SCFD2 antibody (AA 20-585)

Catalog No. ABIN7871879

This Rabbit Polyclonal antibody specifically detects SCFD2 in WB, ELISA, FACS and IF. It exhibits reactivity toward Human and Mouse.

Quick Overview for SCFD2 antibody (AA 20-585) (ABIN7871879)

Target: SCFD2 (Sec1 Family Domain Containing 2 (SCFD2))

Reactivity: Human, Mouse

Host: Rabbit

Clonality: Polyclonal

Conjugate: This SCFD2 antibody is un-conjugated

Application: Western Blotting (WB), ELISA, Flow Cytometry (FACS), Immunofluorescence (IF)

Product Details anti-SCFD2 Antibody

Binding Specificity: AA 20-585

Purpose: SCFD2 Antibody / Sec1 family domain-containing protein 2

Purification: Antigen affinity purified

Immunogen: E. coli-derived recombinant human protein (amino acids K20-H585) was used as the immunogen for the SCFD2 antibody.

Isotype: IgG

Application Details

Application Notes: Optimal dilution of the SCFD2 antibody should be determined by the researcher.

Restrictions: For Research Use only

Handling

Format: Lyophilized

Buffer: 0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

Storage: 4 °C,-20 °C

Storage Comment: After reconstitution, the SCFD2 antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.

Target Details for SCFD2

Target: SCFD2 (Sec1 Family Domain Containing 2 (SCFD2))

Alternative Name: SCFD2

Background: SCFD2 (sec1 family domain containing 2), also known as STXBP1L1 (syntaxinbinding protein 1-like 1), is a 684 amino acid protein suggested to play a role in protein transport. Existing as two alternatively spliced isoforms, SCFD2 is a member of the STXBP/unc-18/SEC1 family and is encoded by a gene that maps to human chromosome 4q12. Chromosome 4 represents approximately 6 % of the human genome and contains nearly 900 genes. Notably, the Huntingtin gene, which is found to encode an expanded glutamine tract in cases of Huntingtoni 1/2s disease, is on chromosome 4. FGFR-3 is also encoded on chromosome 4 and has been associated with thanatophoric dwarfism, achondroplasia, Muenke syndrome and bladder cancer. Chromosome 4 is also tied to Ellis-van Creveld syndrome, methylmalonic acidemia and polycystic kidney disease

UniProt: Q8WU76