TCTN3-Polyclonal Antibodies

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TCTN3

Qty


Total
$220
Catalog #
A0684
Antibody Type
Polyclonal Antibody
Gene ID
26123
Swiss Prot
Q6NUS6
Size
Species
Rabbit
Isotype
IgG
Purity
Affinity purification
Additional Information
ReactivityHuman Mouse Rat
Tested applicationsWB IHC
Recommended DilutionWB 1:500 - 1:2000 IHC 1:50 - 1:200
Calculated MW66kDa
Observed MWRefer to Figures
ImmunogenRecombinant protein of human TCTN3
Storage BufferStore at -20℃. Avoid freeze / thaw cycles. Buffer: PBS with 0.02% sodium azide, 50% glycerol, pH7.3.
Concentrationb
SynonymTCTN3;C10orf61;DKFZp564D116;TECT3 ;Tectonic-3;
Images
  • A0684: image 1

    Western blot analysis of various cell lines using TCTN3 antibody.

  • A0684: image 2

    Immunohistochemistry of paraffin-embedded human liver cancer using TCTN3 antibody at dilution of 1:100 (40x lens).

Background

Tect3 (tectonic-3), also known as TCTN3, is a 607 amino acid single-pass type I membrane protein that belongs to the tectonic family and exists as four alternatively spliced isoforms. Tect3 interacts with MKS1 and may be involved in apoptosis regulation. The gene that encodes Tect3 contains approximately 31,560 bases and maps to human chromosome 10q24.1. Spanning nearly 135 million base pairs and encoding nearly 1,200 genes, chromosome 10 makes up approximately 4.5% of the human genome. Several protein-coding genes, including those that encode chemokines, cadherins, excision repair proteins, early growth response factors (Egrs) and fibroblast growth receptors (FGFRs), are located on chromosome 10. Defects in some of the genes that map to chromosome 10 are associated with Charcot-Marie Tooth disease, Jackson-Weiss syndrome, Usher syndrome, nonsyndromatic deafness, Wolman’s syndrome, Cowden syndrome, Cockayne syndrome, multiple endocrine neoplasia type 2 and porphyria. Tetrahydrobiopterin deficiency and a number of syndromes involving defective skull and facial bone fusion are also linked to chromosome 10.

Protocol

N/A

MSDS
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