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遺伝子ノックアウト細胞株 検証済

Anti-Syntenin 抗体 (ab19903)

  • Datasheet
Reviews (4)Q&A (3)References (24)

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Abpromise

保証された製品品質、優れたカスタマー・サポート。 詳細はこちら。

Western blot - Anti-Syntenin antibody (ab19903)
  • Western blot - Anti-Syntenin antibody (ab19903)
  • Western blot - Anti-Syntenin antibody (ab19903)
  • Immunocytochemistry/ Immunofluorescence - Anti-Syntenin antibody (ab19903)

Key features and details

  • Rabbit polyclonal to Syntenin
  • Suitable for: ICC/IF, WB
  • Knockout validated
  • Reacts with: Mouse, Rat, Human
  • Isotype: IgG

リコンビナント抗体で、ロット間での高い再現性を実現

Product image
Anti-Syntenin antibody [EPR8102] (ab133267)
  • 異なるロット間での安定した再現性
  • 容易なスケールアップ
  • 評価試験による特異性の確認済み
  • 倫理基準に準拠 - アニマル・フリーの生産

製品の概要

  • 製品名

    Anti-Syntenin antibody
    Syntenin 一次抗体 製品一覧
  • 製品の詳細

    Rabbit polyclonal to Syntenin
  • 由来種

    Rabbit
  • アプリケーション

    適用あり: ICC/IF, WBmore details
  • 種交差性

    交差種: Mouse, Rat, Human
    交差が予測される動物種: Xenopus laevis, Monkey, Zebrafish
  • 免疫原

    Synthetic peptide. This information is proprietary to Abcam and/or its suppliers.

  • 特記事項

    The Life Science industry has been in the grips of a reproducibility crisis for a number of years. Abcam is leading the way in addressing this with our range of recombinant monoclonal antibodies and knockout edited cell lines for gold-standard validation. Please check that this product meets your needs before purchasing.

    If you have any questions, special requirements or concerns, please send us an inquiry and/or contact our Support team ahead of purchase. Recommended alternatives for this product can be found below, along with publications, customer reviews and Q&As

製品の特性

  • 製品の状態

    Liquid
  • 保存方法

    Shipped at 4°C. Store at +4°C short term (1-2 weeks). Upon delivery aliquot. Store at -20°C or -80°C. Avoid freeze / thaw cycle.
  • バッファー

    pH: 7.40
    Preservative: 0.02% Sodium azide
    Constituent: PBS

    Batches of this product that have a concentration < 1mg/ml may have BSA added as a stabilising agent. If you would like information about the formulation of a specific lot, please contact our scientific support team who will be happy to help.
  • Concentration information loading...
  • 精製度

    Immunogen affinity purified
  • ポリ/モノ

    ポリクローナル
  • アイソタイプ

    IgG
  • 研究分野

    • Neuroscience
    • Cell Type Marker
    • Neuron marker
    • Synapse marker
    • Neuroscience
    • Neurology process
    • Neurogenesis

関連製品

  • Compatible Secondaries

    • Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) (ab150077)
    • Goat Anti-Rabbit IgG H&L (HRP) (ab205718)
  • Isotype control

    • Rabbit IgG, polyclonal - Isotype Control (ChIP Grade) (ab171870)
  • Recombinant Protein

    • Recombinant Human Syntenin protein (ab185832)

アプリケーション

The Abpromise guarantee

Abpromise保証は、 次のテスト済みアプリケーションにおけるab19903の使用に適用されます

アプリケーションノートには、推奨の開始希釈率がありますが、適切な希釈率につきましてはご検討ください。

アプリケーション Abreviews 特記事項
ICC/IF (1)
Use a concentration of 1 µg/ml.
WB (1)
Use a concentration of 1 µg/ml. Detects a band of approximately 32 kDa (predicted molecular weight: 32 kDa).
特記事項
ICC/IF
Use a concentration of 1 µg/ml.
WB
Use a concentration of 1 µg/ml. Detects a band of approximately 32 kDa (predicted molecular weight: 32 kDa).

