The stated application concentrations are suggested starting amounts. Titration of the anti-MBP antibody may be required due to differences in protocols and secondary/substrate sensitivity.\. Western blot: 1:5000-1:16000,Immunofluorescence: 1:10-1:50
For Research Use only
In ascites with 0.09 % sodium azide
Precaution of Use
This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
Aliquot the anti-MBP antibody and store frozen at -20°C or colder. Avoid repeated freeze-thaw cycles.
C76307, Hmbpr, R75289, golli-mbp, mld, shi, Mbps, cb274, fj33b11, mbp, wu:fj33b11, wu:fq15b02, zgc:136630, MGC115135, MBP, mMBP, mMBP-1, myelin basic protein, myelin basic protein a, myelin basic protein L homeolog, proteoglycan 2, bone marrow, MBP, Mbp, mbpa, mbp, mbp.L, Prg2
The protein encoded by the classic MBP gene is a major constituent of the myelin sheath of oligodendrocytes and Schwann cells in the nervous system. However, MBP-related transcripts are also present in the bone marrow and the immune system. These mRNAs arise from the long MBP gene (otherwise called 'Golli-MBP') that contains 3 additional exons located upstream of the classic MBP exons. Alternative splicing from the Golli and the MBP transcription start sites gives rise to 2 sets of MBP-related transcripts and gene products. The Golli mRNAs contain 3 exons unique to Golli-MBP, spliced in-frame to 1 or more MBP exons. They encode hybrid proteins that have N-terminal Golli aa sequence linked to MBP aa sequence. The second family of transcripts contain only MBP exons and produce the well characterized myelin basic proteins. This complex gene structure is conserved among species suggesting that the MBP transcription unit is an integral part of the Golli transcription unit and that this arrangement is important for the function and/or regulation of these genes. [provided by RefSeq].