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Arylsulfatase A antibody (C-Term)
ARSA
Reactivity: Human
WB
Host: Mouse
Monoclonal
498CT24-1-2
unconjugated
Product Details anti-Arylsulfatase A Antibody
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Target
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Arylsulfatase A (ARSA)
Binding Specificity
All epitopes for Arylsulfatase A antibodies
AA 408-439, C-Term
Reactivity
All reactivities for Arylsulfatase A antibodies
Human
Host
All hosts for Arylsulfatase A antibodies
Mouse
Clonality
All clonalities for Arylsulfatase A antibodies
Monoclonal
Conjugate
All conjugates for Arylsulfatase A antibodies
This Arylsulfatase A antibody is un-conjugated
Application
All applications for Arylsulfatase A antibodies
Western Blotting (WB)
Purification
This antibody is purified through a protein G column, followed by dialysis against PBS.
Immunogen
This ARSA antibody is generated from mice immunized with a KLH conjugated synthetic peptide between 408-439 amino acids from the C-terminal region of human ARSA.
Clone
498CT24-1-2
Isotype
IgG2a
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Discover our top product ARSA Primary Antibody
Alternatives
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Application Details
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Application Notes
WB: 1:100~250
Restrictions
For Research Use only
Handling
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Format
Liquid
Buffer
Purified monoclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.
Preservative
Sodium azide
Precaution of Use
This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
Storage
4 °C,-20 °C
Storage Comment
ARSA Antibody (C-term) can be refrigerated at 2-8 °C for up to 6 months. For long term storage, keep at -20 °C.
Expiry Date
6 months
Target Details for Arylsulfatase A
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Target
Arylsulfatase A (ARSA)
Alternative Name
ARSA (ARSA Products )
Synonyms
ARSA antibody, zgc:101575 antibody, arsa antibody, AS-A antibody, ASA antibody, AW212749 antibody, As-2 antibody, As2 antibody, TISP73 antibody, MLD antibody, mld antibody, arylsulfatase A antibody, arylsulfatase antibody, arylsulfatase A, gene 1 S homeolog antibody, ARSA antibody, arsa antibody, arsA antibody, RB6599 antibody, Arsa antibody, arsa.1.S antibody
Background
The protein encoded by this gene hydrolyzes cerebroside sulfate to cerebroside and sulfate. Defects in this gene lead to metachromatic leucodystrophy (MLD), a progressive demyelination disease which results in a variety of neurological symptoms and ultimately death. Alternatively spliced transcript variants have been described for this gene.
Molecular Weight
53588
Gene ID
410
NCBI Accession
NP_000478 , NP_001078894 , NP_001078895 , NP_001078896 , NP_001078897
UniProt
P15289
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