MANSC1 antibody (AA 21-337) (Fluoro594)

Catalog No. ABIN8007784

The Fluoro594-conjugated Rabbit Polyclonal anti-MANSC1 antibody (ABIN8007784) specifically detects MANSC1 in FACS. The antibody is reactive with Human samples.

Quick Overview for MANSC1 antibody (AA 21-337) (Fluoro594) (ABIN8007784)

Target: MANSC1 (MANSC Domain Containing 1 (MANSC1))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This MANSC1 antibody is conjugated to Fluoro594

Application: Flow Cytometry (FACS)

Product Details anti-MANSC1 Antibody (Fluoro594)

Binding Specificity: AA 21-337

Purpose: Anti-MANSC1 Antibody Fluoro594 Conjugated

Cross-Reactivity (Details): No cross-reactivity with other proteins.

Purification: Immunogen affinity purified.

Immunogen: E.coli-derived human MANSC1 recombinant protein (Position: L21-N337).

Isotype: IgG

Application Details

Application Notes: Flow Cytometry, Optimal dilutions should be determined by end users.

Restrictions: For Research Use only

Handling

Format: Liquid

Buffer: Each vial contains 50 % glycerol, 0.9 % NaCl, 0.2 % Na2HPO4, 0.02 % 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: -20 °C

Storage Comment: At -20°C for one year from date of receipt. Avoid repeated freezing and thawing. Protect from light.

Expiry Date: 12 months

Target Details for MANSC1

Target: MANSC1 (MANSC Domain Containing 1 (MANSC1))

Alternative Name: MANSC1

Background:

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.

Gene Full Name: MANSC domain containing 1

Gene ID: 54682

UniProt: Q9H8J5