupalinolide A can be used for the study of traumatic heterotopic ossification of tendons and hepatocellular carcinoma ^[1] .

Liriodendrin	Structural Classification Eucommia ulmoides Oliver Lignans Eucommiaceae Phenylpropanoids Plants Source Classification	HSP
Liriodendrin is an *HSF1* agonist can be isolated from E. ulmoides ^[1].

Azadiradione	Triterpenes other families Neurological Disease Classification of Application Fields Terpenoids Plants Inflammation/Immunology Disease Research Fields Biological Pesticide Research Agricultural Research Source Classification	HSP
Azadiradione is a bioactive limonoid found in Azadirachta indica. Azadiradione is a *HSF1* activator. Azadiradione has antimycobacterial, anti-nociceptive and anti-inflammatory activities ^[1] .

Mycothiazole	Natural Products Marine natural products Sponge Source Classification	Mitochondrial Metabolism
Mycothiazole is an inhibitor for mitochondrial electron transport chain (ETC) complex I. Mycothiazole exhibits cytotoxicity in cancer cells Huh7 (IC₅₀ is 55.8 μM), U87 and MCF7. Mycothiazole induces apoptosis in Huh7. Mycothiazole utilizes the unfolded protein response (UPR) and heat shock response (HSR) pathway involved transcription factors ATFS-1 and HSF1, to extend the lifespan of C. elegans ^[1].

Withanolide D	Structural Classification Microorganisms Ketones, Aldehydes, Acids Source Classification	HSP
Withanolide D (Compound 2) is a steroidal ester found in Withania somnifera (L.) Dunal, with anticancer activity. Withanolide D can activate the heat-shock factor 1 (HSF1)-dependent stress response. Withanolide D can be used for the research of cancer such as lymphoma ^[1].

Cat. No.	Compare	Product Name	Species	Source	Image

HY-P73918

	HSF1 Protein, Human (His) Heat shock factor protein 1; hsf1; HSTF 1	Human	E. coli
	HSF1 is a stress-inducible transcription factor that coordinates the heat shock response by binding to the heat shock element (HSE) and activating heat shock genes. In unstressed cells, it remains inactive in multichaperone complexes. HSF1 Protein, Human (His) is the recombinant human-derived HSF1 protein, expressed by E. coli , with N-6*His labeled tag.

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Host:	Mouse (1) Rabbit (7)
Reactivity:	Human (8) Rat (2) Mouse (4)
Application:	IHC-P (7) ICC/IF (3) IP (2) IHC-F (2) WB (7) FC (3)
Isotype:	IgG (7) IgG2 (1)
Conjugation:	Non-conjugated (8)
Clonality:	Monoclonal (6) Recombinant (4)
Modification:	Phosphorylated (3) Unmodified (3)

Cat. No.	Compare	Product Name	Application	Reactivity	Image

HY-P81052

	HSF1 Antibody (YA896) hsf1; HSTF1; Heat shock factor protein 1; hsf 1; Heat shock transcription factor 1; HSTF 1	WB, IHC-P, ICC/IF, IP, FC	Human
	HSF1 Antibody (YA896) is a Rabbit-derived and non-conjugated IgG monoclonal antibody, targeting to HSF1.

HY-P81050

	*Phospho-HSF1* (Ser326) Antibody(YA894)** 1 Publications Verification hsf1; HSTF1; Heat shock factor protein 1; hsf 1; Heat shock transcription factor 1; HSTF 1	WB, IHC-P, IP	Human
	Phospho-HSF1 (Ser326) Antibody(YA894) is a Rabbit-derived and non-conjugated IgG monoclonal antibody, targeting to Phospho-HSF1 (Ser326).

HY-P86671

	*phospho-HSF1* (Ser326) Antibody (YA6363)** hsf1(S326); hsf1(phospho S326); p-hsf1(phospho S326); Heat shock factor 1; Heat shock factor protein 1; Heat shock transcription factor 1; hsf 1; hsf1; HSTF 1; HSTF1; hsf1_HUMAN.	WB, IHC-P, IHC-F, ICC/IF, FC	Human, Mouse
	phospho-HSF1 (Ser326) Antibody (YA6363) is a Rabbit-derived and non-conjugated IgG monoclonal antibody, targeting to phospho-HSF1 (Ser326).

HY-P86671A

	*phospho-HSF1* (Ser326) Antibody (YA6363)(PBS only)** hsf1(S326); hsf1(phospho S326); p-hsf1(phospho S326); Heat shock factor 1; Heat shock factor protein 1; Heat shock transcription factor 1; hsf 1; hsf1; HSTF 1; HSTF1; hsf1_HUMAN.	WB, IHC-P, IHC-F, ICC/IF, FC	Human, Mouse
	phospho-HSF1 (Ser326) Antibody (YA6363) is a Rabbit-derived and non-conjugated IgG monoclonal antibody, targeting to phospho-HSF1 (Ser326).

HY-P80822

	*Phospho-HSF1* (Ser303/Ser307) Antibody (YA188)** hsf1; HSTF1; Heat shock factor protein 1; hsf 1; Heat shock transcription factor 1; HSTF 1	WB, IHC-P	Human
	Phospho-HSF1 (Ser303/Ser307) Antibody (YA188) is a Rabbit-derived and non-conjugated IgG monoclonal antibody, targeting to Phospho-HSF1 (Ser303/Ser307).

HY-P80822A

	*Phospho-HSF1* (Ser303/Ser307) Antibody (YA188)(PBS only)** hsf1; HSTF1; Heat shock factor protein 1; hsf 1; Heat shock transcription factor 1; HSTF 1	WB, IHC-P	Human
	Phospho-HSF1 (Ser303/Ser307) Antibody (YA188) is a Rabbit-derived and non-conjugated IgG monoclonal antibody, targeting to Phospho-HSF1 (Ser303/Ser307).

HY-P83421

	Steroidogenic Factor 1 Antibody (YA3166) AD4BP; ELP; FTZ1; FTZF1; hsf 1; NR5A1; POF7; SF1; SPGF8; SRXY3; STF1; SF-1	WB	Human, Mouse, Rat
	Steroidogenic Factor 1 Antibody (YA3166) is a Rabbit-derived and non-conjugated IgG monoclonal antibody, targeting to Steroidogenic Factor 1.

HY-P810352

	Steroidogenic Factor 1 Antibody (YA9674) AD4BP, ELP, FTZ1, FTZF1, hsf-1, POF7, SF-1, SF1, SPGF8, SRXY3	IHC-P	Human, Mouse, Rat
	Steroidogenic Factor 1 Antibody (YA9674) is a Mouse-derived and non-conjugated IgG2 Monoclonal antibody, targeting to Steroidogenic Factor 1.

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