HAL polyclonal antibody
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More Files
- More Functions
Western Blot (Tissue lysate)
Western Blot analysis of human fetal liver tissue lysate with HAL polyclonal antibody (Cat # PAB30126) at 1.25 ug/mL working concentration.
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)
Immunohistochemical staining (Formalin-fixed paraffin-embedded sections) of human muscle with HAL polyclonal antibody (Cat # PAB30126) at 4-8 ug/mL working concentration.
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Specification
Product Description
Rabbit polyclonal antibody raised against synthetic peptide of human HAL.
Immunogen
A synthetic peptide corresponding to C-terminus of human HAL.
Sequence
EAAHRLLLEQKVWEVAAPYIEKYRMEHIPESRPLSPTAFSLQFLHKKSTK
Host
Rabbit
Theoretical MW (kDa)
72
Reactivity
Human
Form
Liquid
Purification
Protein A purification
Recommend Usage
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) (4-8 ug/mL)
Western Blot (1.25 ug/mL)
The optimal working dilution should be determined by the end user.Storage Buffer
In PBS (2% sucrose, 0.09% sodium azide).
Storage Instruction
Store at 4°C. For long term storage store at -20°C.
Aliquot to avoid repeated freezing and thawing.Note
This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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Applications
Western Blot (Tissue lysate)
Western Blot analysis of human fetal liver tissue lysate with HAL polyclonal antibody (Cat # PAB30126) at 1.25 ug/mL working concentration.Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)
Immunohistochemical staining (Formalin-fixed paraffin-embedded sections) of human muscle with HAL polyclonal antibody (Cat # PAB30126) at 4-8 ug/mL working concentration. -
Gene Info — HAL
Entrez GeneID
3034GeneBank Accession#
NM_002108Protein Accession#
NP_002099;P42357Gene Name
HAL
Gene Alias
HIS, HSTD
Gene Description
histidine ammonia-lyase
Gene Ontology
HyperlinkGene Summary
Histidine ammonia-lyase is a cytosolic enzyme catalyzing the first reaction in histidine catabolism, the nonoxidative deamination of L-histidine to trans-urocanic acid. Histidine ammonia-lyase defects cause histidinemia which is characterized by increased histidine and histamine and decreased urocanic acid in body fluids [provided by RefSeq
Other Designations
histidase
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Interactome
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Pathway
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Disease
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