Product Name
ATPase, H+ transporting, lysosomal V0 subunit a4 (ATP6V0A4), ELISA Kit
Popular Item
Full Product Name
Human V-type proton ATPase 116 kDa subunit a isoform 4, ATP6V0A4 ELISA Kit
Product Synonym Names
Human V-type proton ATPase 116 kDa subunit a isoform 4 (ATP6V0A4) ELISA kit; tcag7.346; A4; ATP6N1B; ATP6N2; MGC130016; MGC130017; RDRTA2; RTA1C; RTADR; STV1; VPH1; VPP2; ATPase; H+ transporting; lysosomal (vacuolar proton pump) non-catalytic accessory protein 1B; ATPase; H+; ATPase; H+ transporting; lysosomal V0 subunit a4
Product Gene Name
ATP6V0A4 elisa kit
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Research Use Only
For Research Use Only. Not for use in diagnostic procedures.
Sample Manual Insert
Download Sample PDF Manual View Sample PDF Manual
Request for Current Manual Insert
Request Current Manual
3D Structure
ModBase 3D Structure for Q9HBG4
Specificity
No significant cross-reactivity or interference between this analyte and analogues is observed.
Samples
Body fluids, tissue homogenates, secretions or feces samples
Assay Type
Quantitative Sandwich
Detection Range
0.625 ng/ml - 20 ng/ml
Intra-assay Precision
Intra-assay CV (%) is less than 15%
Inter-assay Precision
Inter-assay CV (%) is less than 15%. [CV(%) = SD/mean ×100].
Preparation and Storage
Store all reagents at 2-8 degree C
Product Note
Select online data sheet information is drawn from bioinformatics databases, occasionally resulting in ambiguous or non-relevant product information. It is the responsibility of the customer to review, verify, and evaluate the information to make sure it matches their requirements before purchasing the kit. Our ELISA Kit assays are dynamic research tools and sometimes they may be updated and improved. If the format of this assay is important to you then please request the current manual or contact our technical support team with a presales inquiry before placing an order. We will confirm the current details of the assay. We cannot guarantee the sample manual posted online is the most current manual.
Other Notes
Small volumes of ATP6V0A4 elisa kit 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.
Searchable Terms for ATP6V0A4 purchase
MBS9327390 is a ready-to-use microwell, strip plate ELISA (enzyme-linked immunosorbent assay) Kit for analyzing the presence of the ATPase, H+ transporting, lysosomal V0 subunit a4 (ATP6V0A4) ELISA Kit target analytes in
biological samples. The concentration gradients of the kit standards or positive controls render a theoretical kit detection range in biological research samples containing ATP6V0A4. The ELISA analytical biochemical technique of the MBS9327390 kit is based on ATP6V0A4 antibody-ATP6V0A4 antigen interactions (immunosorbency) and an HRP colorimetric detection system to detect ATP6V0A4 antigen targets in samples. The ELISA Kit is designed to detect native, not recombinant, ATP6V0A4. Appropriate sample types may include undiluted body fluids and/or tissue homogenates, secretions. Quality control assays assessing reproducibility identified the intra-assay CV (%) and inter-assay CV(%).
Related Product Information for
ATP6V0A4 elisa kit
Background/Introduction: This Quantitative Sandwich ELISA kit is only for in vitro research use only, not for drug, household, therapeutic or diagnostic applications! This kit is intended to be used for determination the level of ATP6V0A4 (hereafter termed "analyte") in undiluted original Human body fluids, tissue homogenates, secretions or feces samples. This kit is NOT suitable for assaying non-biological sources of substances.
NCBI/Uniprot data below describe general gene information for ATP6V0A4. It may not necessarily be applicable to this product.