ターゲット情報

  • 機能

    Seems to function as an adapter protein. In adherens junctions may function to couple syndecans to cytoskeletal proteins or signaling components. Seems to couple transcription factor SOX4 to the IL-5 receptor (IL5RA). May also play a role in vesicular trafficking. Seems to be required for the targeting of TGFA to the cell surface in the early secretory pathway.
  • 組織特異性

    Widely expressed. Expressed in fetal kidney, liver, lung and brain. In adult highest expression in heart and placenta.
  • 配列類似性

    Contains 2 PDZ (DHR) domains.
  • 翻訳後修飾

    Phosphorylated on tyrosine residues.
  • 細胞内局在

    Cell junction > focal adhesion. Cell junction > adherens junction. Cell membrane. Endoplasmic reticulum membrane. Nucleus. Melanosome. Cytoplasm > cytosol. Cytoplasm > cytoskeleton. Mainly membrane-associated. Localized to adherens junctions, focal adhesions and endoplasmic reticulum. Colocalized with actin stress fibers. Also found in the nucleus. Identified by mass spectrometry in melanosome fractions from stage I to stage IV.
  • Target information above from: UniProt accession O00560 The UniProt Consortium
    The Universal Protein Resource (UniProt) in 2010
    Nucleic Acids Res. 38:D142-D148 (2010) .

    Information by UniProt
  • 参照データベース

    • Entrez Gene: 6386 Human
    • Entrez Gene: 53378 Mouse
    • Entrez Gene: 83841 Rat
    • Entrez Gene: 447442 Xenopus laevis
    • Entrez Gene: 325004 Zebrafish
    • Omim: 602217 Human
    • SwissProt: O00560 Human
    • SwissProt: O08992 Mouse
    • SwissProt: Q9JI92 Rat
    • Unigene: 200804 Human
    • Unigene: 247473 Mouse
    • Unigene: 483278 Mouse
    • Unigene: 4309 Rat
    see all
  • 別名

    • MDA-9 antibody
    • MDA9 antibody
    • Melanoma differentiation-associated protein 9 antibody
    • Pro-TGF-alpha cytoplasmic domain-interacting protein 18 antibody
    • Scaffold protein Pbp1 antibody
    • SDCB1_HUMAN antibody
    • SDCBP antibody
    • ST1 antibody
    • SYCL antibody
    • Syndecan binding protein (syntenin) antibody
    • Syndecan binding protein 1 antibody
    • Syndecan-binding protein 1 antibody
    • Syntenin 1 antibody
    • Syntenin-1 antibody
    • TACIP18 antibody
    see all

画像

  • Western blot - Anti-Syntenin antibody (ab19903)
    Western blot - Anti-Syntenin antibody (ab19903)

    Lane 1: Wild-type HAP1 whole cell lysate (20 µg)
    Lane 2: Syntenin knockout HAP1 whole cell lysate (20 µg)
    Lane 3: A549 whole cell lysate (20 µg)
    Lane 4: HeLa whole cell lysate (20 µg)

    Lanes 1-4: Merged signal (red and green). Green - ab19903 observed at 32 kDa. Red - loading control, ab130007, observed at 130 kDa.

    ab19903 was shown to recognize Syntenin in wild-type HAP1 cells as signal was lost at the expected MW in Syntenin knockout cells. Additional cross-reactive bands were observed in the wild-type and knockout cells. Wild-type and Syntenin knockout samples were subjected to SDS-PAGE. ab19903 and ab130007 (Mouse anti-Vinculin loading control) were incubated overnight at 4°C at 1 μg/ml and 1/20000 dilution respectively. Blots were developed with Goat anti-Rabbit IgG H&L (IRDye® 800CW) preabsorbed ab216773 and Goat anti-Mouse IgG H&L (IRDye® 680RD) preabsorbed ab216776 secondary antibodies at 1/20000 dilution for 1 hour at room temperature before imaging.

  • Western blot - Anti-Syntenin antibody (ab19903)
    Western blot - Anti-Syntenin antibody (ab19903)
  • Western blot - Anti-Syntenin antibody (ab19903)
    Western blot - Anti-Syntenin antibody (ab19903)
    All lanes : Anti-Syntenin antibody (ab19903) at 1 µg/ml

    Lane 1 : Mouse heart lysate
    Lane 2 : Rat heart lysate
    Lane 3 : Mouse heart lysate with Mouse Syntenin peptide (ab20431) at 1 µg/ml
    Lane 4 : Rat heart lysate with Mouse Syntenin peptide (ab20431) at 1 µg/ml

    Lysates/proteins at 20 µg per lane.

