EMID1 antibody (AA 351-441) (AbBy Fluor® 680)

Catalog No. ABIN6980834

The Rabbit Polyclonal anti-EMID1 antibody has been validated for IF (cc) and IF (p). It is suitable to detect EMID1 in samples from Rat.

Quick Overview for EMID1 antibody (AA 351-441) (AbBy Fluor® 680) (ABIN6980834)

Target: EMID1 (EMI Domain Containing 1 (EMID1))

Reactivity: Rat

Host: Rabbit

Clonality: Polyclonal

Conjugate: This EMID1 antibody is conjugated to AbBy Fluor® 680

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

Product Details anti-EMID1 Antibody (AbBy Fluor® 680)

Binding Specificity: AA 351-441

Cross-Reactivity: Rat

Predicted Reactivity: Human,Mouse,Dog,Cow

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human EMID1

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 EMID1

Target: EMID1 (EMI Domain Containing 1 (EMID1))

Alternative Name: EMID1

Background:

Synonyms: AW122071, CO 5, CTA-984G1.2, EMI domain containing 1, EMI domain containing protein 1, EMI domain-containing protein 1, EMI5, EMID 1, Emid1, EMID1_HUMAN, Emilin and multimerin domain containing protein 1, Emilin and multimerin domain-containing protein 1, EMU1, hEmu1, MGC50657, OTTMUSP00000005297, Protein Emu1, Putative emu1, RGD1565846, RP23-338J18.3.

Background: Chromosome 22 contains over 500 genes and about 49 million bases. Being the second smallest human chromosome, 22 contains a surprising variety of interesting genes. Phelan-McDermid syndrome, Neurofibromatosis type 2 and autism are associated with chromosome 22. A schizophrenia susceptibility locus has been identified on chromosome 22 and studies show that 22q11 deletion symptoms include a high incidence of schizophrenia. Translocations between chromosomes 9 and 22 may lead to the formation of the Philadelphia Chromosome and the subsequent production of the novel fusion protein, BCR-Abl, a potent cell proliferation activator found in several types of leukemia.

Gene ID: 129080

UniProt: Q96A84