GLT8D2 antibody (AA 85-180) (AbBy Fluor® 488)
-
- Target See all GLT8D2 Antibodies
- GLT8D2 (Glycosyltransferase 8 Domain Containing 2 (GLT8D2))
-
Binding Specificity
- AA 85-180
-
Reactivity
- Human
-
Host
- Rabbit
-
Clonality
- Polyclonal
-
Conjugate
- This GLT8D2 antibody is conjugated to AbBy Fluor® 488
-
Application
- Western Blotting (WB), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunofluorescence (Cultured Cells) (IF (cc))
- 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
- Top Product
- Discover our top product GLT8D2 Primary Antibody
-
-
- Application Notes
-
IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200 - Restrictions
- For Research Use only
-
- 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
- GLT8D2 (Glycosyltransferase 8 Domain Containing 2 (GLT8D2))
- Alternative Name
- GLT8D2 (GLT8D2 Products)
- Synonyms
- si:dkey-22l11.1 antibody, zgc:136873 antibody, 1110021D20Rik antibody, RGD1560432 antibody, glycosyltransferase 8 domain containing 2 antibody, GLT8D2 antibody, glt8d2 antibody, Glt8d2 antibody
- 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
-