GPD1L (N-term) Rabbit Polyclonal Antibody

CAT#: AP51905PU-N

GPD1L (N-term) rabbit polyclonal antibody, Aff - Purified

Product Images

GPD1L Antibody (N-term) western blot analysis in MCF-7 cell line lysates (35ug/lane).This demonstrates the GPD1L antibody detected the GPD1L protein (arrow).

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  GPD1L Antibody (N-term) western blot analysis in mouse heart tissue lysates (35ug/lane).This demonstrates the GPD1L antibody detected the GPD1L protein (arrow).

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  GPD1L antibody (N-term) immunohistochemistry analysis in formalin fixed and paraffin embedded mouse heart tissue followed by peroxidase conjugation of the secondary antibody and DAB staining. This data demonstrates the use of the GPD1L antibody (N-term) for immunohistochemistry. Clinical relevance has not been evaluated.

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  GPD1L Antibody (N-term) flow cytometric analysis of MCF-7 cells (right histogram) compared to a negative control cell (left histogram).FITC-conjugated goat-anti-rabbit secondary antibodies were used for the analysis.

Specifications

Product Data

• Applications: FC, IHC, WB
• Recommended Dilution: ELISA: 1/1000.
  Western Blot: 1/100 - 1/500.
  Immunohistochemistry on paraffin sections: 1/10 - 1/50.
  Flow Cytometry: 1/10 - 1/50.
• Reactivities: Human, Mouse
• Host: Rabbit
• Isotype: Ig
• Clonality: Polyclonal
• Immunogen: KLH conjugated synthetic peptide between 47-77 amino acids from the N-terminal region of human GPD1L
• Specificity: This antibody reacts to GPD1L.
• Formulation: PBS
  State: Aff - Purified
  State: Liquid purified Ig fraction
  Preservative: 0.09% (W/V) sodium azide
• Concentration: lot specific
• Purification: Affinity chromatography on Protein A
• Conjugation: Unconjugated
• Storage:

  Store the antibody undiluted at 2-8°C for one month or (in aliquots) at -20°C for longer.
  Avoid repeated freezing and thawing.

• Stability: Shelf life: one year from despatch.

• Predicted Protein Size: 38419 Da
• Gene Name: glycerol-3-phosphate dehydrogenase 1-like
• Database Link:
  Entrez Gene 333433 MouseEntrez Gene 23171 Human
  UniProt ID Q8N335
• Background: The protein encoded by this gene catalyzes the conversion of sn-glycerol 3-phosphate to glycerone phosphate. The encoded protein is found in the cytoplasm, associated with the plasma membrane, where it binds the sodium channel, voltage-gated, type V, alpha subunit (SCN5A). Defects in this gene are a cause of Brugada syndrome type 2 (BRS2) as well as sudden infant death syndrome (SIDS).
• Synonyms: KIAA0089, GPD1-L

Reference Data

• Protein Pathways: Glycerophospholipid metabolism