PIMA531036
Arylsulfatase A Recombinant Rabbit Monoclonal Antibody (001), Invitrogen™
Manufacturer: Thermo Scientific
Select a Size
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| Each of 1 | PIMA531036-Each-of-1 | In Stock | ₹ 41,385.00 |
PIMA531036 - Each of 1
In Stock
Quantity
1
Base Price: ₹ 41,385.00
GST (18%): ₹ 7,449.30
Total Price: ₹ 48,834.30
Antigen
Arylsulfatase A
Classification
Recombinant Monoclonal
Concentration
1 mg/mL
Formulation
PBS with no preservative
Gene Accession No.
P50428
Gene Symbols
ARSA
Immunogen
Recombinant Mouse Arylsulfatase A/ARSA protein (Met1-Ser506)
Quantity
100 μL
Primary or Secondary
Primary
Target Species
Mouse
Product Type
Antibody
Isotype
IgG
Applications
ELISA
Clone
001
Conjugate
Unconjugated
Gene
ARSA
Gene Alias
ARSA; ARSA1; ARSA-I; Arylsulfatase A; Arylsulfatase A component B; Arylsulfatase A component C; As2; As-2; ASA; AS-A; ASNA-I; ATPase ASNA1; AW212749; cerebroside-sulfatase; EC 3.1.6.8; GET3; hASNA-I; MLD; TISP73; TRC40
Host Species
Rabbit
Purification Method
Protein A
Regulatory Status
RUO
Gene ID (Entrez)
11883
Content And Storage
Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.
Form
Liquid
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Description
- This product is preservative free
- It is recommended to add sodium azide to avoid contamination (final concentration 0.05%-0.1%)
- Recombinant rabbit monoclonal antibodies are produced using in vitro expression systems
- The expression systems are developed by cloning in the specific antibody DNA sequences from immunoreactive rabbits
- Then, individual clones are screened to select the best candidates for production
- The advantages of using recombinant rabbit monoclonal antibodies include: better specificity and sensitivity, lot-to-lot consistency, animal origin-free formulations, and broader immunoreactivity to diverse targets due to larger rabbit immune repertoire
- This antibody has specificity for Mouse Arylsulfatase A/ARSA
- The protein encoded by this gene hydrolyzes cerebroside sulfate to cerebroside and sulfate
- Defects in this gene lead to metachromatic leucodystrophy, a progressive demyelination disease which results in a variety of neurological symptoms and μgtimately death
- Alternatively spliced transcript variants have been described for this gene.