L2HGDH Rabbit Polyclonal Antibody (CAB15192)
- SKU:
- CAB15192
- Product Type:
- Antibody
- Reactivity:
- Human
- Mouse
- Host Species:
- Rabbit
- Isotype:
- IgG
- Antibody Type:
- Polyclonal Antibody
- Research Area:
- Cell Biology
Frequently bought together:
Description
Product Name: | L2HGDH Rabbit Polyclonal Antibody |
SKU: | CAB15192 |
Size: | 20uL, 100uL |
Isotype: | IgG |
Host Species: | Rabbit |
Reactivity: | Human,Mouse |
Immunogen: | Recombinant fusion protein containing a sequence corresponding to amino acids 1-220 of human L2HGDH (NP_079160.1). |
Sequence: | MVPA LRYL VGAC GRAR GLFA GGSP GACG FASG RPRP LCGG SRSA STSS FDIV IVGG GIVG LASA RALI LRHP SLSI GVLE KEKD LAVH QTGH NSGV IHSG IYYK PESL KAKL CVQG AALL YEYC QQKG ISYK QCGK LIVA VEQE EIPR LQAL YEKG LQNG VPGL RLIQ QEDI KKKE PYCR GLMA IDCP HTGI VDYR QVAL SFAQ DFQE AGGS VLTN FEVK |
Tested Applications: | WB IF/ICC ELISA |
Recommended Dilution: | WB,1:500 - 1:2000 IF/ICC,1:50 - 1:200 |
Synonyms: | L2HGA; C14orf160; L2HGDH |
Positive Sample: | Mouse heart |
Conjugate: | Unconjugated |
Cellular Localization: | Mitochondrion. |
Calculated MW: | 50kDa |
Observed MW: | 50kDa |
This gene encodes L-2-hydroxyglutarate dehydrogenase, a FAD-dependent enzyme that oxidizes L-2-hydroxyglutarate to alpha-ketoglutarate in a variety of mammalian tissues. Mutations in this gene cause L-2-hydroxyglutaric aciduria, a rare autosomal recessive neurometabolic disorder resulting in moderate to severe cognitive disability.
Purification Method: | Affinity purification |
Gene ID: | 79944 |
Storage Buffer: | Store at -20℃. Avoid freeze / thaw cycles.Buffer: PBS with 0.02% sodium azide,50% glycerol,pH7.3. |