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Recombinant SREBP-1 Monoclonal Antibody (AN301398L)

Recombinant SREBP-1 Monoclonal Antibody - 1
  • Recombinant SREBP-1 Monoclonal Antibody - 1
  • Recombinant SREBP-1 Monoclonal Antibody - 2
  • Recombinant SREBP-1 Monoclonal Antibody - 3
All Size Price Qty
100μL $ 320.00
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For research use only.

Verified Samples Verified Samples in IHC: Human lung cancer, Rat spleen
Dilution IHC 1:200-1:1000
Isotype IgG,κ
Host Rabbit
Reactivity Human,  Mouse,  Rat
Applications WB,  IHC
Clonality Monoclonal;Recombinant
Immunogen Recombinant Human SREBP-1 protein
Abbre SREBP-1
Synonyms BHLHD,  SREBP,  SREBF,  BHLHD1,  SREBP1,  SREBF1
Swissprot
Cellular Localization Endoplasmic reticulum membrane, Multi-pass membrane protein, Golgi apparatus membrane, Multi-pass membrane protein, Cytoplasmic vesicle, COPII-coated vesicle membrane, Multi-pass membrane protein, At high sterol concentrations, the SCAP-SREBP is retained in the endoplasmic reticulum. Low sterol concentrations promote recruitment into COPII-coated vesicles and transport of the SCAP-SREBP to the Golgi, where it is processed, Nucleus, Nucleus, Nucleus.
Concentration 0.2 mg/mL
Buffer PBS, 50% glycerol, 0.05% Proclin 300, 0.05% protein protectant.
Purification Method Protein A
Research Areas Cardiovascular,  Epigenetics and Nuclear Signaling,  Cancer,  Metabolism
Clone No. 11A12
Conjugation Unconjugated
Storage Store at -20°C Valid for 12 months. Avoid freeze / thaw cycles.
Shipping Ice bag
background This gene encodes a transcription factor that binds to the sterol regulatory element-1 (SRE1), which is a decamer flanking the low density lipoprotein receptor gene and some genes involved in sterol biosynthesis. The protein is synthesized as a precursor that is attached to the nuclear membrane and endoplasmic reticulum. Following cleavage, the mature protein translocates to the nucleus and activates transcription by binding to the SRE1. Sterols inhibit the cleavage of the precursor, and the mature nuclear form is rapidly catabolized, thereby reducing transcription. The protein is a member of the basic helix-loop-helix-leucine zipper (bHLH-Zip) transcription factor family. This gene is located within the Smith-Magenis syndrome region on chromosome 17.
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Unconjugated

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