Product Detail
Product NameAlbumin Rabbit mAb
Clone No.JF32-10
Host SpeciesRecombinant Rabbit
ClonalityMonoclonal
PurificationProA affinity purified
ApplicationsWB, IHC
Species ReactivityHu, Ms, Rt, Cow
Immunogen Descrecombinant protein
ConjugateUnconjugated
Other Namesalb antibody ALBU_HUMAN antibody Albumin (32 AA) antibody Albumin (AA 34) antibody cell growth inhibiting protein 42 antibody DKFZp779N1935 antibody GIG20 antibody GIG42 antibody growth-inhibiting protein 20 antibody OTTHUMP00000220436 antibody OTTHUMP00000220438 antibody OTTHUMP00000220439 antibody PRO0883 antibody PRO0903 antibody PRO1341 antibody PRO1708 antibody PRO2044 antibody PRO2619 antibody PRO2675 antibody Serum albumin antibody UNQ696/PRO1341 antibody
Accession NoSwiss-Prot#:P02768
Uniprot
P02768
Gene ID
213;
Calculated MW69 kDa
Formulation1*TBS (pH7.4), 1%BSA, 40%Glycerol. Preservative: 0.05% Sodium Azide.
StorageStore at -20˚C
Application Details
WB: 1:1,000-5,000
IHC: 1:50-1:200
Western blot analysis of Albumin on Hela cells lysates using anti-Albumin antibody at 1/1,000 dilution.
Immunohistochemical analysis of paraffin-embedded human lung tissue using anti-Albumin antibody. Counter stained with hematoxylin.
Immunohistochemical analysis of paraffin-embedded human liver tissue using anti-Albumin antibody. Counter stained with hematoxylin.
Immunohistochemical analysis of paraffin-embedded human spleen tissue using anti-Albumin antibody. Counter stained with hematoxylin.
Immunohistochemical analysis of paraffin-embedded mouse lung tissue using anti-Albumin antibody. Counter stained with hematoxylin.
Immunohistochemical analysis of paraffin-embedded human kidney tissue using anti-Albumin antibody. Counter stained with hematoxylin.
Immunohistochemical analysis of paraffin-embedded mouse liver tissue using anti-Albumin antibody. Counter stained with hematoxylin.
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.
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