Product Name
Hyccin (HCC), ELISA Kit
Full Product Name
Human Hyccin (HCC) ELISA Kit
Product Gene Name
HCC elisa kit
[Similar Products]
Research Use Only
For Research Use Only. Not for use in diagnostic procedures.
Request for Current Manual Insert
Request Current Manual
Chromosome Location
Chromosome: 7; NC_000007.13 (22980878..23053770, complement). Location: 7p15.3
3D Structure
ModBase 3D Structure for Q9BYI3
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 HCC 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 HCC purchase
MBS9311956 is a ready-to-use microwell, strip plate ELISA (enzyme-linked immunosorbent assay) Kit for analyzing the presence of the Hyccin (HCC) 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 HCC. The ELISA analytical biochemical technique of the MBS9311956 kit is based on HCC antibody-HCC antigen interactions (immunosorbency) and an HRP colorimetric detection system to detect HCC antigen targets in samples. The ELISA Kit is designed to detect native, not recombinant, HCC. 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(%).
NCBI/Uniprot data below describe general gene information for HCC. It may not necessarily be applicable to this product.
NCBI Accession #
NP_115970.2
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NCBI GenBank Nucleotide #
NM_032581.3
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UniProt Primary Accession #
Q9BYI3
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UniProt Secondary Accession #
Q6N010; Q75MR4; Q7LDZ4; Q96MX1; Q96NQ6; A4D145[Other Products]
UniProt Related Accession #
Q9BYI3[Other Products]
Molecular Weight
57,625 Da
NCBI Official Full Name
hyccin
NCBI Official Synonym Full Names
family with sequence similarity 126, member A
NCBI Official Symbol
FAM126A [Similar Products]
NCBI Official Synonym Symbols
HCC; HLD5; HYCC1; DRCTNNB1A
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NCBI Protein Information
hyccin; down regulated by Ctnnb1, a; down-regulated by CTNNB1 protein A
UniProt Protein Name
Hyccin
UniProt Synonym Protein Names
Down-regulated by CTNNB1 protein A; Protein FAM126A
Protein Family
Hemocyanin
UniProt Gene Name
FAM126A [Similar Products]
UniProt Synonym Gene Names
DRCTNNB1A [Similar Products]
UniProt Entry Name
HYCCI_HUMAN
NCBI Summary for HCC
The protein encoded by this gene may play a part in the beta-catenin/Lef signaling pathway. Expression of this gene is down-regulated by beta-catenin. Defects in this gene are a cause of hypomyelination with congenital cataract (HCC). [provided by RefSeq, Oct 2008]
UniProt Comments for HCC
FAM126A: May have a role in the beta-catenin/Lef signaling pathway. May have a role in the process of myelination of the central and peripheral nervous system. Defects in FAM126A are the cause of leukodystrophy hypomyelinating type 5 (HLD5). This disorder is characterized by congenital cataract, progressive neurologic impairment, and diffuse myelin deficiency. Affected individuals experience progressive pyramidal and cerebellar dysfunction, muscle weakness and wasting prevailingly in the lower limbs. Mental deficiency ranges from mild to moderate. Belongs to the FAM126 family. 2 isoforms of the human protein are produced by alternative splicing.
Protein type: Motility/polarity/chemotaxis
Chromosomal Location of Human Ortholog: 7p15.3
Cellular Component: cytoplasm; plasma membrane
Molecular Function: signal transducer activity
Biological Process: signal transduction
Disease: Leukodystrophy, Hypomyelinating, 5
Research Articles on HCC
1. Two novel mutations in the FAM126A gene were identified in 2 unrelated families with Hypomyelination and congenital cataract
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.