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ELK Biotechnology
SKU:ES18360
ANAG rabbit pAb
ANAG rabbit pAb
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$250.00 USD
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Applications: WB
Reactivity: Human;Rat;Mouse;
Source: Rabbit
Dilution: WB 1：500-2000
Immunogen: Synthesized peptide derived from human ANAG AA range: 146-196
Storage_stability: -20°C/1 year
Clonality: Polyclonal
Isotype: IgG
Concentration: 1 mg/ml
Human_gene_id: 4669
Human_swiss_prot_no: P54802
Subcellular_location: Lysosome.
Background: This gene encodes an enzyme that degrades heparan sulfate by hydrolysis of terminal N-acetyl-D-glucosamine residues in N-acetyl-alpha-D-glucosaminides. Defects in this gene are the cause of mucopolysaccharidosis type IIIB (MPS-IIIB), also known as Sanfilippo syndrome B. This disease is characterized by the lysosomal accumulation and urinary excretion of heparan sulfate. [provided by RefSeq, Jul 2008],
Reactivity: Human;Rat;Mouse;
Source: Rabbit
Dilution: WB 1：500-2000
Immunogen: Synthesized peptide derived from human ANAG AA range: 146-196
Storage_stability: -20°C/1 year
Clonality: Polyclonal
Isotype: IgG
Concentration: 1 mg/ml
Human_gene_id: 4669
Human_swiss_prot_no: P54802
Subcellular_location: Lysosome.
Background: This gene encodes an enzyme that degrades heparan sulfate by hydrolysis of terminal N-acetyl-D-glucosamine residues in N-acetyl-alpha-D-glucosaminides. Defects in this gene are the cause of mucopolysaccharidosis type IIIB (MPS-IIIB), also known as Sanfilippo syndrome B. This disease is characterized by the lysosomal accumulation and urinary excretion of heparan sulfate. [provided by RefSeq, Jul 2008],
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