Vamp7

Manufactured by Novus Biologicals

VAMP7 is a protein that functions as a soluble N-ethylmaleimide-sensitive factor attachment protein receptor (SNARE) involved in intracellular membrane fusion and trafficking processes. It is a member of the vesicle-associated membrane protein (VAMP) family.

Automatically generated - may contain errors

Lab products found in correlation

Snap23, by Abcam (1 mentions) Rab27b, by Proteintech (1 mentions) Hrp conjugated anti mouse igg, by Cell Signaling Technology (1 mentions) Hrp conjugated anti rabbit igg, by Cell Signaling Technology (1 mentions) β actin, by Proteintech (1 mentions) Rab7 d95f2, by Cell Signaling Technology (1 mentions) Phalloidin ifluor 594 reagent, by Abcam (1 mentions) Gm130, by BD (1 mentions) Rab11, by BD (1 mentions)

Spelling variants of this product

Anti-VAMP7 (NB100-91356 (3 citations)

2 protocols using vamp7

Immunoblotting and Immunofluorescence Analysis of Extracellular Vesicle Proteins

Check if the same lab product or an alternative is used in the 5 most similar protocols

The antibodies used for immunoblotting and immunofluorescence were as follows: Cortactin (H222) (3503; Cell Signaling Technology), VAMP7 (NB100–91356; Novus Biologicals), RAB7 (D95F2) (9367 T; Cell Signaling Technology), RAB27B (13412–1-AP; Proteintech), CD63 (GTX28219; GeneTex), β-actin (20536–1-AP; Proteintech), TSG101(28283–1-AP; Proteintech), CD81(A5270; ABclonal), SNAP23 (ab4114; Abcam), HRP-conjugated anti-rabbit IgG (7074S; Cell Signaling Technology), and HRP-conjugated anti-mouse IgG (7076S; Cell Signaling Technology). The reagent used for immunoblotting was Phalloidin-iFluor 594 reagent (ab176757; Abcam).

Peng X., Li X., Yang S., Huang M., Wei S., Ma Y., Li Y., Wu B., Jin H., Li B., Tang S., Fan Q., Liu J., Yang L, & Li H. (2021). LINC00511 drives invasive behavior in hepatocellular carcinoma by regulating exosome secretion and invadopodia formation. Journal of Experimental & Clinical Cancer Research : CR, 40, 183.

+ Open protocol

+ Expand

Immunohistochemical Analysis of Kidney Cellular Markers

Check if the same lab product or an alternative is used in the 5 most similar protocols

Cells were washed with PBS, fixed with 4% paraformaldehyde, permeabilized with PBS-0.2% Triton X 100, and blocked with 5% FBS. Immunostaining were performed using the following primary antibodies: Cleaved Caspase 3 (CST #9664 1:500), Fluorescein labeled LTL (Vector #FL-1321 1:500), AQP2 (Santa Cruz #sc-9882 1:200), Fluorescein labeled DBA (Vector #FL-1031-5 1:500), Fluorescein labeled PNA (Vector # FL-1071-5 1:500), DPEP1 (Invitrogen #PA5-52984 1:200), CHMP1A (Proteintech #15761-1-AP 1:200), EEA1 (BD#610456 1:200), RAB5 (CST #3547 1:200), RAB7 (Sigma #R8779 1:200), RAB11 (BD #610658 1:200), VAMP7 (NOVUS #NBP1-07118 1:200), and GM130 (BD #610822 1:200).

Guan Y., Liang X., Ma Z., Hu H., Liu H., Miao Z., Linkermann A., Hellwege J.N., Voight B.F, & Susztak K. (2021). A single genetic locus controls both expression of DPEP1/CHMP1A and kidney disease development via ferroptosis. Nature Communications, 12, 5078.

+ Open protocol

+ Expand

About PubCompare

Our mission is to provide scientists with the largest repository of trustworthy protocols and intelligent analytical tools, thereby offering them extensive information to design robust protocols aimed at minimizing the risk of failures.

We believe that the most crucial aspect is to grant scientists access to a wide range of reliable sources and new useful tools that surpass human capabilities.

However, we trust in allowing scientists to determine how to construct their own protocols based on this information, as they are the experts in their field.

Ready to get started?

Revolutionizing how scientists
search and build protocols!