AFG3L2 Polyclonal Antibody (CAB23598)
- SKU:
- CAB23598
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Description
| Product Name: | AFG3L2 Polyclonal Antibody |
| SKU: | CAB23598 |
| Size: | 20uL, 100uL |
| Isotype: | IgG |
| Host Species: | Rabbit |
| Reactivity: | Human,Mouse,Rat |
| Immunogen: | Recombinant fusion protein containing a sequence corresponding to amino acids 538-797 of human AFG3L2（NP_006787.2）. |
| Sequence: | DSIN QKHF EQAI ERVI GGLE KKTQ VLQP EEKK TVAY HEAG HAVA GWYL EHAD PLLK VSII PRGK GLGY AQYL PKEQ YLYT KEQL LDRM CMTL GGRV SEEI FFGR ITTG AQDD LRKV TQSA YAQI VQFG MNEK VGQI SFDL PRQG DMVL EKPY SEAT ARLI DDEV RILI NDAY KRTV ALLT EKKA DVEK VALL LLEK EVLD KNDM VELL GPRP FAEK STYE EFVE GTGS LDED TSLP EGLK DWNK EREK EKEE PPGE KVAN |
| Tested Applications: | WB IHC-P IP ELISA |
| Recommended Dilution: | WB,1:500 - 1:1000 IHC-P,1:50 - 1:200 IP,0.5μg-4μg antibody for 400μg-600μg extracts of whole cells |
| Synonyms: | OPA12; SCA28; SPAX5; AFG3L2 |
| Positive Sample: | Jurkat,293T,Mouse liver |
| Conjugate: | Unconjugated |
| Cellular Localization: | Mitochondrion membrane, Multi-pass membrane protein. |
| Calculated MW: | 89kDa |
| Observed MW: | 80kDa |
This gene encodes a protein localized in mitochondria and closely related to paraplegin. The paraplegin gene is responsible for an autosomal recessive form of hereditary spastic paraplegia. This gene is a candidate gene for other hereditary spastic paraplegias or neurodegenerative disorders.
| Purification Method: | Affinity purification |
| Gene ID: | 10939 |
| Storage Buffer: | Store at -20℃. Avoid freeze / thaw cycles.Buffer: PBS with 0.05% proclin300,50% glycerol,pH7.3. |
 | Western blot analysis of various lysates, using AFG3L2 Rabbit pAb (CAB23598) at 1:1000 dilution.Secondary antibody: HRP Goat Anti-Rabbit IgG (H+L) (CABS014) at 1:10000 dilution.Lysates/proteins: 25μg per lane.Blocking buffer: 3% nonfat dry milk in TBST.Detection: ECL Basic Kit (AbGn00020).Exposure time: 60s. |
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