Full Product Name
TGM5 Antibody
Product Synonym Names
Transglutaminase 5, protein-glutamine gamma-glutamyltransferase 5, TGase-5, TGase X, TGMX, TGX
Product Gene Name
anti-TGM5 antibody
[Similar Products]
Research Use Only
For Research Use Only. Not for use in diagnostic procedures.
Species Reactivity
Human, Mouse, Rat
Specificity
TGM5 antibody is predicted to not cross-react with other TGase protein family members. Multiple isoforms of TGM5 are known to exist.
Purity/Purification
Affinity chromatography purified via peptide column
Form/Format
Supplied in PBS containing 0.02% sodium azide.
Immunogen Description
Raised against a 19 amino acid peptide near the carboxy terminus of human TGM5.
Preparation and Storage
Can be stored at -20 degree C, stable for one year. As with all antibodies care should be taken to avoid repeated freeze thaw cycles. Antibodies should not be exposed to prolonged high temperatures.
Other Notes
Small volumes of anti-TGM5 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.
Related Product Information for
anti-TGM5 antibody
Transglutaminases (TGM) are a family of structurally and functionally related Ca2+-dependent enzymes (TGases) that stabilize protein assemblies through the formation of gamma-glutamyl-epsilon lysine crosslinks. TGases influence numerous
biological processes, including blood coagulation, cell differentiation, fertilization and apoptosis. TGM5 belongs to the transglutaminase superfamily and catalyzes the cross-linking of proteins between glutamine and lysine residues, often resulting in stabilization of protein assemblies. TGM5 is also expressed in the human hair follicle. Defects in TGM5 are associated with acral peeling skin syndrome.
Product Categories/Family for anti-TGM5 antibody
Total protein Ab
Applications Tested/Suitable for anti-TGM5 antibody
ELISA (EIA), Western Blot (WB)
Western Blot (WB) of anti-TGM5 antibody
Western blot analysis of TGM5 in rat heart tissue lysate with TGM5 antibody at (A) 1 and (B) 2 ug/mL.

NCBI/Uniprot data below describe general gene information for TGM5. It may not necessarily be applicable to this product.
NCBI Accession #
NP_963925
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NCBI GenBank Nucleotide #
NM_201631.3
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UniProt Secondary Accession #
O43549; Q0VF40; Q9UEZ4[Other Products]
UniProt Related Accession #
O43548[Other Products]
Molecular Weight
71,919 Da
NCBI Official Full Name
protein-glutamine gamma-glutamyltransferase 5 isoform 1
NCBI Official Synonym Full Names
transglutaminase 5
NCBI Official Symbol
TGM5??[Similar Products]
NCBI Official Synonym Symbols
TGX; PSS2; TGM6; TGMX; TGASE5; TGASEX
??[Similar Products]
NCBI Protein Information
protein-glutamine gamma-glutamyltransferase 5
UniProt Protein Name
Protein-glutamine gamma-glutamyltransferase 5
UniProt Synonym Protein Names
Transglutaminase X; TG(X); TGX; TGase X; Transglutaminase-5; TGase-5
Protein Family
Protein-glutamine gamma-glutamyltransferase
UniProt Gene Name
TGM5??[Similar Products]
UniProt Synonym Gene Names
TGMX; TG(X); TGX; TGase X; TGase-5??[Similar Products]
UniProt Entry Name
TGM5_HUMAN
NCBI Summary for TGM5
This gene encodes a member of the transglutaminase family. The encoded protein catalyzes formation of protein cross-links between glutamine and lysine residues, often resulting in stabilization of protein assemblies. This reaction is calcium dependent. Mutations in this gene have been associated with acral peeling skin syndrome. [provided by RefSeq, Oct 2009]
UniProt Comments for TGM5
TGM5: Catalyzes the cross-linking of proteins and the conjugation of polyamines to proteins. Contributes to the formation of the cornified cell envelope of keratinocytes. Defects in TGM5 are a cause of peeling skin syndrome type A (APSS). A non-inflammatory form of peeling skin syndrome, a genodermatosis characterized by the continuous shedding of the outer layers of the epidermis. In APSS patients, skin peeling is strictly limited to the dorsa of the hands and feet, and it is accompanied by accompanied by painless erythema and spontaneous non-scarring healing. Ultrastructural and histological analysis shows a level of blistering high in the epidermis at the stratum granulosum-stratum corneum junction. Belongs to the transglutaminase superfamily. Transglutaminase family. 2 isoforms of the human protein are produced by alternative splicing.
Protein type: Transferase; EC 2.3.2.13
Chromosomal Location of Human Ortholog: 15q15.2
Cellular Component: cytoplasm
Molecular Function: protein-glutamine gamma-glutamyltransferase activity; metal ion binding
Biological Process: epidermis development; protein modification process; peptide cross-linking
Disease: Peeling Skin Syndrome 2
Research Articles on TGM5
1. Data trebles the number of TMG5 mutations and provides further evidence that pCly113Cys is a founder mutation in the European population.
Precautions
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