Seracare Fmr1
Lab Reagents
Human IgG antibody Laboratories manufactures the seracare fmr1 reagents distributed by Genprice. The Seracare Fmr1 reagent is RUO (Research Use Only) to test human serum or cell culture lab samples. To purchase these products, for the MSDS, Data Sheet, protocol, storage conditions/temperature or for the concentration, please contact SeraCare Inc.. Other Seracare products are available in stock. Specificity: Seracare Category: Fmr1
FMR1 antibody |
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10R-6945 | Fitzgerald | 100 ul | EUR 726 |
Description: Mouse monoclonal FMR1 antibody |
FMR1 antibody |
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10R-6946 | Fitzgerald | 100 ul | EUR 691 |
Description: Mouse monoclonal FMR1 antibody |
FMR1 antibody |
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10R-6947 | Fitzgerald | 100 ul | EUR 691 |
Description: Mouse monoclonal FMR1 antibody |
Fmr1 antibody |
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70R-8477 | Fitzgerald | 50 ug | EUR 467 |
Description: Affinity purified rabbit polyclonal Fmr1 antibody |
FMR1 Peptide |
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46-842P | ProSci | 0.1 mg | EUR 338 |
Description: FMR1 Peptide |
FMR1 Peptide |
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7707P | ProSci | 0.05 mg | EUR 164.75 |
Description: (CT) FMR1 Peptide |
FMR1 Peptide |
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42-001P | ProSci | 0.1 mg | EUR 338 |
Description: FMR1 (aa116-130) Peptide |
FMR1 Antibody |
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7707-002mg | ProSci | 0.02 mg | EUR 171.82 |
Description: Fragile X syndrome is a frequent form of inherited mental retardation caused by functional loss of the fragile X mental retardation protein, FMR1, also known as FMRP (1). FMR1 binds RNA and is associated with polysomes. The encoded protein may be involved in mRNA trafficking from the nucleus to the cytoplasm (2). A trinucleotide repeat (CGG) in the 5' UTR is normally found at 6-53 copies, but an expansion to 55-230 repeats is the cause of fragile X syndrome (1). Expansion of the trinucleotide repeat may also cause one form of premature ovarian failure (POF1) (3). |
FMR1 Antibody |
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7707-01mg | ProSci | 0.1 mg | EUR 436.42 |
Description: Fragile X syndrome is a frequent form of inherited mental retardation caused by functional loss of the fragile X mental retardation protein, FMR1, also known as FMRP (1). FMR1 binds RNA and is associated with polysomes. The encoded protein may be involved in mRNA trafficking from the nucleus to the cytoplasm (2). A trinucleotide repeat (CGG) in the 5' UTR is normally found at 6-53 copies, but an expansion to 55-230 repeats is the cause of fragile X syndrome (1). Expansion of the trinucleotide repeat may also cause one form of premature ovarian failure (POF1) (3). |
FMR1 Rabbit pAb |
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A5645-100ul | Abclonal | 100 ul | EUR 308 |
FMR1 Rabbit pAb |
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A5645-200ul | Abclonal | 200 ul | EUR 459 |
FMR1 Rabbit pAb |
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A5645-20ul | Abclonal | 20 ul | EUR 183 |
FMR1 Rabbit pAb |
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A5645-50ul | Abclonal | 50 ul | EUR 223 |
FMR1 Rabbit pAb |
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A6092-100ul | Abclonal | 100 ul | EUR 308 |
FMR1 Rabbit pAb |
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A6092-200ul | Abclonal | 200 ul | EUR 459 |
FMR1 Rabbit pAb |
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A6092-20ul | Abclonal | 20 ul | EUR 183 |
FMR1 Rabbit pAb |
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A6092-50ul | Abclonal | 50 ul | EUR 223 |