GLT8D2 antibody (AA 85-180) (Biotin)

Catalog No. ABIN1398307

This Rabbit Polyclonal antibody specifically detects GLT8D2 in WB, ELISA, IHC (fro) and IHC (p). It exhibits reactivity toward Human.

Quick Overview for GLT8D2 antibody (AA 85-180) (Biotin) (ABIN1398307)

Target: GLT8D2 (Glycosyltransferase 8 Domain Containing 2 (GLT8D2))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This GLT8D2 antibody is conjugated to Biotin

Application: Western Blotting (WB), ELISA, Immunohistochemistry (Frozen Sections) (IHC (fro)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Product Details anti-GLT8D2 Antibody (Biotin)

Binding Specificity: AA 85-180

Cross-Reactivity: Human

Predicted Reactivity: Mouse,Rat,Dog,Cow,Horse,Rabbit

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human GLT8D2

Isotype: IgG

Application Details

Application Notes: WB 1:300-5000
IHC-P 1:200-400
IHC-F 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, 0.03 % 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 for 12 months.

Expiry Date: 12 months

Target Details for GLT8D2

Target: GLT8D2 (Glycosyltransferase 8 Domain Containing 2 (GLT8D2))

Alternative Name: GLT8D2

Background:

Synonyms: GALA4A, GL8D2_HUMAN, GLT8D2, Glycosyltransferase 8 domain containing 2, Glycosyltransferase 8 domain-containing protein 2, Gycosyltransferase.

Background: GLT8D2 (glycosyltransferase 8 domain-containing protein 2), also known as GALA4A, is a 349 amino acid single-pass type II membrane protein. A member of the glycosyltransferase 8 family, GLT8D2 is encoded by a gene that maps to human chromosome 12q23.3. Encoding over 1,100 genes within 132 million base pairs, chromosome 12 makes up about 4.5 % of the human genome. A number of skeletal deformities are linked to chromosome 12, including hypochondrogenesis, achondrogenesis, Noonan syndrome, Kniest dysplasia and trisomy 12p. Chromosome 12 is also home to a homeobox gene cluster, which encodes crucial transcription factors for morphogenesis, as well as the natural killer complex gene cluster, which encodes C-type lectin proteins that mediate the NK cell response to MHC I interaction.

Gene ID: 83468