DATASHEET
Host:
Rabbit
Target Protein:
phospho-MBP (Thr232)
Specificity:
This antibody recognizes Thr229 in mice and Thr122 in rat
Modification Site:
Thr232
Clonality:
Polyclonal
Isotype:
IgG
Entrez Gene:
4155
Swiss Prot:
P02686
Source:
KLH conjugated synthetic phosphopeptide derived from human MBP around the phosphorylation site of Thr232
Purification:
Purified by Protein A.
Storage Buffer:
0.01M TBS(pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.
Storage:
Shipped at 4℃. Store at -20℃ for one year. Avoid repeated freeze/thaw cycles.
Background:
The classic group of MBP isoforms (isoform 4-isoform 14) are with PLP the most abundant protein components of the myelin membrane in the CNS. They have a role in both its formation and stabilization. The smaller isoforms might have an important role in remyelination of denuded axons in multiple sclerosis. The non-classic group of MBP isoforms (isoform 1-isoform 3/Golli-MBPs) may preferentially have a role in the early developing brain long before myelination, maybe as components of transcriptional complexes, and may also be involved in signaling pathways in T-cells and neural cells. Differential splicing events combined with optional post-translational modifications give a wide spectrum of isomers, with each of them potentially having a specialized function. Induces T-cell proliferation.
VALIDATION IMAGES
Formalin-fixed and paraffin embedded rat brain labeled with Anti-phospho-MBP(Thr232)Polyclonal Antibody, Unconjugated (bs-5474R) at 1:200 followed by conjugation to the secondary antibody and DAB staining\n
U-937 cells were incubated in 5% BSA blocking buffer for 30 min at room temperature. Cells were then stained with MBP(Thr232) Polyclonal Antibody(bs-5474R)at 1:100 dilution in blocking buffer and incubated for 30 min at room temperature, washed twice with 2%BSA in PBS, followed by secondary antibody incubation for 40 min at room temperature. Acquisitions of 20,000 events were performed. Cells stained with primary antibody (green), and isotype control (orange).