PA550771
SNX29 Polyclonal Antibody, Invitrogen™
Manufacturer: Thermo Scientific
Select a Size
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| Each of 1 | PA550771-Each-of-1 | In Stock | ₹ 46,502.50 |
PA550771 - Each of 1
In Stock
Quantity
1
Base Price: ₹ 46,502.50
GST (18%): ₹ 8,370.45
Total Price: ₹ 54,872.95
Antigen
SNX29
Classification
Polyclonal
Conjugate
Unconjugated
Gene
SNX29
Gene Alias
4933437K13Rik; A-388D4.1; ENSMUSG00000079738; Gm11170; Gm1737; Gm930; RUN domain containing 2A; RUN domain-containing protein 2A; RUNDC2A; SNX29; SODD; sorting nexin 29; sorting nexin-29
Host Species
Rabbit
Purification Method
Antigen affinity chromatography
Regulatory Status
RUO
Gene ID (Entrez)
92017
Content And Storage
-20°C
Form
Liquid
Applications
Immunohistochemistry (Paraffin)
Concentration
1.1 mg/mL
Formulation
PBS with 40% glycerol and 0.05% sodium azide; pH 7.4
Gene Accession No.
Q8TEQ0
Gene Symbols
SNX29
Immunogen
Synthetic peptide corresponding to residues near the C terminal of human sorting nexin 29
Quantity
100 μL
Primary or Secondary
Primary
Target Species
Human
Product Type
Antibody
Isotype
IgG
Related Products
Description
- The antibody detects endogenous levels of total RUNDC2A protein
- SNX29 also known as RUNDC2A, is a 375 amino protein that contains one RUN domain
- RUNDC2A is encoded by a gene that maps to human chromosome 16p13.13, which encodes over 900 genes and comprises nearly 3% of the human genome
- The GAN gene is located on chromosome 16 and, with mutation, may lead to giant axonal neuropathy, a nervous system disorder characterized by increasing malfunction with growth
- The rare disorder Rubinstein-Taybi syndrome is also associated with chromosome 16, as is Crohn's disease, which is a gastrointestinal inflammatory condition.