HRP Anti-SNX27 antibody [1C6] (ab203648)
![HRP Anti-SNX27 antibody [1C6] (ab203648)](https://www.abcam.com/ps/products/203/ab203648/Images/ab203648-248503-WBab2036481.jpg "HRP Anti-SNX27 antibody [1C6] (ab203648)")
Key features and details
- HRP Mouse monoclonal [1C6] to SNX27
- Suitable for: WB
- Reacts with: Human
- Conjugation: HRP
- Isotype: IgG1
Overview
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Product name
HRP Anti-SNX27 antibody [1C6]
See all SNX27 primary antibodies -
Description
HRP Mouse monoclonal [1C6] to SNX27 -
Host species
Mouse -
Conjugation
HRP -
Tested Applications & Species
See all applications and species dataApplication Species WB Human
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Immunogen
Fusion protein within Human SNX27 (N terminal). The exact sequence is proprietary.
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Epitope
N-terminal amino acids 1-267. -
Positive control
- WB: HeLa, HEK293 and MDA-MB-231 whole cell lysates.
Properties
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Form
Liquid -
Storage instructions
Shipped at 4°C. Store at +4°C short term (1-2 weeks). Upon delivery aliquot. Store at -20°C. Avoid freeze / thaw cycle. Store In the Dark. -
Storage buffer
pH: 7.40
Preservative: 0.1% 10% Proclin 300 Solution
Constituents: PBS, 30% Glycerol (glycerin, glycerine), 1% BSA -
Concentration information loading... -
Purity
Affinity purified -
Clonality
Monoclonal -
Clone number
1C6 -
Myeloma
Sp2/0 -
Isotype
IgG1 -
Research areas
Images
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Western blot - HRP Anti-SNX27 antibody [1C6] (ab203648)All lanes : HRP Anti-SNX27 antibody [1C6] (ab203648) at 1/5000 dilution
Lane 1 : HeLa (Human epithelial carcinoma cell line) Whole Cell Lysate
Lane 2 : HEK293 (Human embryonic kidney cell line) Whole Cell Lysate
Lane 3 : MDA-MB-361 (Human breast adenocarcinoma cell line) Whole Cell Lysate Whole Cell Lysate
Lysates/proteins at 10 µg per lane.
Developed using the ECL technique.
Performed under reducing conditions.
Predicted band size: 61 kDa
Observed band size: 61 kDa
Exposure time: 1 minuteThis blot was produced using a 4-12% Bis-tris gel under the MOPS buffer system. The gel was run at 200V for 50 minutes before being transferred onto a Nitrocellulose membrane at 30V for 70 minutes. The membrane was then blocked for an hour using 2% Bovine Serum Albumin before being incubated with ab203648 overnight at 4°C. Antibody binding was visualised using ECL development solution ab133406.
