Anti-Ceramide synthase 2 antibody (ab81253)

Overview

  • Product nameAnti-Ceramide synthase 2 antibody
    See all Ceramide synthase 2 primary antibodies
  • Description
    Rabbit polyclonal to Ceramide synthase 2
  • Tested applicationsSuitable for: WBmore details
  • Species reactivity
    Reacts with: Human
  • Immunogen

    Synthetic peptide derived from human LASS2 protein

  • Positive control
    • Liver and Kidney. Human placenta lysate

Properties

Associated products

Applications

Our Abpromise guarantee covers the use of ab81253 in the following tested applications.

The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.

Application Abreviews Notes
WB Use a concentration of 1 - 5 µg/ml. Predicted molecular weight: 45 kDa.

Target

  • FunctionSuppresses the growth of cancer cells. May be involved in sphingolipid synthesis.
  • Tissue specificityExpressed in kidney, liver, brain, heart, placenta and lung.
  • Sequence similaritiesContains 1 homeobox DNA-binding domain.
    Contains 1 TLC (TRAM/LAG1/CLN8) domain.
  • Cellular localizationNucleus membrane. Endoplasmic reticulum membrane.
  • Information by UniProt
  • Database links
  • Alternative names
    • Ceramide synthase 2 antibody
    • CerS 2 antibody
    • CerS2 antibody
    • CERS2_HUMAN antibody
    • FLJ10243 antibody
    • L3 antibody
    • LAG1 homolog ceramide synthase 2 antibody
    • LAG1 longevity assurance 2 antibody
    • LAG1 longevity assurance homolog 2 antibody
    • LASS 2 antibody
    • Longevity assurance (LAG1 S. cerevisiae) homolog 2 antibody
    • MGC987 antibody
    • SP 260 antibody
    • SP260 antibody
    • TMSG 1 antibody
    • TMSG1 antibody
    • Tumor metastasis suppressor antibody
    • Tumor metastasis suppressor gene 1 protein antibody
    • Tumor metastasis-suppressor gene 1 protein antibody
    see all

References for Anti-Ceramide synthase 2 antibody (ab81253)

ab81253 has not yet been referenced specifically in any publications.

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