NCBI Accession #
NP_065683.2
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NCBI GenBank Nucleotide #
NM_020632.2
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UniProt Primary Accession #
Q9HBG4
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UniProt Secondary Accession #
Q32M47; A4D1R4; A8KA80[Other Products]
UniProt Related Accession #
Q9HBG4[Other Products]
Molecular Weight
96,386 Da
NCBI Official Full Name
V-type proton ATPase 116 kDa subunit a isoform 4
NCBI Official Synonym Full Names
ATPase, H+ transporting, lysosomal V0 subunit a4
NCBI Official Symbol
ATP6V0A4 [Similar Products]
NCBI Official Synonym Symbols
A4; STV1; VPH1; VPP2; RTA1C; RTADR; ATP6N2; RDRTA2; ATP6N1B
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NCBI Protein Information
V-type proton ATPase 116 kDa subunit a isoform 4; V-ATPase 116 kDa; vacuolar proton pump, subunit 2; vacuolar proton pump 116 kDa accessory subunit; vacuolar proton translocating ATPase 116 kDa subunit a kidney isoform; H(+)-transporting two-sector ATPase, noncatalytic accessory protein 1B; ATPase, H+ transporting, lysosomal (vacuolar proton pump) non-catalytic accessory protein 1B; ATPase, H+ transporting, lysosomal (vacuolar proton pump) non-catalytic accessory protein 2 (38kD)
UniProt Protein Name
V-type proton ATPase 116 kDa subunit a isoform 4
UniProt Synonym Protein Names
Vacuolar proton translocating ATPase 116 kDa subunit a isoform 4; Vacuolar proton translocating ATPase 116 kDa subunit a kidney isoform
Protein Family
V-type proton ATPase
UniProt Gene Name
ATP6V0A4 [Similar Products]
UniProt Synonym Gene Names
ATP6N1B; ATP6N2; V-ATPase 116 kDa isoform a4 [Similar Products]
UniProt Entry Name
VPP4_HUMAN
NCBI Summary for ATP6V0A4
This gene encodes a component of vacuolar ATPase (V-ATPase), a multisubunit enzyme that mediates acidification of intracellular compartments of eukaryotic cells. V-ATPase dependent 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. This gene is one of four genes in man and mouse that encode different isoforms of the a subunit. Alternatively spliced transcript variants encoding the same protein have been described. Mutations in this gene are associated with renal tubular acidosis associated with preserved hearing. [provided by RefSeq, Jul 2008]
UniProt Comments for ATP6V0A4
ATP6V0A4: Part of the proton channel of the V-ATPase that is involved in normal vectorial acid transport into the urine by the kidney. Defects in ATP6V0A4 are the cause of distal renal tubular acidosis with preserved hearing (RTADR). RTADR is an autosomal recessive form of distal renal tubular acidosis (dRTA), a group of disorders characterized by functional failure of alpha- intercalated cells of the cortical collecting duct of the distal nephron, where vectorial proton transport is required for urinary acidification. Functional failure of alpha-intercalated cells results in metabolic acidosis accompanied by disturbances of potassium balance, urinary calcium solubility, bone physiology and growth. Belongs to the V-ATPase 116 kDa subunit family.
Protein type: Transporter, ion channel; Membrane protein, integral; Transporter; Energy Metabolism - oxidative phosphorylation; Membrane protein, multi-pass; Transporter, iron
Chromosomal Location of Human Ortholog: 7q34
Cellular Component: phagocytic vesicle membrane; brush border membrane; apical part of cell; lysosomal membrane; apical plasma membrane; integral to membrane; plasma membrane; endosome membrane; vacuolar proton-transporting V-type ATPase complex; endosome
Molecular Function: protein binding; hydrogen ion transporting ATPase activity, rotational mechanism; ATPase binding
Biological Process: vacuolar acidification; interaction with host; ATP synthesis coupled proton transport; ossification; proton transport; sensory perception of sound; cellular iron ion homeostasis; ATP hydrolysis coupled proton transport; insulin receptor signaling pathway; transferrin transport; regulation of pH; excretion; transmembrane transport
Disease: Renal Tubular Acidosis, Distal, Autosomal Recessive
Research Articles on ATP6V0A4
1. Mutations of the ATP6V0A4 gene is associated with primary distal renal tubular acidosis.
Precautions
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Disclaimer
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