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ATP6V1B1, Antibody

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产品名称: ATP6V1B1, Antibody
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简单介绍

ATP6V1B1, Antibody


ATP6V1B1, Antibody  的详细介绍
Product Name

ATP6V1B1, Antibody

Full Product Name

ATP6V1B1 Antibody

Product Synonym Names
Vacuolar ATP synthase subunit B; kidney isoform; V-ATPase subunit B 1; Vacuolar proton pump subunit B 1; Endomembrane proton pump 58 kDa subunit; ATP6V1B1; ATP6B1; VATB; VPP3
Product Gene Name

anti-ATP6V1B1 antibody

[Similar Products]
Research Use Only
For Research Use Only. Not for use in diagnostic procedures.
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OMIM
192132
3D Structure
ModBase 3D Structure for P15313
Species Reactivity
Human, Mouse
Specificity
ATP6V1B1 Antibody detects endogenous levels of total ATP6V1B1
Purity/Purification
Immunogen affinity purified
Form/Format
In phosphate buffered saline, pH 7.4, 150mM NaCl, 0.02% sodium azide and 50% glycerol.
Immunogen
A synthesized peptide
Preparation and Storage
Store at-20 degree C for 1 year
Other Notes
Small volumes of anti-ATP6V1B1 antibody vial(s) may occasionally become entrapped in the seal of the product vial during shipment and storage. If necessary, briefly centrifuge the vial on a tabletop centrifuge to dislodge any liquid in the container`s cap. Certain products may require to ship with dry ice and additional dry ice fee may apply.
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Applications Tested/Suitable for anti-ATP6V1B1 antibody
Western Blot (WB), Immunohistochemistry (IHC)
Application Notes for anti-ATP6V1B1 antibody
WB: 1:500~1:1000
IHC: 1:50~1:200

Western Blot (WB) of anti-ATP6V1B1 antibody
Western blot analysis of extracts from HepG2 cells, using ATP6V1B1 antibody.
anti-ATP6V1B1 antibody Western Blot (WB) (WB) image
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NCBI/Uniprot data below describe general gene information for ATP6V1B1. It may not necessarily be applicable to this product.
NCBI GI #
19913426
NCBI GeneID
525
NCBI Accession #
NP_001683.2 [Other Products]
NCBI GenBank Nucleotide #
NM_001692.3 [Other Products]
UniProt Primary Accession #
P15313 [Other Products]
UniProt Secondary Accession #
Q53FY0; Q6P4H6[Other Products]
UniProt Related Accession #
P15313[Other Products]
Molecular Weight
60 KD
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NCBI Official Full Name
V-type proton ATPase subunit B, kidney isoform
NCBI Official Synonym Full Names
ATPase H+ transporting V1 subunit B1
NCBI Official Symbol
ATP6V1B1  [Similar Products]
NCBI Official Synonym Symbols
VATB; VMA2; VPP3; RTA1B; ATP6B1
  [Similar Products]
NCBI Protein Information
V-type proton ATPase subunit B, kidney isoform
UniProt Protein Name
V-type proton ATPase subunit B, kidney isoform
UniProt Synonym Protein Names
Endomembrane proton pump 58 kDa subunit; Vacuolar proton pump subunit B 1
Protein Family
V-type proton ATPase
UniProt Gene Name
ATP6V1B1  [Similar Products]
UniProt Synonym Gene Names
ATP6B1; VATB; VPP3; V-ATPase subunit B 1  [Similar Products]
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NCBI Summary for ATP6V1B1
This gene encodes 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. The V1 domain consists of three A and three B subunits, two G subunits plus the C, D, E, F, and H subunits. The V1 domain contains the ATP catalytic site. The V0 domain consists of five different subunits: a, c, c', c'', and d. Additional isoforms of many of the V1 and V0 subunit proteins are encoded by multiple genes or alternatively spliced transcript variants. This encoded protein is one of two V1 domain B subunit isoforms and is found in the kidney. Mutations in this gene cause distal renal tubular acidosis associated with sensorineural deafness. [provided by RefSeq, Jul 2008]
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UniProt Comments for ATP6V1B1
Non-catalytic subunit of the peripheral V1 complex of vacuolar ATPase. V-ATPase is responsible for acidifying a variety of intracellular compartments in eukaryotic cells.
Research Articles on ATP6V1B1
1. A novel c.1169dupC frameshift mutation of ATP6V1B1 gene was identified in one family and the c.1155dupC North African mutation in 2 other families. Both mutations are located in exon 12 of ATP6V1B1 gene in Moroccan patients with recessive form of distal renal tubular acidosis associated with precocious hearing loss.
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Precautions
All of MyBioSource's Products are for scientific laboratory research purposes and are not for diagnostic, therapeutics, prophylactic or in vivo use. Through your purchase, you expressly represent and warrant to MyBioSource that you will properly test and use any Products purchased from MyBioSource in accordance with industry standards. MyBioSource and its authorized distributors reserve the right to refuse to process any order where we reasonably believe that the intended use will fall outside of our acceptable guidelines.
Disclaimer
While every efforts were made to ensure the accuracy of the information provided in this datasheet, MyBioSource will not be liable for any omissions or errors contained herein. MyBioSource reserves the right to make changes to this datasheet at any time without prior notice.

It is the responsibility of the customer to report product performance issues to MyBioSource within 30 days of receipt of the product. Please visit our Terms & Conditions page for more information.
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