HEXA Mouse anti-Human, Clone: AT20F1, Abnova™
Manufacturer: Abnova Corporation
Select a Size
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| Each of 1 | 89-934-239-Each-of-1 | In Stock | ₹ 85,173.00 |
89-934-239 - Each of 1
In Stock
Quantity
1
Base Price: ₹ 85,173.00
GST (18%): ₹ 15,331.14
Total Price: ₹ 1,00,504.14
Antigen
HEXA
Classification
Monoclonal
Conjugate
Unconjugated
Dilution
ELISA Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) (10 ug/mL) Western Blot (1:3000) The optimal working dilution should be determined by the end user.
Gene Alias
MGC99608/TSD
Host Species
Mouse
Purification Method
Protein A purification
Regulatory Status
RUO
Gene ID (Entrez)
3073
Content And Storage
Store at 4°C. For long term storage store at -20°C.Aliquot to avoid repeated freezing and thawing.
Isotype
IgG2a λ
Applications
ELISA, Immunohistochemistry (PFA fixed), Western Blot
Clone
AT20F1
Description
Mouse monoclonal antibody raised against partial recombinant human HEXA.
Formulation
In PBS, pH 7.4 (10% glycerol, 0.02% sodium azide)
Gene Symbols
HEXA
Immunogen
Recombinant protein corresponding to amino acids 89-529 of human HEXA.
Quantity
50 μL
Primary or Secondary
Primary
Target Species
Human
Form
Liquid
Related Products
Description
- This gene encodes the alpha subunit of the lysosomal enzyme beta-hexosaminidase that, together with the cofactor GM2 activator protein, catalyzes the degradation of the ganglioside GM2, and other molecules containing terminal N-acetyl hexosamines
- Beta-hexosaminidase is composed of two subunits, alpha and beta, which are encoded by separate genes
- Both beta-hexosaminidase alpha and beta subunits are members of family 20 of glycosyl hydrolases
- Mutations in the alpha or beta subunit genes lead to an accumulation of GM2 ganglioside in neurons and neurodegenerative disorders termed the GM2 gangliosidoses
- Alpha subunit gene mutations lead to Tay-Sachs disease (GM2-gangliosidosis type I)
- [provided by RefSeq]