Anti-NSDHL Rabbit Monoclonal Antibody
Catalog No.
MA4049
Anti-NSDHL Rabbit Monoclonal Antibody
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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.
50814
H105E3; XAP104; SDR31E1
Rabbit
Human
Unconjugated
Calculated MW: 42 kDa; Observed MW: 42 kDa
Unmodified
IgG
Monoclonal Antibody
AP-2B7C8
Liquid
See label
Carrier Not Free
A synthetic peptide of human NSDHL
Affinity Purified
50mM Tris-Glycine (pH 7.4), 0.15M NaCl, 40% Glycerol, 0.01% Sodium azide and 0.05% BSA.
WB, IP
Blue ice
-20°C
12 months
Please avoid freeze-thaw cycles.