EMID1 antibody (AA 351-441)

Catalog No. ABIN6943246

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

Quick Overview for EMID1 antibody (AA 351-441) (ABIN6943246)

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

Reactivity: Rat

Host: Rabbit

Clonality: Polyclonal

Conjugate: This EMID1 antibody is un-conjugated

Application: ELISA, Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunohistochemistry (Frozen Sections) (IHC (fro)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunocytochemistry (ICC)

Product Details anti-EMID1 Antibody

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: ELISA 1:500-1000
IHC-P 1:200-400
IHC-F 1:100-500
IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200
ICC 1:100-500

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 1 μg/μL

Buffer: 0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % 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: 4 °C,-20 °C

Storage Comment: Shipped at 4°C. Store at -20°C for one year. 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