AMMECR1 Polyclonal Antibody, Invitrogen™
Manufacturer: Thermo Scientific
Select a Size
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| Each of 1 | PIPA530555-Each-of-1 | In Stock | ₹ 47,392.50 |
PIPA530555 - Each of 1
In Stock
Quantity
1
Base Price: ₹ 47,392.50
GST (18%): ₹ 8,530.65
Total Price: ₹ 55,923.15
Antigen
AMMECR1
Classification
Polyclonal
Conjugate
Unconjugated
Gene
AMMECR1
Gene Alias
6230420G18Rik; Alport syndrome mental retardation midface hypoplasia and elliptocytosis chromosomal region protein 1; Alport syndrome, mental retardation, midface hypoplasia and elliptocytosis chromosomal region gene 1; Alport syndrome, mental retardation, midface hypoplasia and elliptocytosis chromosomal region gene 1 homolog; AMME syndrome candidate gene 1 protein; AMME syndrome candidate gene 1 protein homolog; Ammecr1; AMMERC1
Host Species
Rabbit
Purification Method
Antigen affinity chromatography
Regulatory Status
RUO
Gene ID (Entrez)
9949
Content And Storage
Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.
Form
Liquid
Applications
Immunocytochemistry, Western Blot
Concentration
1 mg/mL
Formulation
0.1M tris glycine with 20% glycerol and 0.01% thimerosal; pH 7
Gene Accession No.
Q9Y4X0
Gene Symbols
AMMECR1
Immunogen
Recombinant protein fragment corresponding to a region within amino acids 107 and 285 of Human AMMECR1
Quantity
100 μL
Primary or Secondary
Primary
Target Species
Human
Product Type
Antibody
Isotype
IgG
Related Products
Description
- Recommended positive controls: 293T, A431, Raji
- Predicted reactivity: Mouse (100%), Zebrafish (95%)
- Store product as a concentrated solution
- Centrifuge briefly prior to opening the vial
- The exact function of this gene is not known, however, submicroscopic deletion of the X chromosome including this gene, COL4A5, and FACL4 genes, result in a contiguous gene deletion syndrome, the AMME complex (Alport syndrome, mental retardation, midface hypoplasia, and elliptocytosis)
- Alternatively spliced transcript variants encoding different isoforms have been found for this gene.