NSDHL Antibody (SR1643) - BSA Free

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Western Blot: NSDHL Antibody (SR1643) [NBP3-22589] - Western blot analysis using NBP3-22589 in A431 cell lysate.

Product Details

Summary
Reactivity HuSpecies Glossary
Applications WB, ICC/IF, IHC
Clone
SR1643
Clonality
Monoclonal
Host
Rabbit
Conjugate
Unconjugated
Format
BSA Free

Order Details

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Catalog# & Formulation Size Price

NSDHL Antibody (SR1643) - BSA Free Summary

Description
Novus Biologicals Rabbit NSDHL Antibody (SR1643) - BSA Free (NBP3-22589) is a recombinant monoclonal antibody validated for use in IHC, WB and ICC/IF. All Novus Biologicals antibodies are covered by our 100% guarantee.
Additional Information
Recombinant Monoclonal Antibody
Immunogen
A synthesized peptide derived from human NSDHL (Uniprot #: Q15738)
Specificity
Detects endogenous levels of total NSDHL
Source
HEK293
Isotype
IgG
Clonality
Monoclonal
Host
Rabbit
Gene
NSDHL
Purity
Affinity purified
Innovator's Reward
Test in a species/application not listed above to receive a full credit towards a future purchase.

Applications/Dilutions

Dilutions
  • Immunocytochemistry/ Immunofluorescence 1:50-1:200
  • Immunohistochemistry 1:50-1:200
  • Western Blot 1:500-1:2000
Theoretical MW
38 kDa.
Disclaimer note: The observed molecular weight of the protein may vary from the listed predicted molecular weight due to post translational modifications, post translation cleavages, relative charges, and other experimental factors.

Packaging, Storage & Formulations

Storage
Store at 4C short term. Aliquot and store at -20C long term. Avoid freeze-thaw cycles.
Buffer
PBS, pH 7.4, 150mM NaCl, 50% glycerol.
Preservative
0.02% Sodium Azide
Purity
Affinity purified

Alternate Names for NSDHL Antibody (SR1643) - BSA Free

  • EC 1.1.1.170
  • H105e3
  • member 1
  • NAD(P) dependent steroid dehydrogenase-like
  • SDR31E1
  • sterol-4-alpha-carboxylate 3-dehydrogenase, decarboxylating
  • XAP104

Background

NSDHL is 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. [provided by RefSeq]

Limitations

This product is for research use only and is not approved for use in humans or in clinical diagnosis. Primary Antibodies are guaranteed for 1 year from date of receipt.

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Product General Protocols

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Video Protocols

WB Video Protocol
ICC/IF Video Protocol

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Bioinformatics

Gene Symbol NSDHL