    Secondary
    All lanes : Goat Anti-Rabbit IgG H&L (HRP) (ab6721) at 1/50000 dilution

    Predicted band size: 32 kDa
    Observed band size: 32 kDa
    Additional bands at: 50 kDa. We are unsure as to the identity of these extra bands.



    ab19903 detects a band of the expected size (32kDa) in both mouse and rat heart lysate. This band is quenched completely by the addition of the immunizing peptide in the mouse lysate and is partially quenched by the addition of ab20431 in the rat heart lysate.
  • Immunocytochemistry/ Immunofluorescence - Anti-Syntenin antibody (ab19903)
    Immunocytochemistry/ Immunofluorescence - Anti-Syntenin antibody (ab19903)
    ICC/IF image of ab19903 stained human HEK 293 cells. The cells were PFA fixed (10 min), permabilised in TBS-T (20 min) and incubated with the antibody (ab19903, 1µg/ml) for 1h at room temperature. 1%BSA / 10% normal goat serum / 0.3M glycine was used to quench autofluorescence and block non-specific protein-protein interactions. The secondary antibody (green) was Alexa Fluor® 488 goat anti-rabbit IgG (H+L) used at a 1/1000 dilution for 1h. Alexa Fluor® 594 WGA was used to label plasma membranes (red). DAPI was used to stain the cell nuclei (blue).

プロトコール

  • Immunohistochemistry protocols
  • Immunocytochemistry & immunofluorescence protocols
  • Western blot protocols

Click here to view the general protocols

データシートおよび資料

  • Datasheet download

    Download

参考文献 (24)

ab19903 を使用した論文を発表された方は、こちらまでお知らせください。データシートに掲載させていただきます。

ab19903 は 24 報の論文で使用されています。

  • Zhang Y  et al. Phosphatase Shp2 regulates biogenesis of small extracellular vesicles by dephosphorylating Syntenin. J Extracell Vesicles 10:e12078 (2021). PubMed: 33732417
  • Balbi C  et al. Circulating extracellular vesicles are endowed with enhanced procoagulant activity in SARS-CoV-2 infection. EBioMedicine 67:103369 (2021). PubMed: 33971404
  • Larios J  et al. ALIX- and ESCRT-III-dependent sorting of tetraspanins to exosomes. J Cell Biol 219:N/A (2020). PubMed: 32049272
  • Nakamura Y  et al. Adiponectin Stimulates Exosome Release to Enhance Mesenchymal Stem-Cell-Driven Therapy of Heart Failure in Mice. Mol Ther 28:2203-2219 (2020). PubMed: 32652045
  • Matthies D  et al. Microdomains form on the luminal face of neuronal extracellular vesicle membranes. Sci Rep 10:11953 (2020). PubMed: 32686698
View all Publications for this product

レビューと Q&A

Show All レビュー Q&A
レビューを送る 質問を送る

1-7 of 7 Abreviews or Q&A

Immunocytochemistry abreview for Anti-Syntenin antibody

Excellent
Abreviews
Abreviews
abreview image
Application
Immunocytochemistry
Sample
Rat Cultured Cells (Hippocampus)
Permeabilization
Yes - PBS with Triton 0.25%
Specification
Hippocampus
Blocking step
BSA as blocking agent for 30 minute(s) · Concentration: 3% · Temperature: 20°C
Fixative
Paraformaldehyde
Read More

Luis Martins

Verified customer

投稿 May 31 2017

Immunohistochemistry (PFA perfusion fixed frozen sections) abreview for Anti-Syntenin antibody

Excellent
Abreviews
Abreviews
abreview image
Application
Immunohistochemistry (PFA perfusion fixed frozen sections)
Sample
Mouse Tissue sections (Brain)
Specification
Brain
Read More

