GLT8D1 antibody (Cy3)

Catalog No. ABIN1421267

The Rabbit Polyclonal anti-GLT8D1 antibody is suitable to detect GLT8D1 in samples from Human. It has been validated for IF.

Quick Overview for GLT8D1 antibody (Cy3) (ABIN1421267)

Target: GLT8D1 (Glycosyltransferase 8 Domain Containing 1 (GLT8D1))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This GLT8D1 antibody is conjugated to Cy3

Application: Immunofluorescence (IF)

Product Details anti-GLT8D1 Antibody (Cy3)

Purpose: GLT8D1 Polyclonal Antibody, Cy3 Conjugated

Cross-Reactivity: Human, Mouse, Rat

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human GLT8D1

Isotype: IgG

Application Details

Application Notes: IF(1:100-500)

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, 0.02 % 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: -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 GLT8D1

Target: GLT8D1 (Glycosyltransferase 8 Domain Containing 1 (GLT8D1))

Alternative Name: GLT8D1

Background:

Synonyms: MGC94018, Da2 24, GALA4A, Glycosyltransferase 8 domain containing 1, Glycosyltransferase 8 domain-containing protein 1, Glycosyltransferase AD 017, MSTP139, GL8D1_HUMAN.

Background: GLT8D1 is a 371 amino acid single-pass type II transmembrane protein that is expressed by a gene residing on human chromosome 3. Chromosome 3 is made up of about 214 million bases encoding over 1,100 genes, including a chemokine receptor (CKR) gene cluster and a variety of human cancer-related gene loci. Key tumor suppressing genes on chromosome 3 include those that encode the apoptosis mediator RASSF1, the cell migration regulator HYAL1 and the angiogenesis suppressor SEMA3B. Marfan Syndrome, porphyria, von Hippel-Lindau syndrome, osteogenesis imperfecta and Charcot-Marie-Tooth Disease are a few of the numerous genetic diseases associated with chromosome 3. There are two isoforms of GLT8D1 that are produced as a result of alternative splicing events.

Gene ID: 55830