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

Serum / Plasma information

FMR1 antibody

10R-6945 100 ul
EUR 726
Description: Mouse monoclonal FMR1 antibody

FMR1 antibody

10R-6946 100 ul
EUR 691
Description: Mouse monoclonal FMR1 antibody

FMR1 antibody

10R-6947 100 ul
EUR 691
Description: Mouse monoclonal FMR1 antibody

Fmr1 antibody

70R-8477 50 ug
EUR 467
Description: Affinity purified rabbit polyclonal Fmr1 antibody

FMR1 Peptide

46-842P 0.1 mg
EUR 338
Description: FMR1 Peptide

FMR1 Peptide

7707P 0.05 mg
EUR 164.75
Description: (CT) FMR1 Peptide

FMR1 Peptide

42-001P 0.1 mg
EUR 338
Description: FMR1 (aa116-130) Peptide

FMR1 Antibody

7707-002mg 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

7707-01mg 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

A5645-100ul 100 ul
EUR 308

FMR1 Rabbit pAb

A5645-200ul 200 ul
EUR 459

FMR1 Rabbit pAb

A5645-20ul 20 ul
EUR 183

FMR1 Rabbit pAb

A5645-50ul 50 ul
EUR 223

FMR1 Rabbit pAb

A6092-100ul 100 ul
EUR 308

FMR1 Rabbit pAb

A6092-200ul 200 ul
EUR 459

FMR1 Rabbit pAb

A6092-20ul 20 ul
EUR 183

FMR1 Rabbit pAb

A6092-50ul 50 ul
EUR 223