GBA Polyclonal Antibody
| Code | Size | Price |
|---|
| E-AB-19899-20uL | 20uL | £125.00 |
Quantity:
| E-AB-19899-60uL | 60uL | £172.00 |
Quantity:
| E-AB-19899-120uL | 120uL | £237.00 |
Quantity:
| E-AB-19899-200uL | 200uL | £344.00 |
Quantity:
Prices exclude any Taxes / VAT
Overview
Host Type: Rabbit
Antibody Isotype: IgG
Antibody Clonality: Polyclonal
Regulatory Status: RUO
Target Species:
- Human
- Mouse
Applications:
- Enzyme-Linked Immunosorbent Assay (ELISA)
- Immunohistochemistry (IHC)
- Western Blot (WB)
Shipping:
Ice packs
Storage:
Store at -20°C. Avoid freeze / thaw cycles.
Further Information
Abbreviation:
GBA
Background:
This gene encodes a lysosomal membrane protein that cleaves the beta-glucosidic linkage of glycosylceramide, an intermediate in glycolipid metabolism. Mutations in this gene cause Gaucher disease, a lysosomal storage disease characterized by an accumulation of glucocerebrosides. A related pseudogene is approximately 12 kb downstream of this gene on chromosome 1. Alternative splicing results in multiple transcript variants.
Buffer:
PBS with 0.05% NaN3 and 40% Glycerol,pH7.4
Calculated MW:
60 kDa
Concentration:
1.56 mg/mL
Conjugation:
Unconjugated
Dilution:
WB 1:500-1:2000, IHC 1:50-1:100, ELISA 1:5000-1:10000
Immunogen:
Synthetic peptide of human GBA
ObservedMW:
Refer to figures
Purification method:
Antigen affinity purification
Target Synonym:
Acid beta glucosidase;Acid beta-glucosidase;Alglucerase;Beta glucocerebrosidase;BETA GLUCOSIDASE; ACID;Beta-glucocerebrosidase;betaGC;D glucosyl N acylsphingosine glucohydrolase;D-glucosyl-N-acylsphingosine glucohydrolase;EC 3.2.1.45 ;GBA;Gba protein ;GBA1;GC;GCase;GCB;GLCM;GLUC;Glucocerebrosidase (alt.) ;Glucocerebrosidase;GLUCOCEREBROSIDASE PSEUDOGENE;Glucosidase beta;Glucosidase; beta; acid;Glucosidase; beta; acid (includes glucosylceramidase);Glucosylceramidase;Imiglucerase;Lysosomal glucocerebrosidase ;OTTHUMP00000033992;OTTHUMP00000033993
UNIProt ID:
P04062