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Immunofluorescent analysis of Heat Shock Protein 70 using Heat Shock Protein 70 Monoclonal antibody (3A3) (Product# MA3-006) shows staining in HeLa cells. Heat Shock Protein 70 staining (green), F-Actin staining with Phalloidin (red) and nuclei with DAPI (blue) is shown. Cells were grown on chamber slides and fixed with formaldehyde prior to staining. Cells were probed without (control) or with or an antibody recognizing Heat Shock Protein 70 (Product# MA3-006) at a dilution of 1:100-1:200 over night at 4 °C, washed with PBS and incubated with a DyLight-488 conjugated secondary antibody (Product# 35552 for GAR, Product# 35503 for GAM). Images were taken at 60X magnification.
|Tested species reactivity||Amphibian, Arthropod, Avian, Fruit fly, Fish, Human, Mollusca, Mouse, Primate, Plant, Pig, Rat, Yeast|
|Published species reactivity||Yeast, Pig, Rat, Insect, Primate, Mollusca, Amphibian, Arthropod, Fish, Mouse, Human, Echinodermata, Not Applicable, Fruit fly|
|Host / Isotype||Mouse / IgG1|
|Immunogen||Human recombinant HSP70 overexpressed in E. coli.|
|Storage buffer||ascites diluted in PBS|
|Contains||0.05% sodium azide|
|Storage Conditions||-20° C, Avoid Freeze/Thaw Cycles|
|Tested Applications||Dilution *|
|Gel Shift (GS)||Assay dependent|
|Immunohistochemistry (Paraffin) (IHC (P))||1:200|
|Immunoprecipitation (IP)||2 µl|
|Western Blot (WB)||1:1000 - 1:5000|
* Suggested working dilutions are given as a guide only. It is recommended that the user titrate the product for use in their own experiment using appropriate negative and positive controls.
|Immunohistochemistry (IHC)||See 1 publications below|
|Western Blot (WB)||See 48 publications below|
|Immunocytochemistry (ICC)||See 2 publications below|
|Blocking Assay (BLOCK)||See 1 publications below|
|Immunoprecipitation (IP)||See 2 publications below|
|Flow Cytometry (Flow)||See 1 publications below|
|ELISA (ELISA)||See 2 publications below|
MA3-006 detects several members of the heat shock protein 70 kDa (HSP70) gene family including HSP70, HSC70, p75, and following heat shock, HSP72 from yeast, Drosophila, fish, porcine, plant, mouse, avian, arthropod (red claw crayfish & black tiger prawn), amphibian, non-human primate, and human samples.
MA3-006 has been successfully used in Western blot, immunocytochemistry, immunofluorescence, gel shift, and immunoprecipitation procedures. By Western blot, this antibody detects proteins from ~70 kDa to ~78 kDa representing different members of the HSP70 family. 2-dimensional gel electrophoresis is required to resolve the heat induced form of these proteins from their constitutively expressed counterparts. Immunocytochemical staining of HSP70 in heat shocked HeLa cells with MA3-006 results in cytoplasmic staining.
The MA3-006 antigen is recombinant human HSP70 over-expressed in E. coli. Epitope mapping with a panel of HSP70 deletion mutants suggests that the epitope recognized is located between amino acids 504-617 of human HSP70, a region that has been shown to be involved in stress-induced nucleolar localization.
Heat shock proteins (HSP) are expressed in response to various biological stresses, including high temperatures. There are several major families of HSPs including HSP70, HSP90 and HSP100. The HSP70 family is a set of highly conserved proteins that are induced by a variety of biological stresses, including heat stress, in every organism in which the proteins have been examined. The human HSP70 family members include: HSP70, a protein which is strongly inducible in all organisms but which is also constitutively expressed in primate cells; HSP72, a 72 kDa protein that is induced exclusively under stress conditions; HSC70, or cognate protein, is a 72 kDa, constitutively expressed, protein which is involved in the uncoating of clathrin coated vesicles; GRP78, or BiP, is a glucose regulated 78 kDa protein localized in the endoplasmic reticulum; and p75, or HSP75, a 75 kDa protein that is found within the mitochondria.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
Histological, ultrastructural and heat shock protein 70 (HSP70) responses to heat stress in the sea cucumber Apostichopus japonicus.
