PIPA5109768
GLB1L3 Polyclonal Antibody, Invitrogen™
Manufacturer: Thermo Scientific
Select a Size
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| Each of 1 | PIPA5109768-Each-of-1 | In Stock | ₹ 46,502.50 |
PIPA5109768 - Each of 1
In Stock
Quantity
1
Base Price: ₹ 46,502.50
GST (18%): ₹ 8,370.45
Total Price: ₹ 54,872.95
Antigen
GLB1L3
Classification
Polyclonal
Conjugate
Unconjugated
Gene
GLB1L3
Gene Alias
4921509F24Rik; beta-galactosidase-1-like protein 3; galactosidase beta 1 like 3; galactosidase beta 1-like 3; galactosidase, beta 1 like 3; galactosidase, beta 1-like 3; GLB1L3
Host Species
Rabbit
Purification Method
Affinity Chromatography
Regulatory Status
RUO
Gene ID (Entrez)
112937, 500961, 70893
Content And Storage
-20° C, Avoid Freeze/Thaw Cycles
Form
Liquid
Applications
Western Blot
Concentration
0.53 mg/mL
Formulation
PBS with 50% glycerol and 0.01% thimerosal; pH 7.3
Gene Accession No.
A2RSQ1, Q5XIL5, Q8NCI6
Gene Symbols
GLB1L3
Immunogen
Recombinant fusion protein containing a sequence corresponding to amino acids 180-290 of human GLB1L3 (NP_001073876.2).
Quantity
100 μL
Primary or Secondary
Primary
Target Species
Human, Mouse, Rat
Product Type
Antibody
Isotype
IgG
Related Products
Description
- Immunogen sequence: QDPRLLLRTT NKSFIEAVEK YFDHLIPRVI PLQYRQAGPV IAVQVENEYG SFNKDKTYMP YLHKALLRRG IVELLLTSDG EKHVLSGHTK GVLAAINLQK LHQDTFNQLH K GLB1L3 (beta-galactosidase-1-like protein 3) is a 653 amino acid protein belonging to the glycosyl hydrolase 35 family
- GLB1L3 exists as three alternatively spliced isoforms and is encoded by a gene that maps to human chromosome 11q25
- With approximately 135 million base pairs and 1,400 genes, chromosome 11 makes up around 4% of human genomic DNA and is considered a gene and disease association dense chromosome
- The chromosome 11 encoded Atm gene is important for regulation of cell cycle arrest and apoptosis following double strand DNA breaks
- Atm mutation leads to the disorder known as ataxia-telangiectasia
- Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are also associated with defects in chromosome 11.