DR. Sophie Pezet

Verified customer

投稿 May 04 2011

Immunocytochemistry/ Immunofluorescence abreview for Anti-Syntenin antibody

Average
Abreviews
Abreviews
abreview image
Application
Immunocytochemistry/ Immunofluorescence
Sample
Xenopus laevis Cell (meiotic egg extract)
Specification
meiotic egg extract
Fixative
pre-fixation in formaldehyde and Methanol fixation after extract spindown onto coverslips
Permeabilization
No
Blocking step
BSA as blocking agent for 1 hour(s) and 0 minute(s) · Concentration: 3% · Temperature: 25°C
Read More

Abcam user community

Verified customer

投稿 Mar 03 2010

Western blot abreview for Anti-Syntenin antibody

Good
Abreviews
Abreviews
abreview image
Application
Western blot
Sample
Xenopus laevis Cell lysate - other (meiotic egg extract)
Loading amount
25 µg
Specification
meiotic egg extract
Gel Running Conditions
Reduced Denaturing (10%)
Blocking step
Milk as blocking agent for 1 hour(s) and 0 minute(s) · Concentration: 5% · Temperature: 25°C
Read More

Abcam user community

Verified customer

投稿 Mar 03 2010

Question

Dear
Thanks for your kindly reply, after contact this customer, she would like to have a credit note, could you please help her to create a credit note ?
I deeply appreciate your great assistance!

Read More

Abcam community

Verified customer

Asked on May 01 2012

Answer

Thank you for you reply.

Your credit note ID is XXXXX.

If payment has already been made on the original order and you wish to receive a refund, please ask your purchasing department to contact our accounting department so that we may gather the correct information needed for the refund. To avoid confusion, please ensure your accounts department is aware of how the credit note is being used.

Please refer to the credit note ID in any correspondence with our accounting department.

The credit note ID is for your reference only and does not automatically guarantee the credit.

I hope this experience will not prevent you from purchasing other products from us in the future. Our Scientific Support team is always at your service, should you require further expert advice.

Read More

Abcam Scientific Support

Answered on May 01 2012

Question

Dear technical support team:
This customer has purchased ab19903 (Anti-Syntenin antibody) and has conducted the IHC assay with human sample sever times. The results show weak signal, therefore, she wants to ask for your help to modify her experiment step, could you please offer any suggestion to help her?
I also attached her data in this letter and her experiment step as follow:
1) Order details:

˙Batch number (Lot number): XXXXXXX
Po: XXXXXX
˙Abcam product code: ab19903
˙Antibody storage conditions (temperature/reconstitution etc) : -20
2) Please describe the problem (high background, non-specific signal…etc).
Weak signal
3) On what material are you testing the antibody in IHC/ICC?

˙Species: human

˙What’s cell line or tissue: lung cancer tissue

4) Sample preparation:

˙Type of sample (Fresh frozen sections, perfusion fixed frozen sections, PFA/formalin fixed

˙paraffin embedded sections, cells in culture, other:____) : paraffin embedded sections

˙Sample preparation:

˙Positive control: Hearttissue

˙Negative control:

5) Fixation step

˙Yes or No : Yes

˙If yes, Fixative agent and concentration: 10% Formalin

˙Fixation time: 2 days

˙Fixation temperature : RT

6) Antigen retrieval method(including time, temperature etc.):

Antigen Retrieval AR-10 solution (BioGenex) 121℃ 10min ( autoclave )

7) Permeabilization method:

˙Did you do a permeabilization step (details please) or add permeabilizing agent in any dilution buffers?

˙Permeabilizing agent and concentration:

8) Blocking agent (eg BSA, serum…):

˙Concentration: BioGenex Power Block

˙Blocking time : 20min

˙Blocking temperature: RT

9)

˙Endogenous peroxidases blocked? 3% H2O2, 10min

˙Endogenous biotins blocked? No

10) Primary antibody (If more than one was used, describe in “additional notes”) :

˙Species: Rabbit

˙Reacts against: Mouse, Rat, Human, Xenopus laevis

˙At what dilution(s) have you tested this antibody: 1:20

˙Diluent buffer: Antibody Diluent buffer (Ventana)

˙Incubation time: 2hr

˙Incubation temperature: RT

˙What washing steps were done (which buffer, number of washes): PBST

11) Secondary antibody:

˙Species: Super Sensitive Non-Biotin Polymer HRP Detection System BioGenex

˙Reacts against which species:

˙At what dilution(s) have you tested this antibody:

˙Diluent buffer:

˙Incubation time:

˙What washing steps were done (which buffer, number of washes):

˙Fluorochrome or enzyme conjugate (eg: FITC, HRP, AP, biotin…etc):

˙Do you know whether the problems you are experiencing come from the secondary?

