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[KD Validated] SGPL1 Rabbit mAb (A26855)

Datasheet

Tested applications:WBIHC-PIF/ICCIPChIPChIP-seqRIPFCFC(Intra)ELISAMeDIPNucleotide ArrayDBFACSCoIPCUT&TagmeRIPInhibitionReactivity:Human, Mouse, Rat

ABclonal:Western blot - [KD Validated] SGPL1 Rabbit mAb (A26855)

Western blot analysis of lysates from wild type (WT) and SGPL1 knockout (KD) 293T cells using [KD Validated] SGPL1 Rabbit mAb (A26855) at 1:15000 dilution incubated overnight at 4℃.
Secondary antibody: HRP-conjugated Goat anti-Rabbit IgG (H+L) (AS014) at 1:10000 dilution.
Lysates/proteins: 25 μg per lane.
Blocking buffer: 3% nonfat dry milk in TBST.
Detection: ECL Basic Kit (RM00020).
Exposure time: 45s.

ABclonal:Western blot - [KD Validated] SGPL1 Rabbit mAb (A26855)

Western blot analysis of various lysates using [KD Validated] SGPL1 Rabbit mAb (A26855) at 1:15000 dilution incubated overnight at 4℃.
Secondary antibody: HRP-conjugated Goat anti-Rabbit IgG (H+L) (AS014) at 1:10000 dilution.
Lysates/proteins: 25 μg per lane.
Blocking buffer: 3% nonfat dry milk in TBST.
Detection: ECL Basic Kit (RM00020).
Exposure time: 45s.

ABclonal:Immunohistochemistry - [KD Validated] SGPL1 Rabbit mAb (A26855)

Immunohistochemistry analysis of paraffin-embedded Human kidney tissue using [KD Validated] SGPL1 Rabbit mAb (A26855) at a dilution of 1:200 (40x lens). High pressure antigen retrieval performed with 0.01M Citrate Buffer (pH 6.0) prior to IHC staining.

ABclonal:Immunohistochemistry - [KD Validated] SGPL1 Rabbit mAb (A26855)

Immunohistochemistry analysis of paraffin-embedded Human liver cancer tissue using [KD Validated] SGPL1 Rabbit mAb (A26855) at a dilution of 1:200 (40x lens). High pressure antigen retrieval performed with 0.01M Citrate Buffer (pH 6.0) prior to IHC staining.

ABclonal:Immunohistochemistry - [KD Validated] SGPL1 Rabbit mAb (A26855)

Immunohistochemistry analysis of paraffin-embedded Mouse testis tissue using [KD Validated] SGPL1 Rabbit mAb (A26855) at a dilution of 1:200 (40x lens). High pressure antigen retrieval performed with 0.01M Citrate Buffer (pH 6.0) prior to IHC staining.

ABclonal:Immunohistochemistry - [KD Validated] SGPL1 Rabbit mAb (A26855)

Immunohistochemistry analysis of paraffin-embedded Rat testis tissue using [KD Validated] SGPL1 Rabbit mAb (A26855) at a dilution of 1:200 (40x lens). High pressure antigen retrieval performed with 0.01M Citrate Buffer (pH 6.0) prior to IHC staining.

ABclonal:Immunofluorescence - [KD Validated] SGPL1 Rabbit mAb (A26855)

Confocal imaging of paraffin-embedded Mouse small intesine tissue using [KD Validated] SGPL1 Rabbit mAb (A26855, dilution 1:200) followed by a further incubation with Cy3 Goat Anti-Rabbit IgG (H+L) (AS007, dilution 1:500) (Red). DAPI was used for nuclear staining (Blue). High pressure antigen retrieval performed with 0.01M Citrate Buffer(pH 6.0) prior to IF staining. Objective: 40x.

ABclonal:Immunofluorescence - [KD Validated] SGPL1 Rabbit mAb (A26855)

Confocal imaging of paraffin-embedded Rat thymus tissue using [KD Validated] SGPL1 Rabbit mAb (A26855, dilution 1:200) followed by a further incubation with Cy3 Goat Anti-Rabbit IgG (H+L) (AS007, dilution 1:500) (Red). DAPI was used for nuclear staining (Blue). High pressure antigen retrieval performed with 0.01M Citrate Buffer(pH 6.0) prior to IF staining. Objective: 40x.

