HSP27 Mouse Monoclonal Antibody
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AMM3315-61 50ul 1500.00 In Stock
AMM3315-61 100ul 2000.00 In Stock
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Source: Mouse Gene Id: 3315
Isotype: IgG1 Swiss Prot: P04792
purity: Affinity chromatography
Background:
The protein encoded by this gene is induced by environmental stress and developmental changes. The encoded protein is involved in stress resistance and actin organization and translocates from the cytoplasm to the nucleus upon stress induction. Defects in this gene are a cause of Charcot-Marie-Tooth disease type 2F (CMT2F) and distal hereditary motor neuropathy (dHMN). (provided by RefSeq) 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.
Reactivity Human, Rat
Tested applications WB IHC ELISA ICC FC
Clonality Monoclonal Antibody
Calculated MW 27 kDa
Recommended Dilutions
WB 1:500-1:2000
IHC 1:200-1:1000
ICC 1:200-1:1000
FC 1:200-1:400
Immunogen A purified recombinant fragment of human HSP27 expressed in E. Coli
Storage Store at -20°C or -80°C in PBS with 0.02% sodium azide and 50% glycerol. Avoid freeze/thaw cycles.
Synonym CMT2F, HMN2B, HSP27, HSP28, Hsp25, SRP27, HS.76067, DKFZp586P1322, HSPB1
This product is for research use only, not for diagnostic or therapeutic use!

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