名称：NSDHL

别名：H105E3; XAP104; SDR31E1

Targets：Disease

描述

The protein encoded by this gene is localized in the endoplasmic reticulum and is involved in cholesterol biosynthesis. Mutations in this gene are associated with CHILD syndrome, which is a X-linked dominant disorder of lipid metabolism with disturbed cholesterol biosynthesis, and typically lethal in males. Alternatively spliced transcript variants with differing 5' UTR have been found for this gene.

Specification

Entrez GeneID：50814

Swissprot：Q15738

WB Predicted band size：Calculated MW: 42 kDa; Observed MW: 42 kDa

Host/Isotype：Rabbit IgG

Antibody Type：Primary antibody

Storage：Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze/thaw cycles.

Species Reactivity：Human

免疫原：A synthetic peptide of human NSDHL

Formulation：Purified antibody in TBS with 0.05% sodium azide,0.05%BSA and 50% glycerol.

Application

Application：WB,IP

WB：1/500-1/1000

IP：1/10-1/20

宿主：Rabbit