GOLGA4 Rabbit Polyclonal Antibody (CAB10216)
- SKU:
- CAB10216
- Product Type:
- Antibody
- Reactivity:
- Human
- Mouse
- Rat
- Host Species:
- Rabbit
- Isotype:
- IgG
- Antibody Type:
- Polyclonal Antibody
- Research Area:
- Cell Biology
Frequently bought together:
Description
Product Name: | GOLGA4 Rabbit Polyclonal Antibody |
SKU: | CAB10216 |
Size: | 20uL, 100uL |
Isotype: | IgG |
Host Species: | Rabbit |
Reactivity: | Human,Mouse,Rat |
Immunogen: | Recombinant fusion protein containing a sequence corresponding to amino acids 1-150 of human GOLGA4 (NP_002069.2). |
Sequence: | MFKK LKQK ISEE QQQL QQAL APAQ ASSN SSTP TRMR SRTS SFTE QLDE GTPN RESG DTQS FAQK LQLR VPSV ESLF RSPI KESL FRSS SKES LVRT SSRE SLNR LDLD SSTA SFDP PSDM DSEA EDLV GNSD SLNK EQLI QRLR RMER SL |
Tested Applications: | WB IHC-P IF/ICC ELISA |
Recommended Dilution: | WB,1:1000 - 1:2000 IHC-P,1:50 - 1:200 IF/ICC,1:50 - 1:200 |
Synonyms: | GCP2; GOLG; p230; CRPF46; MU-RMS-40.18; GOLGA4 |
Positive Sample: | U-87MG,HeLa,SW480,A-549,MCF7,Mouse heart,Mouse brain |
Conjugate: | Unconjugated |
Cellular Localization: | Cytoplasm, Golgi apparatus, Golgi apparatus membrane, Peripheral membrane protein. |
Calculated MW: | 261kDa |
Observed MW: | 280kDa |
The Golgi apparatus, which participates in glycosylation and transport of proteins and lipids in the secretory pathway, consists of a series of stacked cisternae (flattened membrane sacs). Interactions between the Golgi and microtubules are thought to be important for the reorganization of the Golgi after it fragments during mitosis. This gene encodes one of the golgins, a family of proteins localized to the Golgi. This protein has been postulated to play a role in Rab6-regulated membrane-tethering events in the Golgi apparatus. Alternatively spliced transcript variants encoding different isoforms have been identified in this gene.
Purification Method: | Affinity purification |
Gene ID: | 2803 |
Storage Buffer: | Store at -20℃. Avoid freeze / thaw cycles.Buffer: PBS with 0.02% sodium azide,50% glycerol,pH7.3. |