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Filaggrin, Polyclonal Antibody

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产品名称: Filaggrin, Polyclonal Antibody
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简单介绍

Filaggrin, Polyclonal Antibody


Filaggrin, Polyclonal Antibody  的详细介绍
Product Name

Filaggrin (FLG), Polyclonal Antibody

Full Product Name

Rabbit anti-human Filaggrin polyclonal Antibody, FITC

Product Gene Name

anti-FLG antibody

[Similar Products]
Research Use Only
For Research Use Only. Not for use in diagnostic procedures.
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OMIM
135940
3D Structure
ModBase 3D Structure for P20930
Clonality
Polyclonal
Isotype
IgG
Host
Rabbit
Species Reactivity
Human
Purity/Purification
Caprylic Acid Ammonium Sulfate Precipitation Purified
Storage Buffer
Preservative: 0.03% Proclin 300
Constituents: 50% Glycerol, 0.01M PBS, PH 7.4
Conjugate
FITC
Immunogen
Recombinant human Filaggrin protein
Santa Cruz Alternative
Potential replacement for Santa Cruz Biotechnology antibody catalog# sc-25896 / sc-25897 / sc-30229
Preparation and Storage
Shipped at 4 degree C. Upon delivery aliquot and store at -20 degree C or -80 degree C. Avoid repeated freeze.
ISO Certification
Manufactured in an ISO 13485:2003 and EN ISO 13485:2012 Certified Laboratory.
Other Notes
Small volumes of anti-FLG 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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Related Product Information for
anti-FLG antibody
Aggregates keratin intermediate filaments and promotes disulfide-bond formation among the intermediate filaments during terminal differentiation of mammalian epidermis.
Applications Tested/Suitable for anti-FLG antibody
ELISA (EIA)
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NCBI/Uniprot data below describe general gene information for FLG. It may not necessarily be applicable to this product.
NCBI GI #
60097902
NCBI GeneID
2312
NCBI Accession #
NP_002007.1 [Other Products]
NCBI GenBank Nucleotide #
NM_002016.1 [Other Products]
UniProt Primary Accession #
P20930 [Other Products]
UniProt Secondary Accession #
Q01720; Q5T583; Q9UC71[Other Products]
UniProt Related Accession #
P20930[Other Products]
Molecular Weight
435,170 Da
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NCBI Official Full Name
filaggrin
NCBI Official Synonym Full Names
filaggrin
NCBI Official Symbol
FLG  [Similar Products]
NCBI Official Synonym Symbols
ATOD2
  [Similar Products]
NCBI Protein Information
filaggrin
UniProt Protein Name
Filaggrin
Protein Family
Filaggrin
UniProt Gene Name
FLG  [Similar Products]
UniProt Entry Name
FILA_HUMAN
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NCBI Summary for FLG
The protein encoded by this gene is an intermediate filament-associated protein that aggregates keratin intermediate filaments in mammalian epidermis. It is initially synthesized as a polyprotein precursor, profilaggrin (consisting of multiple filaggrin units of 324 aa each), which is localized in keratohyalin granules, and is subsequently proteolytically processed into individual functional filaggrin molecules. Mutations in this gene are associated with ichthyosis vulgaris.[provided by RefSeq, Dec 2009]
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UniProt Comments for FLG
FLG: Aggregates keratin intermediate filaments and promotes disulfide-bond formation among the intermediate filaments during terminal differentiation of mammalian epidermis. Defects in FLG are the cause of ichthyosis vulgaris (VI); also known as ichthyosis simplex. Ichthyosis vulgaris is the most common form of ichthyosis inherited as an autosomal dominant trait. It is characterized by palmar hyperlinearity, keratosis pilaris and a fine scale that is most prominent over the lower abdomen, arms, and legs. Ichthyosis vulgaris is characterized histologically by absent or reduced keratohyalin granules in the epidermis and mild hyperkeratosis. The disease can be associated with frequent asthma, eczema or hay fever. Defects in FLG are a cause of susceptibility to dermatitis atopic type 2 (ATOD2). Atopic dermatitis is a complex, inflammatory disease with multiple alleles at several loci thought to be involved in the pathogenesis. It commonly begins in infancy or early childhood and is characterized by a chronic relapsing form of skin inflammation, a disturbance of epidermal barrier function that culminates in dry skin, and IgE- mediated sensitization to food and environmental allergens. It is manifested by lichenification, excoriation, and crusting, mainly on the flexural surfaces of the elbow and knee. Belongs to the S100-fused protein family.

Protein type: Cytoskeletal

Chromosomal Location of Human Ortholog: 1q21.3

Cellular Component: intermediate filament; intracellular membrane-bound organelle; nucleus

Molecular Function: calcium ion binding; protein binding; structural molecule activity

Biological Process: keratinocyte differentiation; multicellular organismal development

Disease: Dermatitis, Atopic, 2; Ichthyosis Vulgaris
Research Articles on FLG
1. These results indicate that FLG mutations might be involved in the pathogenesis of wheat-dependent exercise-induced anaphylaxis in the family studied.
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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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