This website uses cookies to ensure you get the best experience on our website.
- Table of Contents
, No Gclids
Kbtbd13 Antibodies
AND Kbtbd13 ELISA kits, Kbtbd13 Proteins
Many biological assays use antibodies to detect Kbtbd13, such as Western Blot (WB), ELISA, Flow Cytometry, Immunocytochemistry (IHC). These antibodies can be polyclonal or monoclonal, and react with Kbtbd13 in Human, Mouse, Rat, and many other animal samples. Boster Bio use mainly mouse and rabbit to develop Kbtbd13 antibodies...
Previous: Septin9
Next: Tnks2
Kbtbd13 Infographic by Boster Bio
All Kbtbd13 Products
Product
Figures
Specificity
Applications
Price
Kbtbd13 Overview
Facts about Kelch repeat and BTB domain-containing protein 13.
Kelch repeat and BTB domain-containing protein 13 (Kbtbd13)
Substrate-specific adapter of a BCR (BTB-CUL3-RBX1) E3 ubiquitin ligase complex. .
.
Gene Information
| Mouse | |
|---|---|
| Gene Name: | Kbtbd13 |
| Uniprot: | Q8C828 |
| Entrez: | 74492 |
Family
| Belongs to: |
|---|
| No superfamily |
Alternative Names
HCG1645727; Kelch Repeat And BTB (POZ) Domain Containing 13; Kelch Repeat And BTB Domain-Containing Protein 13; NEM6; Nemaline Myopathy Type 6
Molecular Weight
Mass (kDA):
49.769 kDA
Genomic Context
| Mouse | |
|---|---|
| Location: | 9|9 C |
| Sequence: | 9; |
Tissue Specificity
Expressed in skeletal muscle, heart and lung.
Diseases
- Myopathy
- Myopathies, Nemaline
- Neuromuscular Diseases
Pathways
- Pathogenesis
- Myofibril Assembly
- Conjugation
PTMs
For details, visit:
bosterbio.com/bosterbio-gene-info-cards/Kbtbd13
bosterbio.com/bosterbio-gene-info-cards/Kbtbd13
References
PMID: 21109227 by Sambuughin N., et al. Dominant mutations in KBTBD13, a member of the BTB/Kelch family, cause nemaline myopathy with cores.