MA3-006 was used in immunohistochemistry and western blot to study HSP70 in Apostichopus japonicus
|Xu D,Sun L,Liu S,Zhang L,Yang H||Fish & shellfish immunology (45:321)||2015|
Contrasting roles for MyoD in organizing myogenic promoter structures during embryonic skeletal muscle development.
MA3-006 was used in western blot to study the temporal regulation of MyoD in skeletal muscle differentiation
|Cho OH,Mallappa C,Hernández-Hernández JM,Rivera-Pérez JA,Imbalzano AN||Developmental dynamics : an official publication of the American Association of Anatomists (244:43)||2015|
Environmental heat stress induces epigenetic transgenerational inheritance of robustness in parthenogenetic Artemia model.
MA3-006 was used in western blot to study epigenetic transgenerational inheritance of heat stress tolerance in parthenogenetic Artemia
|Norouzitallab P,Baruah K,Vandegehuchte M,Van Stappen G,Catania F,Vanden Bussche J,Vanhaecke L,Sorgeloos P,Bossier P||FASEB journal : official publication of the Federation of American Societies for Experimental Biology (28:3552)||2014|
Non-lethal heat shock increased Hsp70 and immune protein transcripts but not Vibrio tolerance in the white-leg shrimp.
MA3-006 was used in western blot to study the lack of effect of abrupt heat shock on the susceptibility of white-leg shrimp to Vibrio infection despite increased expression of Hsp70 and immune-related proteins
|Loc NH,Macrae TH,Musa N,Bin Abdullah MD,Abdul Wahid ME,Sung YY||PloS one (8:null)||2013|
Enhancement of Hsp70 synthesis protects common carp, Cyprinus carpio L., against lethal ammonia toxicity.
MA3-006 was used in western blot to study the ability of a prickly pear cactus extract to increase Hsp70 levels and protect common carp against ammonia toxicity
|Sung YY,Roberts RJ,Bossier P||Journal of fish diseases (35:563)||2012|
The oncogenic TBC domain protein USP6/TRE17 regulates cell migration and cytokinesis.
MA3-006 was used in western blot to investigate the important role of USP6 in regulation of cell migration and division
|Rueckert C,Haucke V||Biology of the cell / under the auspices of the European Cell Biology Organization (104:22)||2012|
Priming the prophenoloxidase system of Artemia franciscana by heat shock proteins protects against Vibrio campbellii challenge.
MA3-006 was used in western blot to detect immune system priming by heat shock protein 70
|Baruah K,Ranjan J,Sorgeloos P,Macrae TH,Bossier P||Fish & shellfish immunology (31:134)||2011|
Does domestication process affect stress response in juvenile Eurasian perch Perca fluviatilis?
MA3-006 was used in western blot to study the effect of domestication on the stress response in juvenile Eurasian perch Perca fluviatilis
|Douxfils J,Mandiki SN,Marotte G,Wang N,Silvestre F,Milla S,Henrotte E,Vandecan M,Rougeot C,Mélard C,Kestemont P||Comparative biochemistry and physiology. Part A, Molecular & integrative physiology (159:92)||2011|
NF-κB is not directly responsible for photoresistance induced by fractionated light delivery in HT-29 colon adenocarcinoma cells.
MA3-006 was used in western blot to investigate molecular mechanisms of the photoresistance on HT-29 cells
|Kuliková L,Mikeš J,Hýžďalová M,Palumbo G,Fedoročko P||Photochemistry and photobiology (86:1285)||2010|
Level of heat shock proteins decreases in individuals carrying B-chromosomes in the grasshopper Eyprepocnemis plorans.
MA3-006 was used in western blot to investigate the effect of B-chromosome on heat shock protein expression in Eyprepocnemis plorans
|Teruel M,Sørensen JG,Loeschcke V,Cabrero J,Perfectti F,Camacho JP||Cytogenetic and genome research (132:94)||2010|
Efficacy of heterologous and homologous heat shock protein 70s as protective agents to Artemia franciscana challenged with Vibrio campbellii.
MA3-006 was used in western blot to investigate the effect of different Hsp70 on protection against Vibrio campbellii
|Baruah K,Ranjan J,Sorgeloos P,Bossier P||Fish & shellfish immunology (29:733)||2010|
Do historical sediments of pulp and paper industry contribute to the exposure of fish caged in receiving waters?
