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HSPA9 encodes a member of the heat shock protein 70 gene family. Additionally we are shipping HSPA9 Proteins (17) and HSPA9 Kits (1) and many more products for this protein.
Showing 10 out of 161 products:
Caenorhabditis elegans (C. elegans) Monoclonal HSPA9 Primary Antibody for ICC, IF - ABIN361740
Kaul, Wadhwa, Komatsu, Sugimoto, Mitsui: On the cytosolic and perinuclear mortalin: an insight by heat shock. in Biochemical and biophysical research communications 1993
Show all 12 references for ABIN361740
Human Polyclonal HSPA9 Primary Antibody for EIA, IF - ABIN784589
Leustek, Dalie, Amir-Shapira, Brot, Weissbach: A member of the Hsp70 family is localized in mitochondria and resembles Escherichia coli DnaK. in Proceedings of the National Academy of Sciences of the United States of America 1989
Show all 10 references for ABIN784589
Human Polyclonal HSPA9 Primary Antibody for EIA, WB - ABIN952636
Li, Xu, Ling, Yang, Wang, Li, Zhou, Wang, Liu: mot-2-Mediated cross talk between nuclear factor-B and p53 is involved in arsenite-induced tumorigenesis of human embryo lung fibroblast cells. in Environmental health perspectives 2010
Show all 5 references for ABIN952636
Dog (Canine) Polyclonal HSPA9 Primary Antibody for IP, IHC - ABIN2779292
Shi, Liu, Zhang, Qin, Zhang, Li, Chen: [Cloning and sequence analysis of the Meq gene of 4 Marek's disease virus isolates from China]. in Bing du xue bao = Chinese journal of virology / [bian ji, Bing du xue bao bian ji wei yuan hui] 2008
Show all 2 references for ABIN2779292
Caenorhabditis elegans (C. elegans) Monoclonal HSPA9 Primary Antibody for ICC, IF - ABIN2481675
Schneider, Berthold, Bauer, Dietmeier, Guiard, Brunner, Neupert: Mitochondrial Hsp70/MIM44 complex facilitates protein import. in Nature 1994
Biallelic mutations in HSPA9 are associated with the EVEN-PLUS syndrome of congenital malformations and skeletal dysplasia.
veratridine enhances transactivation of UBXN2A, resulting in upregulation of UBXN2A in the cytoplasm, where UBXN2A binds and inhibits the oncoprotein mortalin-2
Impaired stoichiometry between mtHsp40 and mtHsp70 promotes Opa1L cleavage, leading to cristae opening, decreased OXPHOS, and triggering of mitochondrial fragmentation after reduction in their chaperone function.
mutations in HSPA9 result in congenital sideroblastic anemia inherited as an autosomal recessive trait
Expression of mortalin decreased significantly in dopaminergic cells overexpressing A53T alpha-syn
Results present the functional structure of human mortalin showing at least two domains and interacts with adenosine nucleotides with high affinity depending on the presence of Mg2 (show MUC7 Antibodies)+ ions.
Mortalin is a key regulator of multiple signaling and metabolic pathways pivotal to medullary thyroid carcinoma cell survival and proliferation.
Human mot-1 (show BTAF1 Antibodies), R126W, or P509S mutants lack mot-2 functions involved in carcinogenesis.
Glutamine (show GFPT1 Antibodies) regulated ubiquitination processes of Grp75 and Apg-2 (show HSPA4 Antibodies).
The functional interaction of mortalin with Parkin (show PARK2 Antibodies) and PINK1 (show PINK1 Antibodies), was investigated.
data imply a role for Hspa9 in B lymphopoiesis and Stat5 (show STAT5A Antibodies) activation downstream of IL-7 (show IL7 Antibodies) signaling
Matrin 3 (show MATR3 Antibodies) interacts specifically with the heat shock proteins glucose-regulated protein 78 (show HSPA5 Antibodies), GRP75 and glutathione S-transferase (show GSTa2 Antibodies) pi isoform 2.
down-regulation of mortalin may potentiate Abeta (show APP Antibodies)-mediated mitochondrial fragmentation and dysfunction in AD.
the mortalin/DJ-1 (show PARK7 Antibodies) complex guards against mitochondrial oxidative stress and is indispensable for the maintenance of hematopoietic stem cells
Inflammatory response of microglial cells includes a glycolytic shift and is modulated by mitochondrial glucose-regulated protein (show HSP90B1 Antibodies) 75/mortalin.
Knockdown of Hspa9 results in a decrease in hematopoietic progenitors resulting in myelodysplastic syndromes.
Data show that RNAi-mediated down-regulation of GRP75 and GRP75-blocking antibodies, both of which inhibited macromolecular endocytosis.
The asymmetric segregation of mortalin in the bipotent cell line and its uniform distribution in a committed, lineage-restricted cell line raises the possibility that it may play a role in cell fate determination
Mortalin imaging was used in normal and cancer cells with quantum dotimmuno-conjugates.
We propose that the differential regulation of mortalin in AD and by the APOE (show APOE Antibodies) genotype is a cellular defense mechanism responding to increases in oxidative stress.
This gene encodes a member of the heat shock protein 70 gene family. The encoded protein is primarily localized to the mitochondria but is also found in the endoplasmic reticulum, plasma membrane and cytoplasmic vesicles. This protein is a heat-shock cognate protein. This protein plays a role in cell proliferation, stress response and maintenance of the mitochondria. A pseudogene of this gene is found on chromosome 2.
heat shock 70kDa protein 9 (mortalin)
, heat shock 70kDa protein 9B
, Stress-70 protein, mitochondrial-like protein
, heat shock 70 kDa protein 9B
, stress-70 protein, mitochondrial
, heat shock 70 kDa protein 9
, 75 kDa glucose-regulated protein
, stress-70 protein, mitochondrial-like
, heat shock 70kD protein 9B
, mortalin, perinuclear
, peptide-binding protein 74
, GRP 75
, heat shock 70kDa protein 9B (mortalin-2)
, C3H-specific antigen
, heat shock protein 9A
, heat shock protein cognate 74
, heat shock protein, 74 kDa, A
, heat shock protein, A
, p66 MOT
, heat shock 70kDa protein 9A
, 70 kDa heat shock protein
, Heat shock 70 kDa protein 9