Product Name
Visual system homeobox 2 (VSX2), ELISA Kit
Full Product Name
Human Visual system homeobox 2 (VSX2) ELISA Kit
Product Gene Name
VSX2 elisa kit
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Research Use Only
For Research Use Only. Not for use in diagnostic procedures.
Request for Current Manual Insert
Request Current Manual
Samples
Serum, plasma, Cell Culture Supernatants, body fluid and tissue homogenate
Detection Range
0.5-10ng/mL
Preparation and Storage
Store all reagents at 2-8 degree C.
Sample Preparation
We suggest pre-experimenting with neat (undiluted) samples, 1:2 or 1:4 dilutions. Please avoid diluting your samples more than 1:10 as it would exceed the dilution limit set for this kit. If the expected concentration of the target is beyond the detection range of the kit, please contact our technical support team
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 VSX2 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 VSX2 purchase
MBS7222265 is a ready-to-use microwell, strip plate ELISA (enzyme-linked immunosorbent assay) Kit for analyzing the presence of the Visual system homeobox 2 (VSX2) 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 VSX2. The ELISA analytical biochemical technique of the MBS7222265 kit is based on VSX2 antibody-VSX2 antigen interactions (immunosorbency) and an HRP colorimetric detection system to detect VSX2 antigen targets in samples. The ELISA Kit is designed to detect native, not recombinant, VSX2. 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(%).
Product Categories/Family for VSX2 elisa kit
Epigenetics and Nuclear Signaling
NCBI/Uniprot data below describe general gene information for VSX2. It may not necessarily be applicable to this product.
NCBI Accession #
NP_878314.1
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NCBI GenBank Nucleotide #
NM_182894.2
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UniProt Secondary Accession #
A1A4X6[Other Products]
UniProt Related Accession #
P58304[Other Products]
Molecular Weight
39,411 Da
NCBI Official Full Name
visual system homeobox 2
NCBI Official Synonym Full Names
visual system homeobox 2
NCBI Official Symbol
VSX2 [Similar Products]
NCBI Official Synonym Symbols
RET1; CHX10; HOX10; MCOP2; MCOPCB3
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NCBI Protein Information
visual system homeobox 2; homeobox protein CHX10; ceh-10 homeodomain-containing homolog; ceh-10 homeo domain containing homolog
UniProt Protein Name
Visual system homeobox 2
UniProt Synonym Protein Names
Ceh-10 homeodomain-containing homolog; Homeobox protein CHX10
Protein Family
Visual system homeobox
UniProt Gene Name
VSX2 [Similar Products]
UniProt Synonym Gene Names
CHX10; HOX10 [Similar Products]
UniProt Entry Name
VSX2_HUMAN
NCBI Summary for VSX2
This gene encodes a homeobox protein originally described as a retina-specific transcription factor. Mutations in this gene are associated with microphthalmia, cataracts and iris abnormalities. [provided by RefSeq, Oct 2009]
UniProt Comments for VSX2
CHX10: Plays a significant role in the specification and morphogenesis of the sensory retina. May also participate in the development of the cells of the inner nuclear layer, particularly bipolar cells. Defects in VSX2 are the cause of microphthalmia isolated type 2 (MCOP2); also known as isolated clinical anophthalmia. Microphthalmia is a clinically heterogeneous disorder of eye formation, ranging from small size of a single eye to complete bilateral absence of ocular tissues. Ocular abnormalities like opacities of the cornea and lens, scaring of the retina and choroid, cataractand other abnormalities like cataract may also be present. Defects in VSX2 are the cause of microphthalmia with cataracts and iris abnormalities (MCOPCTI). Defects in VSX2 are the cause of microphthalmia isolated with coloboma type 3 (MCOPCB3); also known as isolated colobomatous microphthalmia 3. Ocular colobomas are a set of malformations resulting from abnormal morphogenesis of the optic cup and stalk, and the fusion of the fetal fissure (optic fissure). Belongs to the paired homeobox family.
Protein type: DNA-binding
Chromosomal Location of Human Ortholog: 14q24.3
Cellular Component: cytoplasm; nucleus
Molecular Function: sequence-specific DNA binding
Biological Process: negative regulation of cell proliferation; cell fate commitment; transcription, DNA-dependent; visual perception; positive regulation of cell proliferation; response to stimulus; positive regulation of transcription from RNA polymerase II promoter; retinal bipolar neuron differentiation
Disease: Microphthalmia, Isolated 2; Microphthalmia, Isolated, With Coloboma 3
Research Articles on VSX2
1. Mutations in VSX2 represent an important cause of autosomal recessive microphthalmia in consanguineous pedigrees.
Precautions
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Disclaimer
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