12) Signal amplification method (eg: ABC, LSAB, HRP polymer, TSE): HRP polymer

13) Detection method (eg: DAB, BCIP/NBT …etc): DAB

14)

˙ How many times have you run this staining? 2 times

˙Do you obtain the same results every time? Yes

˙What steps have you altered to try and optimize the use of this antibody?

Could you please help this customer to solve the problem?

Thanks for your kindly help

Best regards

Read More

Abcam community

Verified customer

Asked on Apr 17 2012

Answer

I am sorry to hear you have been experiencing problems with one of our antibodies. The quality of our products is important to us and I would like to reassure you that we investigate all customer complaints. I appreciate the time taken to submit protocol information as well as an image to us and I would like to make some suggestions to the protocol in an attempt to improve the results obtained.

-In order to check whether the antibody is working properly, I would encourage you to use it in a tissue with high levels of the protein. According to the Human Protein Atlas, this protein is highly expressed in brain, so it could serve as a good indicator of the antibodies performance.

http://www.proteinatlas.org/ENSG00000137575

-The optimal fixation process occurs between 12 to 24 hours. If the tissue is over fixed it may well be the antibody is unable to reach the epitope.

-We usually recommend optimisation of the Antigen Retrieval method, in order to adapt it to the specific antibodies and samples used. A control experiment is recommended beforehand, where slides of the same tissue section are retrieved for 5, 10, 15, 20, 25 and 30 minutes before being immunohistochemically stained to evaluate optimum antigen retrieval time for the particular antibody being used. In the following link you will find useful information for the different antigen retrieval methods:

https://www.abcam.com/index.html?pageconfig=resource&rid=11488#notes2

It is also useful trying different buffers. In our lab we tend to use tris EDTA as it often gives successful results.

-I am not aware of the blocking agent used, but in any case, this step may also be optimised if weak staining is observed. Try milder conditions (e.g., blocking for less time, decreasing the temperature, or different agents) in an attempt to improve the results.

-We also recommend incubating the primary antibody over night at 4C to get a better staining.

-Please make sure the primary antibody and the detection system used are compatible and work successfully in other assays.

In any case, all of our products are covered by our Abpromise guarantee which ensures that you can trust our products, and they should work in the tested species and applications stated on the datasheet, or we will offer a replacement, credit, or refund, if reported within 6 months of purchase.

I hope this information is helpful. Should the suggestions not improve the results, please do not hesitate to contact me again and I will try to provide further help.

Read More

Abcam Scientific Support

Answered on Apr 17 2012

Question

ab19903: mouse heart tissue lysate and membrane fraction no bands block: 2% milk or BSA Ab: 1/500, 1/2000 secondary: tried two different, work fine 100 uf protein loaded

Read More

Abcam community

Verified customer

Asked on Dec 22 2011

Answer

Thank you for your phone call. As we discussed I am issuing you a credit note (for refund) for ab19903. Your credit note ID is xxx. I am sorry that this antibody did not perform as stated on the datasheet. If payment has already been made on the original order and you wish to receive a refund, please ask your purchasing department to contact our accounting department so that we may gather the correct information needed for the refund. To avoid confusion, please ensure your accounts department is aware of how the credit note is being used. Our accounting department can be contacted by email at us.credits@abcam.com or by telephone using the information at the Contact Us link in the top right corner of our website. Please refer to the credit note ID in any correspondence with our accounting department. The credit note ID is for your reference only and does not automatically guarantee the credit. I hope this experience will not prevent you from purchasing other products from us in the future. Our Scientific Support team is always at your service, should you require further expert advice. If you have any further questions, please just let me know.

Read More

Abcam Scientific Support

Answered on Dec 22 2011

Please note: All products are "FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC PROCEDURES"
For licensing inquiries, please contact partnerships@abcam.com

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