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TGM5 rabbit pAb

CAT: 0855-ES12736-01Size: 50 µLDry Ice: NoHazardous: No
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CAT#:0855-ES12736-01Size:50 µL
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Background
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]
Description
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
O43548
Swiss Prot
O43548
Reactivity
Human; Mouse
Immunogen
Synthesized peptide derived from human TGM5 AA range: 448-498
Target
TGM5
Clonality
Polyclonal
Source
Rabbit
Applications
WB
Concentration
1 mg/ml
Dilution
WB 1:500-2000
Buffer
-20°C/1 year
Storage Conditions
-20°C/1 year
Fragment
IgG
Subcellular Location
Cytoplasm . Associated with intermediate filaments.
Gene ID (Human)
9333

UniProtKB · O43548

Protein-glutamine gamma-glutamyltransferase 5

TGM5_HUMAN · Homo sapiens

View on UniProt ↗
Primary accession
O43548
Review status
UniProtKB reviewed (Swiss-Prot)
Gene
TGM5
Protein existence
1: Evidence at protein level
Organism
Homo sapiens (Human)
Taxonomy ID
9606
Alternative names
—
EC number
2.3.2.13
Processing
—
Secondary accessions
O43549, Q0VF40, Q9UEZ4
Protein keywords

PTM

Acetylation

Molecular function

AcyltransferaseTransferase

Coding sequence diversity

Alternative splicing

Ligand

CalciumMetal-binding

Cellular component

Cytoplasm

Technical term

Direct protein sequencingProteomics identificationReference proteome

Disease

Disease variant

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