MANSC1 Polyclonal Antibody
€0.00
In stock
SKU
E-AB-19036
Catalog Number: E-AB-19036
Isotype: Rabbit IgG
Reactivity: human
Applications: IHC,ELISA
Datasheet, Questions? Contact us!
Isotype: Rabbit IgG
Reactivity: human
Applications: IHC,ELISA
Datasheet, Questions? Contact us!
Background:
MANSC1 (MANSC domain-containing protein 1), also known as LOH12CR3 (Loss of heterozygosity 12 chromosomal region 3 protein), is a 414 amino acid single-pass membrane protein. Expressed throughout the body, MANSC1 contains one MANSC domain and is encoded by a gene that is located on chromosome 12. Encoding over 1, 100 genes within 132 million bases, chromosome 12 makes up about 4.5% of the human genome. A number of skeletal deformities are linked to chromosome 12, including hypochondrogenesis, achondrogenesis and Kniest dysplasia. Chromosome 12 is also home to a homeobox gene cluster which encodes crucial transcription factors for morphogenesis, and the natural killer complex gene cluster encoding C-type lectin proteins which mediate the NK cell response to MHC I interaction.
Research Area: Cell Biology
Synonyms:
9130403P13Rik, FLJ10298, LOH12CR3, Loss of heterozygosity 12 chromosomal region 3 protein, MANS1, MANSC domain containing 1, MANSC domain-containing protein 1, MANSC1
Immunogen: Fusion protein of human MANSC1
Swissprot: Q9H8J5
Gene Accession: BC032998
Purification Method: Antigen affinity purification
Buffer: PBS with 0.05% NaN3 and 40% Glycerol, pH7.4
Concentration: 1.8 mg/mL
Dilution: IHC 1:50-1:300, ELISA 1:5000-1:10000
Storage:
Store at -20°C. Avoid freeze / thaw cycles.
MANSC1 (MANSC domain-containing protein 1), also known as LOH12CR3 (Loss of heterozygosity 12 chromosomal region 3 protein), is a 414 amino acid single-pass membrane protein. Expressed throughout the body, MANSC1 contains one MANSC domain and is encoded by a gene that is located on chromosome 12. Encoding over 1, 100 genes within 132 million bases, chromosome 12 makes up about 4.5% of the human genome. A number of skeletal deformities are linked to chromosome 12, including hypochondrogenesis, achondrogenesis and Kniest dysplasia. Chromosome 12 is also home to a homeobox gene cluster which encodes crucial transcription factors for morphogenesis, and the natural killer complex gene cluster encoding C-type lectin proteins which mediate the NK cell response to MHC I interaction.
Research Area: Cell Biology
Synonyms:
9130403P13Rik, FLJ10298, LOH12CR3, Loss of heterozygosity 12 chromosomal region 3 protein, MANS1, MANSC domain containing 1, MANSC domain-containing protein 1, MANSC1
Immunogen: Fusion protein of human MANSC1
Swissprot: Q9H8J5
Gene Accession: BC032998
Purification Method: Antigen affinity purification
Buffer: PBS with 0.05% NaN3 and 40% Glycerol, pH7.4
Concentration: 1.8 mg/mL
Dilution: IHC 1:50-1:300, ELISA 1:5000-1:10000
Storage:
Store at -20°C. Avoid freeze / thaw cycles.
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