MA3-006 was used in western blot to investigate the environmental influence of paper mills for fish health
|Oikari A,Lahti M,Meriläinen P,Afanasyev S,Krasnov A||Journal of environmental monitoring : JEM (12:1045)||2010|
The role of p53 in the efficiency of photodynamic therapy with hypericin and subsequent long-term survival of colon cancer cells.
MA3-006 was used in western blot to study the effect of p53 expression on the efficacy of photodynamic therapy and colon cancer recurrence
|Mikes J,Koval' J,Jendzelovský R,Sacková V,Uhrinová I,Kello M,Kuliková L,Fedorocko P||Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology (8:1558)||2009|
Oxidative stress, protein carbonylation and heat shock proteins in the black tiger shrimp, Penaeus monodon, following exposure to endosulfan and deltamethrin.
MA3-006 was used in western blot to study the cellular changes in the black tiger shrimp Penaeus monodon in response to
|Dorts J,Silvestre F,Tu HT,Tyberghein AE,Phuong NT,Kestemont P||Environmental toxicology and pharmacology (28:302)||2009|
Surface expression of a C-terminal alpha-helix region in heat shock protein 72 on murine LL/2 lung carcinoma can be recognized by innate immune sentinels.
MA3-006 was used in western blot to study the induction of heat shock protein 72 expression in murine LL/2 lung carcinoma
|Tani F,Ohno M,Furukawa Y,Sakamoto M,Masuda S,Kitabatake N||Molecular immunology (46:1326)||2009|
Bioinformatics and protein expression analyses implicate LEA proteins in the drought response of Collembola.
MA3-006 was used in western blot to investigate the role of late embryogenesis abundant proteins in the drought response of Collembola
|Bahrndorff S,Tunnacliffe A,Wise MJ,McGee B,Holmstrup M,Loeschcke V||Journal of insect physiology (55:210)||2009|
Sex-, gametogenesis, and tidal height-related differences in levels of HSP70 and metallothioneins in the Pacific oyster Crassostrea gigas.
MA3-006 was used in western blot to study the effect of gene, gametogenesis, and tidal height on heat shock protein 70 and metallothionein expression in the Pacific oyster Crassostrea gigas
|Meistertzheim AL,Lejart M,Le Goïc N,Thébault MT||Comparative biochemistry and physiology. Part A, Molecular & integrative physiology (152:234)||2009|
The effects of treated effluents on the intensity of papillomatosis and HSP70 expression in roach.
MA3-006 was used in western blot to investigate the influence of treated pulp mill and municipal effluents on papillomatosis and heat shock protein 70 expression in Rutilus rutilus
|Korkea-aho TL,Vehniäinen ER,Kukkonen JV,Taskinen J||Ecotoxicology and environmental safety (70:462)||2008|
Dimeric heat shock protein 40 binds radial spokes for generating coupled power strokes and recovery strokes of 9 + 2 flagella.
MA3-006 was used in western blot to study the role of dimeric heat shock protein 40 in flagella function.
|Yang C,Owen HA,Yang P||The Journal of cell biology (180:403)||2008|
Saccharomyces cerevisiae strains from traditional fermentations of Brazilian cachaça: trehalose metabolism, heat and ethanol resistance.
MA3-006 was used in western blot to investigate the trehalose metabolism of cachaca S. cerevisiae strains under stress conditions
|Vianna CR,Silva CL,Neves MJ,Rosa CA||Antonie van Leeuwenhoek (93:205)||2007|
Synergistic impacts of heat shock and spawning on the physiology and immune health of Crassostrea gigas: an explanation for summer mortality in Pacific oysters.
MA3-006 was used in western blot to study how spawning affects thermotolerance in the Pacific oyster in summer with extremely high temperature
|Li Y,Qin JG,Abbott CA,Li X,Benkendorff K||American journal of physiology. Regulatory, integrative and comparative physiology (293:R2353)||2007|
Heat shock protein (hsp70) expression and thermal tolerance in sublethally heat-shocked eastern oysters Crassostrea virginica infected with the parasite Perkinsus marinus.
MA3-006 was used in western blot to investigate the protective effect of sublethal heat shock on Crassostrea virginica with Perkinsus marinus infection against lethal heat stress
|Encomio VG,Chu FL||Diseases of aquatic organisms (76:251)||2007|
Is HSP70 involved in acclimation to cadmium in the Chinese crab, Eriocheir sinensis ?
