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ALB Anticuerpo(F-10): sc-271605

 |  Ficha Técnica

(Basado en el análisis de datos)

  • ALB Antibody (F-10) is a mouse monoclonal IgG1 provided at 200 µg/ml
  • raised against amino acids 39-164 mapping near the N-terminus of serum albumin of human origin
  • recommended for detection of ALB of human and rat origin by WB, IP, IF, IHC(P) and ELISA
 
Secuencia completa de la proteína para ALB con inmunógeno inidcado:
MKWVTFISLLFLFSSAYSRGVFRRDAHKSEVAHRFKDLGEENFKALVLIAFAQYLQQCPFEDHVKLVNEVTEFAKTCVADESAENCDKSLHTLFGDKLCTVATLRETYGEMADCCAKQEPERNECFLQHKDDNPNLPRLVRPEVDVMCTAFHDNEETFLKKYLYEIARRHPYFYAPELLFFAKRYKAAFTECCQAADKAACLLPKLDELRDEGKASSAKQRLKCASLQKFGERAFKAWAVARLSQRFPKAEFAEVSKLVTDLTKVHTECCHGDLLECADDRADLAKYICENQDSISSKLKECCEKPLLEKSHCIAEVENDEMPADLPSLAADFVESKDVCKNYAEAKDVFLGMFLYEYARRHPDYSVVLLLRLAKTYETTLEKCCAAADPHECYAKVFDEFKPLVEEPQNLIKQNCELFEQLGEYKFQNALLVRYTKKVPQVSTPTLVEVSRNLGKVGSKCCKHPEAKRMPCAEDYLSVVLNQLCVLHEKTPVSDRVTKCCTESLVNRRPCFSALEVDETYVPKEFNAETFTFHADICTLSEKERQIKKQTALVELVKHKPKATKEQLKAVMDDFAAFVEKCCKADDKETCFAEEGKKLVAASQAALGL

Ver tambiénAlbumin AntibodiesincluyebdoAlbumin, ALByBSA.

Información sobre pedidosInformación del gen
Productos Complementarios Recomendados:
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WB   IP   IF   IHC(P)  
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 Información sobre pedidos
Nombre del productoNúmero de catálogoUnidadPrecioCantidadAñadir 
ALB Antibody (F-10) sc-271605 200 µg/ml $279
 
Especies Nombre del Gen Gene ID Ubicación en el cromosoma Numero de Acceso de Isoforma (ARNm) Número de Acceso de la Proteína Número OMIM™:
Humano ALB 213 4q13.3 NM_000477 NP_000468
194470
 


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 Antibody (F-10) Data
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ALB (F-10): sc-271605. Western blot analysis of ALB expression in rat liver tissue extract (A) and Hep G2 whole cell lysate (B).
ALB (F-10): sc-271605. Immunoperoxidase staining of formalin fixed, paraffin-embedded human lung tissue showing membrane and cytoplasmic staining of pneumocytes and macrophages.
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