LMAN1 Break Apart FISH Probe

The protein encoded by this gene is a membrane mannose-specific lectin that cycles between the endoplasmic reticulum, endoplasmic reticulum-Golgi intermediate compartment, and cis-Golgi, functioning as a cargo receptor for glycoprotein transport. The protein has an N-terminal signal sequence, a calcium-dependent and pH-sensitive carbohydrate recognition domain, a stalk region that functions in oligomerization, a transmembrane domain, and a short cytoplasmic domain required for organelle targeting. Allelic variants of this gene are associated with the autosomal recessive disorder combined factor V-factor VIII deficiency. [provided by RefSeq, Jul 2015]


Gene Details
SKU Test Kits Buffer Dye Color Order Now
LMAN1BA-20-REGO 20 (40 μL) 200 μL color color Request Pricing
LMAN1BA-20-REGR 20 (40 μL) 200 μL color color Request Pricing
LMAN1BA-20-ORGR 20 (40 μL) 200 μL color color Request Pricing
LMAN1BA-20-GOGR 20 (40 μL) 200 μL color color Request Pricing
LMAN1BA-20-GRRE 20 (40 μL) 200 μL color color Request Pricing
LMAN1BA-20-GROR 20 (40 μL) 200 μL color color Request Pricing
LMAN1BA-20-GRGO 20 (40 μL) 200 μL color color Request Pricing
LMAN1BA-20-AQOR 20 (40 μL) 200 μL color color Request Pricing

Gene Summary

The protein encoded by this gene is a membrane mannose-specific lectin that cycles between the endoplasmic reticulum, endoplasmic reticulum-Golgi intermediate compartment, and cis-Golgi, functioning as a cargo receptor for glycoprotein transport. The protein has an N-terminal signal sequence, a calcium-dependent and pH-sensitive carbohydrate recognition domain, a stalk region that functions in oligomerization, a transmembrane domain, and a short cytoplasmic domain required for organelle targeting. Allelic variants of this gene are associated with the autosomal recessive disorder combined factor V-factor VIII deficiency. [provided by RefSeq, Jul 2015]

Gene Details

Gene Symbol : LMAN1

Gene Name : Lectin, mannose binding 1

Chromosome : CHR 18: 593,592,75-593,278,22

Locus : 18q21.32

Alt. Genes : FEM1B

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