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Mouse Monoclonal HSP27 antibody [5D7] (STJ98141)
Supplier: St John’s Laboratory Ltd.
Recommended applications: WB, IHC, IF, FC, ELISA
Recommended dilution: WB 1:500-1:2000; IHC 1:200-1:1000; IF 1:200-1:1000; FC 1:200-1:400; ELISA 1:10000
Recommended protocols: check protocols
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Check alternative names for the antibodyExpand
HSPB1 antibody, HSP27 antibody, HSP28 antibody,|Heat shock 27kDa protein antibody|28 kDa heat shock protein antibody|CMT2F antibody|DKFZp586P1322 antibody|epididymis secretory protein Li 102 antibody|Estrogen regulated 24 kDa protein antibody|Estrogen-regulated 24 kDa protein antibody|Heat shock 25kDa protein 1 antibody|Heat shock 27 kDa protein antibody|Heat shock 27kD protein 1 antibody|Heat shock 27kDa protein 1 antibody|Heat shock 28kDa protein 1 antibody|Heat Shock Protein 27 antibody|Heat shock protein beta 1 antibody|Heat shock protein beta-1 antibody|heat shock protein family B (small) member 1 antibody|HEL-S-102 antibody|HMN2B antibody|HS.76067 antibody|Hsp 25 antibody|HSP 27 antibody|Hsp 28 antibody|Hsp B1 antibody|Hsp25 antibody|HSP27 antibody|Hsp28 antibody|HspB1 antibody|HSPB1_HUMAN antibody|SRP27 antibody|Stress responsive protein 27 antibody|Stress-responsive protein 27 antibody|Anti-Hsp27 antibody [G3.1] (ab2790)
SCBT cat No: sc-1048|sc-13132|sc-59562|sc-9012|sc-51956|sc-51958|sc-1049|sc-135943|sc-398766|sc-1800|sc-28845|sc-1801|sc-376544|sc-47051|sc-135152|
HSP27 Monoclonal Antibody
|Catalogue No.|| |
HSP27 Monoclonal Antibody detects endogenous levels of HSP27 protein.
Purified recombinant fragment of human HSP27 expressed in E Coli
WB, IHC, IF, FC, ELISA
|Recommended dilution|| |
WB 1:500-1:2000; IHC 1:200-1:1000; IF 1:200-1:1000; FC 1:200-1:400; ELISA 1:10000
HSP27 Antibody was tube-contained. Ascitic fluid containing 0.03% sodium azide.
HSP27 Antibody was purified using affinity purification.
-20 Celsius degree. Avoid repeated freeze/thaw cycles.
|Alternative antibody names|| |
Heat shock protein beta-1 antibody, HspB1 antibody, 28 kDa heat shock protein antibody, Estrogen-regulated 24 kDa protein antibody, Heat shock 27 kDa protein antibody, HSP 27 antibody, Stress-responsive protein 27 antibody, SRP27 antibody
|Protein names|| |
Heat shock protein beta-1 , HspB1 , 28 kDa heat shock protein , Estrogen-regulated 24 kDa protein , Heat shock 27 kDa protein , HSP 27 , Stress-responsive protein 27 , SRP27
|Protein function|| |
Involved in stress resistance and actin organization.
|Protein tissue specificity|| |
Detected in all tissues tested: skeletal muscle, heart, aorta, large intestine, small intestine, stomach, esophagus, bladder, adrenal gland, thyroid, pancreas, testis, adipose tissue, kidney, liver, spleen, cerebral cortex, blood serum and cerebrospinal fluid. Highest levels are found in the heart and in tissues composed of striated and smooth muscle.
|Involvement in disease|| |
Charcot-Marie-Tooth disease 2F (CMT2F) [MIM:606595]: A dominant axonal form of Charcot-Marie-Tooth disease, a disorder of the peripheral nervous system, characterized by progressive weakness and atrophy, initially of the peroneal muscles and later of the distal muscles of the arms. Charcot-Marie-Tooth disease is classified in two main groups on the basis of electrophysiologic properties and histopathology: primary peripheral demyelinating neuropathies (designated CMT1 when they are dominantly inherited) and primary peripheral axonal neuropathies (CMT2). Neuropathies of the CMT2 group are characterized by signs of axonal degeneration in the absence of obvious myelin alterations, normal or slightly reduced nerve conduction velocities, and progressive distal muscle weakness and atrophy. Nerve conduction velocities are normal or slightly reduced. Onset of Charcot-Marie-Tooth disease type 2F is between 15 and 25 years with muscle weakness and atrophy usually beginning in feet and legs (peroneal distribution). Upper limb involvement occurs later. . Note: The disease is caused by mutations affecting the gene represented in this entry.; Neuronopathy, distal hereditary motor, 2B (HMN2B) [MIM:608634]: A neuromuscular disorder. Distal hereditary motor neuronopathies constitute a heterogeneous group of neuromuscular disorders caused by selective degeneration of motor neurons in the anterior horn of the spinal cord, without sensory deficit in the posterior horn. The overall clinical picture consists of a classical distal muscular atrophy syndrome in the legs without clinical sensory loss. The disease starts with weakness and wasting of distal muscles of the anterior tibial and peroneal compartments of the legs. Later on, weakness and atrophy may expand to the proximal muscles of the lower limbs and/or to the distal upper limbs. . Note: The disease is caused by mutations affecting the gene represented in this entry.
|Protein sequence and domain|| |
Belongs to the small heat shock protein (HSP20) family.
|Protein post-translational modifications|| |
Phosphorylated in MCF-7 cells on exposure to protein kinase C activators and heat shock. / Phosphorylation by MAPKAPK2 and MAPKAPK3 in response to stress leads to dissociate HSP27/HSPB1 from large small heat-shock protein (sHsps) oligomers and impair its chaperone activity and ability to protect against oxidative stress effectively. Phosphorylation by MAPKAPK5 in response to PKA stimulation induces F-actin rearrangement.
|Protein cellular localization|| |
Cytoplasm / Nucleus / Cytoplasm > cytoskeleton > spindle
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St John’s Laboratory Ltd.
|Product type|| |
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