IGSF21 antibody (AA 90-140) (Cy5)

Catalog No. ABIN1419312

This anti-IGSF21 antibody is a Rabbit Polyclonal antibody detecting IGSF21 in WB, IF (p). Suitable for Human, Mouse, Rat.

Quick Overview for IGSF21 antibody (AA 90-140) (Cy5) (ABIN1419312)

Target: IGSF21 (Immunoglobin Superfamily, Member 21 (IGSF21))

Reactivity: Human, Mouse, Rat

Host: Rabbit

Clonality: Polyclonal

Conjugate: This IGSF21 antibody is conjugated to Cy5

Application: Western Blotting (WB), Immunofluorescence (Paraffin-embedded Sections) (IF (p))

Product Details anti-IGSF21 Antibody (Cy5)

Binding Specificity: AA 90-140

Cross-Reactivity: Human, Mouse, Rat

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human IGSF21

Isotype: IgG

Application Details

Application Notes: IF(IHC-P) 1:50-200

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 1 μg/μL

Buffer: Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.

Preservative: ProClin

Precaution of Use: This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.

Storage: -20 °C

Storage Comment: Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

Expiry Date: 12 months

Target Details for IGSF21

Target: IGSF21 (Immunoglobin Superfamily, Member 21 (IGSF21))

Alternative Name: IGSF21

Background:

Synonyms: FLJ41177, IGSF 21, Immunoglobin superfamily member 21, immunoglobulin superfamily member 21, MGC15730, RP11 121A23.1, IGS21_HUMAN, IgSF21

Background: IGSF21 is a 467 amino acid secreted protein that contains two Ig-like (immunoglobulin-like) domains and is a member of the immunoglobulin superfamily. Members of this family of proteins usually localize to the cell membrane, and may act as receptors in the immune response pathways. The gene encoding IGSF21 maps to human chromosome 1p36.13 and mouse chromosome 4 D3. Human chromosome 1 spans 260 million base pairs, contains over 3,000 genes and comprises nearly 8 % of the human genome. A large number of disease-associated genes are associated with chromosome 1, including those that are involved in familial adenomatous polyposis, Stickler syndrome, Parkinson?s disease, Gaucher disease, schizophrenia and Usher syndrome. Aberrations in chromosome 1 are found in a variety of cancers, including head and neck cancer, malignant melanoma and multiple myeloma.

Gene ID: 84966

UniProt: Q96ID5