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A1486

Sigma-Aldrich

Anti-ATP6AP1 (451-465) antibody produced in rabbit

IgG fraction of antiserum, PBS solution

Sinônimo(s):

Anti-16A, Anti-ATP6IP1, Anti-ATP6S1, Anti-Ac45, Anti-CF2, Anti-VATPS1, Anti-Vacuolar ATP synthase subunit S1 precursor, Anti-XAP3

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About This Item

Código UNSPSC:
12352203
NACRES:
NA.41

fonte biológica

rabbit

Nível de qualidade

200

conjugado

unconjugated

forma do anticorpo

IgG fraction of antiserum

tipo de produto de anticorpo

primary antibodies

clone

polyclonal

Formulário

PBS solution

peso molecular

antigen ~52 kDa

reatividade de espécies

human

técnica(s)

western blot: 1:500-1:2,000

nº de adesão UniProt

Q15904

Condições de expedição

dry ice

temperatura de armazenamento

−20°C

modificação pós-traducional do alvo

unmodified

Informações sobre genes

human ... ATP6AP1(537)

Descrição geral

ATPase H+ transporting accessory protein 1 (ATP6AP1) is an accessory subunit of the V-ATPase. This gene is located on human chromosome Xq28. ATP6AP1 is also referred as Ac45. It is abundantly expressed a high levels in neuronal and (neuro-) endocrine cells and osteoclasts.

Imunogênio

synthetic peptide corresponding to amino acids 451-465 of human ATP6AP1

Aplicação

Rabbit anti-ATP6AP1 (451-465) antibody can be used for western blot (1:500-1:2,000) assays.
Yale Center for High Throughput Cell Biology IF-tested antibodies. Each antibody is tested by immunofluorescence against HUVEC cells using the Yale HTCB IF protocol. To learn more about us and Yale Center for High Throughput Cell Biology partnership, visit sigma.com/htcb-if.

Ações bioquímicas/fisiológicas

ATPase H+ transporting accessory protein 1 (ATP6AP1) is known to cause an X-linked N-glycosylation syndrome with liver disease. It is essential for endosomal acidification. It also participates in membrane trafficking and Ca2+-dependent membrane fusion.

forma física

Solution in 0.01 M phosphate buffered saline, pH 7.4, containing 15 mM sodium azide.

Exoneração de responsabilidade

Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.

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Código de classe de armazenamento

12 - Non Combustible Liquids

Classe de risco de água (WGK)

nwg

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Certificados de análise (COA)

Lot/Batch Number
069K2827

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Expanding the phenotype of metabolic cutis laxa with an additional disorder of N-linked protein glycosylation
Witters P, et al.
European Journal of Human Genetics, 26(5), 618-618 (2018)
Loss-of-function mutations in ATP6AP1 and ATP6AP2 in granular cell tumors
Pareja F, et al.
Nature Communications, 9(1), 3533-3533 (2018)
Richard J Nuckels et al.
Investigative ophthalmology & visual science, 50(2), 893-905 (2008-10-07)
The vacuolar (v)-ATPase complex is a key regulator of the acidification of endosomes, lysosomes, and the luminal compartments of several cell types, tissues, and organs; however, little is know about the in vivo function of the v-ATPase complex or its
Jason J Gokey et al.
Developmental biology, 407(1), 115-130 (2015-08-09)
Asymmetric fluid flows generated by motile cilia in a transient 'organ of asymmetry' are involved in establishing the left-right (LR) body axis during embryonic development. The vacuolar-type H(+)-ATPase (V-ATPase) proton pump has been identified as an early factor in the
Fresia Pareja et al.
Nature communications, 9(1), 3533-3533 (2018-09-01)
Granular cell tumors (GCTs) are rare tumors that can arise in multiple anatomical locations, and are characterized by abundant intracytoplasmic granules. The genetic drivers of GCTs are currently unknown. Here, we apply whole-exome sequencing and targeted sequencing analysis to reveal
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