Product Pathways - Lymphocyte Signaling
RAG1 (D36B3) Rabbit mAb #3968
|3968S||100 µl (10 western blots)||---||In Stock||---|
|3968||carrier free and custom formulation / quantity||email request|
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Species cross-reactivity is determined by western blot.
Applications Key: W=Western Blotting, IP=Immunoprecipitation
Specificity / Sensitivity
RAG1 (D36B3) Rabbit mAb detects endogenous levels of total RAG1 protein.
Source / Purification
Monoclonal antibody is produced by immunizing animals with recombinant human RAG1 protein.
The sequences encoding antigen receptors are split into multiple germline segments which are then combined by a process called V(D)J recombination during immune cells development. A variable (V) segment is combined with a joining (J) segment, and in some cases a D (Diversity) segment, to create the antigen-binding portion of the receptor. The recombined V(D)J segment is then spliced into exons that encode the constant region to produce mature mRNA (1,2). This essential process required for the development of functional immune T and B cells creates a vast diversity in these receptors (3,4). Initiation of this process follows binding of RAG1 (recombination activating gene 1) and RAG2 to the conserved recombination signal sequences (RSS) and the introduction of a double-strand break between the RSS and the coding sequence (5,6). RAG1 and RAG2 genes are located immediately adjacent to each other in the genome and lack introns in their coding regions in many species. RAG1 and RAG2 are coexpressed only in the B and T cell lineages and both are required for cleavage activity (7). RAG1 and RAG2 can also function as transposases, contributing to chromosomal translocations and lymphoid malignancy (8,9). Mutations in the RAG genes are associated with a spectrum of combined immune deficiencies in humans (10,11).
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- Swanson, P.C. et al. (2009) Adv Exp Med Biol 650, 1-15.
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- Agrawal, A. et al. (1998) Nature 394, 744-51.
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For Research Use Only. Not For Use In Diagnostic Procedures.
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