MA3-006 was used in western blot to investigate the influence of heat shock protein 70 on Chinese crab acclimation to cadmium
|Silvestre F,Trausch G,Devos P||Bulletin of environmental contamination and toxicology (78:432)||2007|
Non-lethal heat shock protects gnotobiotic Artemia franciscana larvae against virulent Vibrios.
MA3-006 was used in western blot to study the role of non-lethal heat shock in protecting gnotobiotic Artemia franciscana larvae against virulent Vibrios
|Yik Sung Y,Van Damme EJ,Sorgeloos P,Bossier P||Fish & shellfish immunology (22:318)||2007|
Multiscale approach of fish responses to different types of environmental contaminations: a case study.
MA3-006 was used in western blot to investigate the fish responses to environmental contaminations
|Mayon N,Bertrand A,Leroy D,Malbrouck C,Mandiki SN,Silvestre F,Goffart A,Thomé JP,Kestemont P||The Science of the total environment (367:715)||2006|
Stress protein response in two sibling species of Marenzelleria (Polychaeta: Spionidae): is there an influence of acclimation salinity?
MA3-006 was used in western blot to study the effect of acclimation salinity on the stress protein response in two sibling species of Marenzelleria
|Blank M,Bastrop R,Jürss K||Comparative biochemistry and physiology. Part B, Biochemistry & molecular biology (144:451)||2006|
Thermoprotection of synaptic transmission in a Drosophila heat shock factor mutant is accompanied by increased expression of Hsp83 and DnaJ-1.
MA3-006 was used in western blot to study the thermoprotective mechanism for a Drosophila heat shock factor mutant
|Neal SJ,Karunanithi S,Best A,So AK,Tanguay RM,Atwood HL,Westwood JT||Physiological genomics (25:493)||2006|
Temperature regulates hypoxia-inducible factor-1 (HIF-1) in a poikilothermic vertebrate, crucian carp (Carassius carassius).
MA3-006 was used in western blot to study the role of temperature in regulating hypoxia-inducible factor-1 expression in a poikilothermic fish
|Rissanen E,Tranberg HK,Sollid J,Nilsson GE,Nikinmaa M||The Journal of experimental biology (209:994)||2006|
ATP production in Chlamydomonas reinhardtii flagella by glycolytic enzymes.
MA3-006 was used in western blot to study the role of in situ ATP synthesis in normal flagellar motility.
|Mitchell BF,Pedersen LB,Feely M,Rosenbaum JL,Mitchell DR||Molecular biology of the cell (16:4509)||2005|
Characterization of a molecular chaperone present in the eukaryotic flagellum.
MA3-006 was used in western blot to study the role of the Hsp70 in the assembly and maintenance of the flagellum.
|Shapiro J,Ingram J,Johnson KA||Eukaryotic cell (4:1591)||2005|
Dimeric novel HSP40 is incorporated into the radial spoke complex during the assembly process in flagella.
MA3-006 was used in western blot to study the incorporation of a novel HSP40 into the radial spoke assembly during flagella assembly
|Yang C,Compton MM,Yang P||Molecular biology of the cell (16:637)||2005|
A field methodology to study effects of UV radiation on fish larvae.
MA3-006 was used in western blot to investigate the effects of UV radiation on fish larvae
|Häkkinen J,Oikari A||Water research (38:2891)||2004|
High sensitivity of northern pike larvae to UV-B but no UV-photoinduced toxicity of retene.
MA3-006 was used in western blot to investigate the influence of UV-B on northern pike larvae
|Häkkinen J,Vehniäinen E,Oikari A||Aquatic toxicology (Amsterdam, Netherlands) (66:393)||2004|
Peptidoglycan recognition protein tag7 forms a cytotoxic complex with heat shock protein 70 in solution and in lymphocytes.
MA3-006 was used in western blot to study the interaction between the peptidoglycan recognition protein tag7 and Hsp70 in solution and in lymphocytes
|Sashchenko LP,Dukhanina EA,Yashin DV,Shatalov YV,Romanova EA,Korobko EV,Demin AV,Lukyanova TI,Kabanova OD,Khaidukov SV,Kiselev SL,Gabibov AG,Gnuchev NV,Georgiev GP||The Journal of biological chemistry (279:2117)||2004|
Targeted disruption of the heat shock transcription factor (hsf)-2 gene results in increased embryonic lethality, neuronal defects, and reduced spermatogenesis.
