Goat Polyclonal V5 tag antibody. Suitable for ICC, ELISA, WB, IHC-P and reacts with Tag samples. Cited in 13 publications.
pH: 7.2
Preservative: 0.1% Sodium azide
Constituents: PBS
ICC | ELISA | WB | IHC-P | |
---|---|---|---|---|
Tag | Expected | Expected | Tested | Tested |
Species | Dilution info | Notes |
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Species Tag | Dilution info Use at an assay dependent concentration. | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Tag | Dilution info - | Notes Coating: 2 - 10 ug/ml; Primary: 0.03 - 1 ug/ml |
Species | Dilution info | Notes |
---|---|---|
Species Tag | Dilution info - | Notes Colorimetric: 0.1 - 1 ug/ml; Chemiluminescent: 0.03 - 1 ug/ml |
Species | Dilution info | Notes |
---|---|---|
Species Tag | Dilution info - | Notes - |
Select an associated product type
GKPIPNPLLGLDST epitope tag, GKPIPNPLLGLDST tag, Protein Rev, Regulator of expression of viral proteins, V5 epitope tag
Goat Polyclonal V5 tag antibody. Suitable for ICC, ELISA, WB, IHC-P and reacts with Tag samples. Cited in 13 publications.
pH: 7.2
Preservative: 0.1% Sodium azide
Constituents: PBS
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The V5 tag is an epitope tag derived from the P and V fusion proteins of the paramyxovirus. It typically measures around 14 amino acids in length and is often used in molecular biology for tagging and protein expression studies. In terms of mechanical function the V5 tag facilitates the detection characterization and purification of recombinant proteins. Scientists commonly use it in various hosts such as bacteria yeast and mammalian cells due to its convenient integration into larger protein complexes. Unlike native proteins it serves as a non-disruptive label for identifying proteins without affecting their functionality.
Researchers employ the V5 tag to decipher protein localization expression and role within cellular environments. It allows easy tracking in situ by using antibodies that target the V5 epitope such as the anti-V5 antibody. The V5 tag proves effective in dual-tagging systems useful in elucidating protein interactions and complex formations for instance when combined with other tags like biotin tag or APC tag. This assists in isolating and identifying components of complex cellular machinery.
The tag is frequently utilized in studies exploring functional pathways of various proteins across metabolic and signaling pathways. It aids in examining the relationship between proteins within signaling cascades by tagging proteins that interact with others such as those in the PK tag-related signaling pathways. Researchers often track proteins across intricate networks to understand cellular processes intricately using V5-tagged proteins as indicators or reporters.
Scientists harness the V5 tag to investigate the expression and interactions of proteins associated with certain conditions such as cancer and neurodegenerative diseases. Through its integration scientists aim to uncover alterations in protein interactions or localizations that contribute to disease progression. For example they may tag proteins linked to cancer pathways observing how disruptions in proteins related to anti-V5 targets could provide insights into tumor biology or pathogenesis.
We have tested this species and application combination and it works. It is covered by our product promise.
We have not tested this specific species and application combination in-house, but expect it will work. It is covered by our product promise.
This species and application combination has not been tested, but we predict it will work based on strong homology. However, this combination is not covered by our product promise.
We do not recommend this combination. It is not covered by our product promise.
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Full details and terms and conditions can be found here:
Terms & Conditions.
A, cells expressing 315-HARE, 190-HARE, or EV alone were cultured in T-25 flasks until confluent, washed, scraped, and lysed. Cell lysates (100ug of protein) were immunoprecipitated (IP) with anti-Tyr(P) mAb and the immune complexes were subjected to 5% SDS-PAGE and Western blot (WB) analysis using anti-V5 pAb. Cells expressing 315-HARE (B) or 190-HARE (C) cDNA were grown until confluent, washed, incubated for 1 h in medium without serum, and then incubated with (HA) or without (Ctr) 5ug/ml HA for 20 min. The cells were lysed and 200 ug of total lysate protein was immunoprecipitated with anti-HARE mAb-30. Immune complexes were collected and subjected to 5% SDS-PAGE and Western analysis using anti- Tyr(P) mAb. The same blots in B and C were reprobed with anti-V5 Ab (D and E, respectively). Immunopurification using non-immune mouse IgG served as another control in B–E. The solid and open arrows indicate the positions of the 315-HARE and 190-HARE, respectively.
All lanes: Western blot - Anti-V5 tag antibody (ab95038)
All lanes: Western blot - Anti-V5 tag antibody (ab95038) at 0.4 µg/mL
Lane 1: E. coli whole cell lysate expressing a multi-tag fusion protein at 0.2 µg
Lane 2: E. coli whole cell lysate expressing a multi-tag fusion protein at 0.1 µg
Lane 3: E. coli whole cell lysate expressing a multi-tag fusion protein at 0.05 µg
Developed using the ECL technique.
Exposure time: 30s
Immunohistochemical analysis of murine mammary tumour tissue, expressing vector (left) or V5-tagged Cadm1 (right), staining V5 tag with ab95038.
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