GIMAP7 antibody (AA 1-100) (FITC)

Catalog No. ABIN898916

The Rabbit Polyclonal anti-GIMAP7 antibody has been validated for IF (cc) and IF (p). It is suitable to detect GIMAP7 in samples from Human.

Quick Overview for GIMAP7 antibody (AA 1-100) (FITC) (ABIN898916)

Target: GIMAP7 (GTPase, IMAP Family Member 7 (GIMAP7))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This GIMAP7 antibody is conjugated to FITC

Application: Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))

Product Details anti-GIMAP7 Antibody (FITC)

Binding Specificity: AA 1-100

Predicted Reactivity: Human

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human GIMAP7

Isotype: IgG

Application Details

Application Notes: IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 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 GIMAP7

Target: GIMAP7 (GTPase, IMAP Family Member 7 (GIMAP7))

Alternative Name: GIMAP7

Background:

Synonyms: GTPase IMAP family member 7, hIAN7, IAN 7, IAN7, Immune associated nucleotide, immunity associated nucleotide 7 protein, MGC27027, GIMA7_HUMAN.

Background: The GTPase of the immunity-associated protein (GIMAP) family of proteins include seven members that are expressed by genes residing on human chromosome 7. GIMAP proteins have been implicated in the regulation of lymphomyeloid cell survival. GIMAP7 (GTPase IMAP family member 7), also known as IAN7 (immunity-associated nucleotide 7), is a 300 amino acid protein encoded by a gene that maps to human chromosome 7q36.1. Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterized by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia.

Gene ID: 168537