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ALB (BGN/1328/33) Antibody: sc-80674

 |  Datasheet
  • mouse monoclonal IgG1, 100µg/ml
  • raised against native ALB of human origin
  • recommended for detection of ALB of human origin by WB and IP
 
Additional Albumin Antibodies ...
 
Ordering Information
Recommended Support Products:
(click button of application of choice)
WB   IP   siRNA  
 
Species Gene Name Gene ID Chromosome Location Isoform (mRNA) Accession # Protein Accession # OMIM™ Number
Human ALB 213 4q13.3 NM_000477 P02768
194470
 
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 Ordering Information
Product NameCatalog #UnitPriceQtyAddFavorites
ALB (BGN/1328/33) sc-80674 100 µg/ml $279
 siRNA Gene Silencers (click product name for more information)
Product NameCatalog #UnitPriceQtyAddFavorites
ALB siRNA (h) sc-45606 10 µM $258
ALB siRNA (h)-PR sc-45606-PR 10 µM $23
 shRNA Plasmids (click product name for more information)
Product NameCatalog #UnitPriceQtyAddFavorites
ALB shRNA Plasmid (h) sc-45606-SH 20 µg $520
 shRNA Lentiviral Particles (click product name for more information)
Product NameCatalog #UnitPriceQtyAddFavorites
ALB siRNA shRNA (h) Lentiviral Particles sc-45606-V 200 µl $625
 WB Positive Control Cell Lysates (click product name for more information)
Product NameCatalog #UnitPriceQtyAddFavorites
Hep G2 Cell Lysate sc-2227 500 µg/200 µl $104
HeLa Whole Cell Lysate sc-2200 500 µg/200 µl $104

ALB Background Information
Serum albumin (ALB), the main protein in plasma, has a very good binding capacity for water, fatty acids, calcium, sodium, bilirubin, hormones, potassium and drugs. The primary function of ALB is to regulate the colloidal osmotic pressure of blood. Albumin is synthesized in the liver as preproalbumin, which has an N-terminal peptide that is removed before the nascent protein is released from the rough endoplasmic reticulum. The product, proalbumin, is in turn cleaved in the Golgi vesicles to produce the secreted form of albumin. Mutations in the ALB gene may result in familial dysalbuminemic hyperthyroxinemia (FDH), a form of euthyroid hyperthyroxinemia that is due to increased affinity of ALB for T4. FDH is the most common cause of inherited euthyroid hyperthyroxinemia in Caucasian populations.

ALB (BGN/1328/33)
Click on image to enlarge
ALB (BGN/1328/33): sc-80674. Western blot analysis of ALB expression in human PBL whole cell lysate.
ALB (BGN/1328/33): sc-80674. Western blot analysis of ALB expression in Hep G2 whole cell lysate.
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