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SAB2103297 Sigma

Anti-ATP6V1C1, (N-terminal) antibody produced in rabbit

affinity isolated antibody

Synonym: Anti-ATP6C, Anti-ATP6D, Anti-FLJ20057, Anti-VATC, Anti-Vma5

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Properties

Related Categories ATH-AZ, Alphabetical Index, Antibodies, Primary Antibodies
species reactivity   guinea pig, rabbit, canine, human, horse, bovine, zebrafish, mouse, rat
application(s)   western blot: suitable
clone   polyclonal
concentration   0.5 mg - 1 mg/mL
antibody form   affinity isolated antibody
form   buffered aqueous solution
mol wt   mol wt 42 kDa
shipped in   wet ice
storage temp.   −20°C
Gene Information   human ... ATP6V1C1(528)
biological source   rabbit
conjugate   unconjugated
NCBI accession no.   NM_001695

Description

Immunogen

The immunogen for anti-ATP6V1C1 antibody: synthetic peptide derected towards the N terminal of human ATP6V1C1

General description

ATP6V1C1 (ATPase H+ transporting V1 subunit C1) is a subunit and regulator of V-ATPase (vacuolar ATPase).

Physical form

Purified antibody supplied in 1x PBS buffer with 0.09% (w/v) sodium azide and 2% sucrose.

Features and Benefits

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Biochem/physiol Actions

ATP6V1C1 (ATPase H+ transporting V1 subunit C1) is overexpressed in breast cancer, where it modulates the actin structure in a way that it promotes metastasis. This gene is up-regulated in oral squamous cell carcinoma (OSCC).

Sequence

Synthetic peptide located within the following region: ldafvegvvkkvaqymadvledskdkvqenllangvdlvtyitrfqwdma

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Safety & Documentation

Safety Information

RIDADR  NONH for all modes of transport
WGK Germany  3
Protocols & Articles

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Antibody Explorer | Buy Primary & Secondary Antibodies

Monoclonal and polyclonal primary antibodies are focused on cell biology, neurobiology and molecular biology. Secondary antibodies targeting multiple host’s IgG are conjugated to alkaline phosphatase...
Keywords: Amplification, Buffers, Cell biology, Enzyme-linked immunosorbent assay, Immunofluorescence, Immunohistochemistry, Immunoprecipitation, Molecular biology, Phosphorylations, Purification, Western blot

Peer-Reviewed Papers
15

References

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