ABclonal:Immunofluorescence - [KD Validated] SGPL1 Rabbit mAb (A26855)

Confocal imaging of Hep G2 cells using [KD Validated] SGPL1 Rabbit mAb (A26855, dilution 1:200) followed by a further incubation with Cy3 Goat Anti-Rabbit IgG (H+L) (AS007, dilution 1:500) (Red). The cells were counterstained with α-tubulin Mouse mAb (AC012, dilution 1:400) followed by incubation with ABflo® 488-conjugated Goat Anti-Mouse IgG (H+L) Ab (AS076, dilution 1:500) (Green). DAPI was used for nuclear staining (Blue). Objective: 100x.

ABclonal:Immunofluorescence - [KD Validated] SGPL1 Rabbit mAb (A26855)

Confocal imaging of 293T cells using [KD Validated] SGPL1 Rabbit mAb (A26855, dilution 1:200) followed by a further incubation with Cy3 Goat Anti-Rabbit IgG (H+L) (AS007, dilution 1:500) (Red). DAPI was used for nuclear staining (Blue). Objective: 100x.

Overview

Product name[KD Validated] SGPL1 Rabbit mAb
Catalog No.A26855
Host speciesRabbit
Purification methodAffinity purification
IsotypeIgG
CloneNo.ARC70997
Enables sphinganine-1-phosphate aldolase activity. Involved in apoptotic signaling pathway; fatty acid metabolic process; and sphingolipid metabolic process. Located in endoplasmic reticulum. Implicated in nephrotic syndrome type 14.
ImmunogenA synthetic peptide corresponding to a sequence within amino acids 301-400 of human SGPL1 (NP_003892.2).
SequenceVAKLAVKYKIPLHVDACLGGFLIVFMEKAGYPLEHPFDFRVKGVTSISADTHKYGYAPKGSSLVLYSDKKYRNYQFFVDTDWQGGIYASPTIAGSRPGGI
Gene ID
Swiss Prot
SynonymsSPL; S1PL; NPHS14
Calculated MW64kDa
Observed MW60kDa
ReactivityHuman, Mouse, Rat
Tested applicationsWBIHC-PIF/ICCIPChIPChIP-seqRIPFCFC(Intra)ELISAMeDIPNucleotide ArrayDBFACSCoIPCUT&TagmeRIPInhibition
Recommended dilution
  • WB 1:7500 - 1:30000
  • IHC-P 1:100 - 1:400
  • IF/ICC 1:200 - 1:800
  • ELISA Recommended starting concentration is 1 μg/mL. Please optimize the concentration based on your specific assay requirements.
Storage bufferStore at -20℃. Avoid freeze / thaw cycles.
Buffer: PBS with 0.09% Sodium azide, 0.05% BSA, 50% glycerol, pH7.3.
Key applicationWestern blotting    Immunohistochemistry    Immunofluorescence    
Positive samples293T, Hep G2, Rat thymus
Cellular locationEndoplasmic reticulum membrane, Single-pass type III membrane protein.

Documents

Certificate of Compliance

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ABclonal:Western blot - [KD Validated] SGPL1 Rabbit mAb (A26855)}

Western blot - [KD Validated] SGPL1 Rabbit mAb (A26855)

Western blot analysis of lysates from wild type (WT) and SGPL1 knockout (KD) 293T cells using [KD Validated] SGPL1 Rabbit mAb (A26855) at 1:15000 dilution incubated overnight at 4℃.
Secondary antibody: HRP-conjugated Goat anti-Rabbit IgG (H+L) (AS014) at 1:10000 dilution.
Lysates/proteins: 25 μg per lane.
Blocking buffer: 3% nonfat dry milk in TBST.
Detection: ECL Basic Kit (RM00020).
Exposure time: 45s.
ABclonal:Western blot - [KD Validated] SGPL1 Rabbit mAb (A26855)}

Western blot - [KD Validated] SGPL1 Rabbit mAb (A26855)

Western blot analysis of various lysates using [KD Validated] SGPL1 Rabbit mAb (A26855) at 1:15000 dilution incubated overnight at 4℃.
Secondary antibody: HRP-conjugated Goat anti-Rabbit IgG (H+L) (AS014) at 1:10000 dilution.
Lysates/proteins: 25 μg per lane.
Blocking buffer: 3% nonfat dry milk in TBST.
Detection: ECL Basic Kit (RM00020).
Exposure time: 45s.
ABclonal:Immunohistochemistry - [KD Validated] SGPL1 Rabbit mAb (A26855)}

Immunohistochemistry - [KD Validated] SGPL1 Rabbit mAb (A26855)

