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ABCG8 Antibody [DyLight 550] 0.1ml

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More on This Product

  • ABCG8 Primary Antibodies
  • All ABCG8 Products
  • Alternate Names
     
  • Pathways & Diseases
  • Bioinformatics Tool

Ordering Information

Catalog Number  NB400-110R
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  • Size(s)0.1ml
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ABCG8 Antibody [DyLight 550] Summary
 
Species Human, Mouse (Negative)
Tested Applications WB
Clonality Polyclonal
Host Rabbit
Gene ABCG8
Purity Immunogen affinity purified
Specificity Specific for ABCG8.
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ABCG8 Antibody [DyLight 550] Details
 
Conjugate DyLight 550 (A=562, E=576)
Immunogen A synthetic peptide from the N-terminal region of human ABCG8 protein.
Localization Integral membrane protein; multi-pass membrane protein
Applications/Dilutions
 
Dilutions
  • Western Blot 1:500
Application Notes

It does not appear to be applicable in immunohistochemistry.

Directly Conjugated
Formats
DyLight 488 Labeled NB400-110G
DyLight 650 Labeled NB400-110C
Biotin Labeled NB400-110B
HRP Labeled NB400-110H
Learn about Custom Antibody Labeling
Product PDFs
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Publications
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Controls & Support Products
Research Tools
View all ABCG8 Research Tools.
Packaging, Storage & Formulations
 
Storage Store at 4C in the dark.
Buffer 50mM sodium borate
Unit Size 0.1ml
Concentration 1.0 mg/ml
Preservative No Preservative
Limitations This product is for research use only and is not approved for use in humans or in clinical diagnosis. Products are guaranteed for 6 months from date of receipt.
Bioinformatics
 
Gene Symbol ABCG8
Entrez
Uniprot
Alternate Names for ABCG8
 
  • ATP-binding cassette sub-family G member 8
  • ATP-binding cassette
  • sub-family G (WHITE)
  • member
  • ATP-binding cassette
  • sub-family G (WHITE)
  • member
  • GBD4ATP-binding cassette
  • subfamily G
  • member 8 sl
  • MGC142217
  • sterolin 2
  • sterolin-2
  • Sterolin-2
  • STSL
Related Products by Gene
Background
 
ATP-binding cassette (ABC) transporter genes are involved in the regulation of the amount of dietary cholesterol retained in the body. ABCG8, expressed at high levels in the liver and intestine, normally cooperates with ABCG5 to limit intestinal absorption and promote biliary excretion of sterols. The mutated form of this transporter can lead to sterol accumulation and atherosclerosis or sitosterolemia, a rare autosomal recessive disorder, characterized by hyperabsorption of sterols and the inability to excrete sterols into bile.