[KO Validated] NSDHL Rabbit Polyclonal Antibody (CAB16893)
- SKU:
- CAB16893
- Product Type:
- Antibody
- Reactivity:
- Human
- Mouse
- Rat
- Host Species:
- Rabbit
- Isotype:
- IgG
- Antibody Type:
- Polyclonal Antibody
- Research Area:
- Metabolism
Frequently bought together:
Description
Product Name: | [KO Validated] NSDHL Rabbit Polyclonal Antibody |
SKU: | CAB16893 |
Size: | 20uL, 100uL |
Isotype: | IgG |
Host Species: | Rabbit |
Reactivity: | Human,Mouse,Rat |
Immunogen: | Recombinant fusion protein containing a sequence corresponding to amino acids 1-240 of human NSDHL (NP_057006.1). |
Sequence: | MEPA VSEP MRDQ VART HLTE DTPK VNAD IEKV NQNQ AKRC TVIG GSGF LGQH MVEQ LLAR GYAV NVFD IQQG FDNP QVRF FLGD LCSR QDLY PALK GVNT VFHC ASPP PSSN NKEL FYRV NYIG TKNV IETC KEAG VQKL ILTS SASV IFEG VDIK NGTE DLPY AMKP IDYY TETK ILQE RAVL GAND PEKN FLTT AIRP HGIF GPRD PQLV PILI EAAR NGKM KFVI GNGK NLVD FTFV |
Tested Applications: | WB IHC-P IF/ICC ELISA |
Recommended Dilution: | WB,1:500 - 1:1000 IHC-P,1:50 - 1:200 IF/ICC,1:50 - 1:200 |
Synonyms: | H105E3; XAP104; SDR31E1; HL |
Positive Sample: | 293T |
Cellular Localization: | endoplasmic reticulum, lipid droplet |
Calculated MW: | 42kDa |
Observed MW: | 40kDa |
The protein encoded by this gene is localized in the endoplasmic reticulum and is involved in cholesterol biosynthesis. Mutations in this gene are associated with CHILD syndrome, which is a X-linked dominant disorder of lipid metabolism with disturbed cholesterol biosynthesis, and typically lethal in males. Alternatively spliced transcript variants with differing 5' UTR have been found for this gene.
Purification Method: | Affinity purification |
Gene ID: | 50814 |
Storage Buffer: | Store at -20℃. Avoid freeze / thaw cycles.Buffer: PBS with 0.01% thimerosal,50% glycerol,pH7.3. |