IGLL1 Break Apart FISH Probe

The preB cell receptor is found on the surface of proB and preB cells, where it is involved in transduction of signals for cellular proliferation, differentiation from the proB cell to the preB cell stage, allelic exclusion at the Ig heavy chain gene locus, and promotion of Ig light chain gene rearrangements. The preB cell receptor is composed of a membrane-bound Ig mu heavy chain in association with a heterodimeric surrogate light chain. This gene encodes one of the surrogate light chain subunits and is a member of the immunoglobulin gene superfamily. This gene does not undergo rearrangement. Mutations in this gene can result in B cell deficiency and agammaglobulinemia, an autosomal recessive disease in which few or no gamma globulins or antibodies are made. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]


Gene Details
SKU Test Kits Buffer Dye Color Order Now
IGLL1BA-20-REGO 20 (40 μL) 200 μL color color Request Pricing
IGLL1BA-20-REGR 20 (40 μL) 200 μL color color Request Pricing
IGLL1BA-20-ORGR 20 (40 μL) 200 μL color color Request Pricing
IGLL1BA-20-GOGR 20 (40 μL) 200 μL color color Request Pricing
IGLL1BA-20-GRRE 20 (40 μL) 200 μL color color Request Pricing
IGLL1BA-20-GROR 20 (40 μL) 200 μL color color Request Pricing
IGLL1BA-20-GRGO 20 (40 μL) 200 μL color color Request Pricing
IGLL1BA-20-AQOR 20 (40 μL) 200 μL color color Request Pricing

Gene Summary

The preB cell receptor is found on the surface of proB and preB cells, where it is involved in transduction of signals for cellular proliferation, differentiation from the proB cell to the preB cell stage, allelic exclusion at the Ig heavy chain gene locus, and promotion of Ig light chain gene rearrangements. The preB cell receptor is composed of a membrane-bound Ig mu heavy chain in association with a heterodimeric surrogate light chain. This gene encodes one of the surrogate light chain subunits and is a member of the immunoglobulin gene superfamily. This gene does not undergo rearrangement. Mutations in this gene can result in B cell deficiency and agammaglobulinemia, an autosomal recessive disease in which few or no gamma globulins or antibodies are made. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]

Gene Details

Gene Symbol : IGLL1

Gene Name : Immunoglobulin lambda like polypeptide 1

Chromosome : CHR 22: 235,805,47-235,731,24

Locus : 22q11.23

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