REEP5 Polyclonal Antibody, Invitrogen™
Manufacturer: Thermo Scientific
Select a Size
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| Each of 1 | PIPA5106289-Each-of-1 | In Stock | ₹ 46,502.50 |
PIPA5106289 - Each of 1
In Stock
Quantity
1
Base Price: ₹ 46,502.50
GST (18%): ₹ 8,370.45
Total Price: ₹ 54,872.95
Antigen
REEP5
Classification
Polyclonal
Conjugate
Unconjugated
Gene
REEP5
Gene Alias
AI324241; AU022809; AW495741; C5orf18; D5S346; deleted in polyposis 1; Dp1; DP1/TB2; GP106; polyposis coli region hypothetical protein DP1; polyposis locus protein 1; Polyposis locus protein 1 homolog; Protein TB2; protein TB2 homolog; R74856; receptor accessory protein 5; receptor expression enhancing protein 5; receptor expression-enhancing protein 5; Reep5; TB2; TB2/DP1; Yip2e; YOP1
Host Species
Rabbit
Purification Method
Affinity chromatography
Regulatory Status
RUO
Gene ID (Entrez)
13476, 364838, 7905
Content And Storage
-20°C
Form
Liquid
Applications
Immunohistochemistry (Paraffin), Western Blot
Concentration
1 mg/mL
Formulation
PBS with 50% glycerol and 0.02% sodium azide; pH 7.4
Gene Accession No.
B2RZ37, Q00765, Q60870
Gene Symbols
REEP5
Immunogen
A synthesized peptide derived from human REEP5(Accession Q00765), corresponding to amino acid residues M1-L49.
Quantity
100 μL
Primary or Secondary
Primary
Target Species
Human, Mouse, Rat
Product Type
Antibody
Isotype
IgG
Related Products
Description
- Antibody detects endogenous levels of total REEP5
- REEP5 (receptor expression-enhancing protein 5), also known as C5orf18, DP1, TB2 or D5S346, is a 189 amino acid multi-pass membrane protein
- Thought to promote the functional cell surface expression of olfactory receptors, REEP5 belongs to the DP1 family and is encoded by a gene that maps to chromosome 5
- With 181 million base pairs encoding around 1,000 genes, chromosome 5 is about 6% of human genomic DNA
- Chromosome 5 is associated with Cockayne syndrome through the ERCC8 gene and familial adenomatous polyposis through the adenomatous polyposis coli (APC) tumor suppressor gene
- Treacher Collins syndrome is also chromosome 5 associated and is caused by insertions or deletions within the TCOF1 gene
- Deletion of the parm of chromosome 5 leads to cri du chat syndrome
- Deletion of 5q or chromosome 5 altogether is common in therapy-related acute myelogenous leukemias and myelodysplastic syndrome.