Immunohistochemistry analysis of paraffin-embedded Human kidney tissue using [KD Validated] SGPL1 Rabbit mAb (A26855) at a dilution of 1:200 (40x lens). High pressure antigen retrieval performed with 0.01M Citrate Buffer (pH 6.0) prior to IHC staining.
ABclonal:Immunohistochemistry - [KD Validated] SGPL1 Rabbit mAb (A26855)}

Immunohistochemistry - [KD Validated] SGPL1 Rabbit mAb (A26855)

Immunohistochemistry analysis of paraffin-embedded Human liver cancer tissue using [KD Validated] SGPL1 Rabbit mAb (A26855) at a dilution of 1:200 (40x lens). High pressure antigen retrieval performed with 0.01M Citrate Buffer (pH 6.0) prior to IHC staining.
ABclonal:Immunohistochemistry - [KD Validated] SGPL1 Rabbit mAb (A26855)}

Immunohistochemistry - [KD Validated] SGPL1 Rabbit mAb (A26855)

Immunohistochemistry analysis of paraffin-embedded Mouse testis tissue using [KD Validated] SGPL1 Rabbit mAb (A26855) at a dilution of 1:200 (40x lens). High pressure antigen retrieval performed with 0.01M Citrate Buffer (pH 6.0) prior to IHC staining.
ABclonal:Immunohistochemistry - [KD Validated] SGPL1 Rabbit mAb (A26855)}

Immunohistochemistry - [KD Validated] SGPL1 Rabbit mAb (A26855)

Immunohistochemistry analysis of paraffin-embedded Rat testis tissue using [KD Validated] SGPL1 Rabbit mAb (A26855) at a dilution of 1:200 (40x lens). High pressure antigen retrieval performed with 0.01M Citrate Buffer (pH 6.0) prior to IHC staining.
ABclonal:Immunofluorescence - [KD Validated] SGPL1 Rabbit mAb (A26855)}

Immunofluorescence - [KD Validated] SGPL1 Rabbit mAb (A26855)

Confocal imaging of paraffin-embedded Mouse small intesine tissue using [KD Validated] SGPL1 Rabbit mAb (A26855, dilution 1:200) followed by a further incubation with Cy3 Goat Anti-Rabbit IgG (H+L) (AS007, dilution 1:500) (Red). DAPI was used for nuclear staining (Blue). High pressure antigen retrieval performed with 0.01M Citrate Buffer(pH 6.0) prior to IF staining. Objective: 40x.
ABclonal:Immunofluorescence - [KD Validated] SGPL1 Rabbit mAb (A26855)}

Immunofluorescence - [KD Validated] SGPL1 Rabbit mAb (A26855)

Confocal imaging of paraffin-embedded Rat thymus tissue using [KD Validated] SGPL1 Rabbit mAb (A26855, dilution 1:200) followed by a further incubation with Cy3 Goat Anti-Rabbit IgG (H+L) (AS007, dilution 1:500) (Red). DAPI was used for nuclear staining (Blue). High pressure antigen retrieval performed with 0.01M Citrate Buffer(pH 6.0) prior to IF staining. Objective: 40x.
ABclonal:Immunofluorescence - [KD Validated] SGPL1 Rabbit mAb (A26855)}

Immunofluorescence - [KD Validated] SGPL1 Rabbit mAb (A26855)

Confocal imaging of Hep G2 cells using [KD Validated] SGPL1 Rabbit mAb (A26855, dilution 1:200) followed by a further incubation with Cy3 Goat Anti-Rabbit IgG (H+L) (AS007, dilution 1:500) (Red). The cells were counterstained with α-tubulin Mouse mAb (AC012, dilution 1:400) followed by incubation with ABflo® 488-conjugated Goat Anti-Mouse IgG (H+L) Ab (AS076, dilution 1:500) (Green). DAPI was used for nuclear staining (Blue). Objective: 100x.
ABclonal:Immunofluorescence - [KD Validated] SGPL1 Rabbit mAb (A26855)}

Immunofluorescence - [KD Validated] SGPL1 Rabbit mAb (A26855)

Confocal imaging of 293T cells using [KD Validated] SGPL1 Rabbit mAb (A26855, dilution 1:200) followed by a further incubation with Cy3 Goat Anti-Rabbit IgG (H+L) (AS007, dilution 1:500) (Red). DAPI was used for nuclear staining (Blue). Objective: 100x.

* For research use only. Not for therapeutic or diagnostic purposes.

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