MA3-006 was used in western blot to study the effects of heat shock transcription factor-2 knockout
|Wang G,Zhang J,Moskophidis D,Mivechi NF||Genesis (New York, N.Y. : 2000) (36:48)||2003|
Heat-shock protein (HSP70) response in the eastern oyster, Crassostrea virginica, exposed to PAHs sorbed to suspended artificial clay particles and to suspended field contaminated sediments.
MA3-006 was used in western blot to investigate the heat shock responses in the eastern oyster Crassostrea virginica
|Cruz-Rodríguez LA,Chu FL||Aquatic toxicology (Amsterdam, Netherlands) (60:157)||2002|
Multiple components of the HSP90 chaperone complex function in regulation of heat shock factor 1 In vivo.
MA3-006 was used in western blot to study the complexing process of heat shock factor 1 with the HSP90 chaperone machinery.
|Bharadwaj S,Ali A,Ovsenek N||Molecular and cellular biology (19:8033)||1999|
Heat shock response and protein degradation: regulation of HSF2 by the ubiquitin-proteasome pathway.
MA3-006 was used in western blot to investigate the regulation of heat shock transcription factor 2 by ubiquitin-proteasome
|Mathew A,Mathur SK,Morimoto RI||Molecular and cellular biology (18:5091)||1998|
Synthesis and turnover of embryonic sea urchin ciliary proteins during selective inhibition of tubulin synthesis and assembly.
MA3-006 was used in western blot to study the role of tubulin synthesis and assembly in sea urchin ciliogenesis.
|Stephens RE||Molecular biology of the cell (8:2187)||1997|
HSP70 binding sites in the tumor suppressor protein p53.
MA3-006 was used in western blot to identify the binding sites of HSP70 in p53
|Fourie AM,Hupp TR,Lane DP,Sang BC,Barbosa MS,Sambrook JF,Gething MJ||The Journal of biological chemistry (272:19471)||1997|
Transport of a novel complex in the cytoplasmic matrix of Chlamydomonas flagella.
MA3-006 was used in western blot to study the mechanisms for the protein transport important for maintaining Chlamydomonas flagella
|Piperno G,Mead K||Proceedings of the National Academy of Sciences of the United States of America (94:4457)||1997|
Identification of a molecular chaperone in the eukaryotic flagellum and its localization to the site of microtubule assembly.
MA3-006 was used in western blot to identify a molecular chaperone in the eukaryotic flagellum and investigate its localization
|Bloch MA,Johnson KA||Journal of cell science (108 ( Pt 11):3541)||1995|
The RCC1 protein interacts with Ran, RanBP1, hsc70, and a 340-kDa protein in Xenopus extracts.
MA3-006 was used in western blot to investigate the interactions of the RCC1 protein with Ran, RanBP1, hsc70, and a 340-kDa protein in Xenopus extracts
|Saitoh H,Dasso M||The Journal of biological chemistry (270:10658)||1995|
Cloning and subcellular localization of human mitochondrial hsp70.
MA3-006 was used in western blot to characterize human mitochondrial hsp70 and investigate its cellular distribution
|Bhattacharyya T,Karnezis AN,Murphy SP,Hoang T,Freeman BC,Phillips B,Morimoto RI||The Journal of biological chemistry (270:1705)||1995|
The stress response to loss of signal recognition particle function in Saccharomyces cerevisiae.
MA3-006 was used in western blot to investigate the consequences of depletion of SRP54p in budding yeast
|Arnold CE,Wittrup KD||The Journal of biological chemistry (269:30412)||1994|
Interaction between heat shock factor and hsp70 is insufficient to suppress induction of DNA-binding activity in vivo.
MA3-006 was used in western blot to investigate the association of heat shock factor with heat shock proteins and its effect on DNA-binding activity.
|Rabindran SK,Wisniewski J,Li L,Li GC,Wu C||Molecular and cellular biology (14:6552)||1994|
Pork quality and the expression of stress protein Hsp 70 in swine.
MA3-006 was used in western blot to study the expression of Hsp 70 in porcine tissue and to correlate its expression with porcine stress susceptibility
|van Laack RL,Faustman C,Sebranek JG||Journal of animal science (71:2958)||1993|
A constitutive form of heat-shock protein 70 is located in the outer membranes of mitochondria from rat liver.
MA3-006 was used in western blot to study the role of heat-shock protein 70 in the outer membranes of mitochondria from rat liver
|Lithgow T,Ryan M,Anderson RL,Høj PB,Hoogenraad NJ||FEBS letters (332:277)||1993|
T-complex polypeptide-1 is a subunit of a heteromeric particle in the eukaryotic cytosol.
