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Anti-ATP6V1F Antibody (aa82-111) LS-C159141

Catalog Size Price
LS-C159141-400 400 µl Unavailable

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17 ATP6V1F Antibodies

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Anti-ATP6V1F Antibody (clone 5F10) IHC-plus™ LS-B11773
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Anti-ATP6V1F Antibody (clone 1B8) LS-C337230
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Anti-ATP6V1F Antibody LS-C659719
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100% Guaranteed
Rabbit Polyclonal to Human ATP6V1F
Western blot


Human ATP6V1F
Human (tested or 100% immunogen sequence identity)
Cow (at least 90% immunogen sequence identity)
Protein A purified


Western blot (1:1000)

Specificity and Use

LS-E6416 - Lyophilized - 100 µg - $145.00
Immunizing peptide used to generate LS-C159141. Useful for pre-absorption and neutralization of the antibody's antigen binding site.
This ATP6V1F antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 82-111 amino acids from the C-terminal region of human ATP6V1F.


PBS, 0.09% sodium azide
Maintain refrigerated at 2-8°C for up to 6 months. For long term storage store at -20°C.
For research use only.

About ATP6V1F

Q16864 NM_004231 NP_004222.2

ATP6V1F Antibody, ATPase, vacuolar, 14 kD Antibody, V-ATPase subunit F Antibody, Vacuolar proton pump F subunit Antibody, Vma7 Antibody, V-ATPase F subunit Antibody, ATP6S14 Antibody, Vacuolar proton pump subunit F Antibody, V-ATPase 14 kDa subunit Antibody, V-type proton ATPase subunit F Antibody, VATF Antibody

ATP6V1F is a component of vacuolar ATPase (V-ATPase), a multisubunit enzyme that mediates acidification of eukaryotic intracellular organelles. V-ATPase dependent organelle acidification is necessary for such intracellular processes as protein sorting, zymogen activation, receptor-mediated endocytosis, and synaptic vesicle proton gradient generation. V-ATPase is composed of a cytosolic V1 domain and a transmembrane V0 domain.

Western blot

ATP6V1F Antibody western blot of Jurkat cell line lysates (35 ug/lane). The ATP6V1F antibody detected the ATP6V1F protein (arrow).
ATP6V1F Antibody western blot of Jurkat cell line lysates (35 ug/lane). The ATP6V1F antibody detected the ATP6V1F protein (arrow).

Requested From: 
Date Requested: 4/21/2018

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