EML1 Polyclonal Antibody, Invitrogen™
Manufacturer: Thermo Scientific
Select a Size
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| Each of 1 | PIPA530016-Each-of-1 | In Stock | ₹ 46,502.50 |
PIPA530016 - Each of 1
In Stock
Quantity
1
Base Price: ₹ 46,502.50
GST (18%): ₹ 8,370.45
Total Price: ₹ 54,872.95
Antigen
EML1
Classification
Polyclonal
Conjugate
Unconjugated
Gene
EML1
Gene Alias
1110008N23Rik; A930030P13Rik; AA171013; AI847476; AI853955; echinoderm microtubule associated protein like 1; echinoderm microtubule associated protein-like protein 1; echinoderm microtubule-associated protein-like 1; ELP79; EMAP; EMAP1; EMAP-1; EMAPL; EMAPL1; Eml1; HuEMAP; huEMAP-1
Host Species
Rabbit
Purification Method
Antigen affinity chromatography
Regulatory Status
RUO
Gene ID (Entrez)
2009, 68519
Content And Storage
Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.
Form
Liquid
Applications
Western Blot
Concentration
0.62 mg/mL
Formulation
0.1M tris glycine with 20% glycerol and 0.01% thimerosal; pH 7
Gene Accession No.
O00423, Q05BC3
Gene Symbols
EML1
Immunogen
Recombinant fragment corresponding to a region within amino acids 32 and 349 of Human EML1
Quantity
100 μL
Primary or Secondary
Primary
Target Species
Human, Mouse
Product Type
Antibody
Isotype
IgG
Related Products
Description
- Recommended positive controls: A549, HeLa, HepG2, mouse brain
- Predicted reactivity: Mouse (93%), Rat (93%)
- Store product as a concentrated solution
- Centrifuge briefly prior to opening the vial
- Human echinoderm microtubule-associated protein-like is a strong candidate for the Usher syndrome type 1A gene
- Usher syndromes (USHs) are a group of genetic disorders consisting of congenital deafness, retinitis pigmentosa, and vestibular dysfunction of variable onset and severity depending on the genetic type
- The disease process in USHs involves the entire brain and is not limited to the posterior fossa or auditory and visual systems
- The USHs are categorized as type I (USH1A, USH1B, USH1C, USH1D, USH1E and USH1F), type II (USH2A and USH2B) and type III (USH3)
- The type I is the most severe form
- Gene loci responsible for these three types are all mapped
- Two transcript variants encoding different isoforms have been found for this gene.