MA3-006 was used in western blot to characterize the cytosolic T-complex polypeptide 1
|Lewis VA,Hynes GM,Zheng D,Saibil H,Willison K||Nature (358:249)||1992|
Thermal tolerance in juvenile King George whiting (Sillaginodes punctata) reduces as fish age and this reduction coincides with migration to deeper colder water.
MA3-006 was used in immunocytochemistry and western blot to study heat schock protein expression and thermal tolerance in juvenile and adult King George whiting
|Meakin CA,Qin JG,Pogson LD,Abbott CA||Comparative biochemistry and physiology. Part A, Molecular & integrative physiology (172:46)||2014|
Rapid glucocorticoid receptor exchange at a promoter is coupled to transcription and regulated by chaperones and proteasomes.
MA3-006 was used in immunocytochemistry to investigate the role of chaperones and proteasomes during glucocorticoid receptor exchange.
|Stavreva DA,Müller WG,Hager GL,Smith CL,McNally JG||Molecular and cellular biology (24:2682)||2004|
Different rotavirus strains enter MA104 cells through different endocytic pathways: the role of clathrin-mediated endocytosis.
MA3-006 was used in blocking/activating experiment to investigate the mechanism for the rotavirus entry into host cells
|Gutiérrez M,Isa P,Sánchez-San Martin C,Pérez-Vargas J,Espinosa R,Arias CF,López S||Journal of virology (84:9161)||2010|
Co-chaperones Bag-1, Hop and Hsp40 regulate Hsc70 and Hsp90 interactions with wild-type or mutant p53.
MA3-006 was used in immunoprecipitation to investigate the role of co-chaperones Bag-1, Hop and heat Shock Protein 40 in Hsc70 and heat Shock Protein 90 interactions with p53
|King FW,Wawrzynow A,Höhfeld J,Zylicz M||The EMBO journal (20:6297)||2001|
Regulation of the human hsp70 promoter by p53.
MA3-006 was used in immunoprecipitation to investigate the effect of p53 on HSP70 transcription
|Agoff SN,Hou J,Linzer DI,Wu B||Science (New York, N.Y.) (259:84)||1993|
Contribution of heat shock proteins to cell protection from complement-mediated lysis.
MA3-006 was used in flow cytometry to investigate the protective roles of heat shock proteins during complement-mediated lysis
|Fishelson Z,Hochman I,Greene LE,Eisenberg E||International immunology (13:983)||2001|
Individual subunits of the eukaryotic cytosolic chaperonin mediate interactions with binding sites located on subdomains of beta-actin.
MA3-006 was used in ELISA to determine the interaction of individual subunits of CCT with newly synthesized b-actin.
|Hynes GM,Willison KR||The Journal of biological chemistry (275:18985)||2000|
Effect of different environmental variables on the synthesis of Hsp70 in Raphidocelis subcapitata.
MA3-006 was used in ELISA to evaluate heat Shock Protein 70 in Raphidocelis subcapitata as an environmental monitor
|Bierkens J,Van de Perre WV,Maes J||Comparative biochemistry and physiology. Part A, Molecular & integrative physiology (120:29)||1998|
68 kDa heat shock protein; dnaK-type molecular chaperone HSP70-1; epididymis secretory protein Li 103; heat shock 70 kDa protein 1; heat shock 70 kDa protein 1/2; heat shock 70 kDa protein 1A; heat shock 70 kDa protein 1A/1B; heat shock 70 kDa protein 1B; heat shock 70 kDa protein 2; heat shock 70 kDa protein 3; heat shock 70kD protein 1A; heat shock 70kDa protein 1A; heat shock 70kDa protein 1B; heat shock protein 70-1; heat shock protein, 70 kDa 3; heat shock-induced protein; HSP70-1; HSP70-1/HSP70-2; HSP70-1A; HSP70.1/2; HSP70.1/HSP70.2; HSP70I; HSP72; HSPA1; inducible heat shock protein 70
HEL-S-103; hsp68; HSP70-1; HSP70-1A; Hsp70-2; Hsp70-3; HSP70.1; Hsp70.3; Hsp70A1; HSP70I; HSP72; HSPA1; HSPA1A; HSPA1B; Hspa2; HSX70; SBAB-707F1.4