SOX9 Rabbit Monoclonal Antibody (CAB19710)
- SKU:
- CAB19710
- Product Type:
- Antibody
- Reactivity:
- Human
- Mouse
- Rat
- Host Species:
- Rabbit
- Isotype:
- IgG
- Research Area:
- Epigenetics and Nuclear Signaling
Frequently bought together:
Description
Product Name: | SOX9 Rabbit Monoclonal Antibody |
SKU: | CAB19710 |
Size: | 20uL, 100uL |
Isotype: | IgG |
Host Species: | Rabbit |
Reactivity: | Human,Mouse,Rat |
Immunogen: | Recombinant fusion protein containing a sequence corresponding to amino acids 169-300 of human SOX9 (P48436). |
Sequence: | HPDY KYQP RRRK SVKN GQAE AEEA TEQT HISP NAIF KALQ ADSP HSSS GMSE VHSP GEHS GQSQ GPPT PPTT PKTD VQPG KADL KREG RPLP EGGR QPPI DFRD VDIG ELSS DVIS NIET FDVN EFDQ YLPP |
Tested Applications: | WB IHC-P IF/ICC IP ELISA |
Recommended Dilution: | WB,1:500 - 1:2000 IHC-P,1:100 - 1:500 IF/ICC,1:50 - 1:200 IP,0.5μg-4μg antibody for 200μg-400μg extracts of whole cells |
Synonyms: | CMD1; SRA1; CMPD1; SRXX2; SRXY10; SOX9 |
Positive Sample: | Hep G2,HeLa |
Conjugate: | Unconjugated |
Cellular Localization: | Nucleus. |
Calculated MW: | 56kDa |
Observed MW: | 56kDa |
The protein encoded by this gene recognizes the sequence CCTTGAG along with other members of the HMG-box class DNA-binding proteins. It acts during chondrocyte differentiation and, with steroidogenic factor 1, regulates transcription of the anti-Muellerian hormone (AMH) gene. Deficiencies lead to the skeletal malformation syndrome campomelic dysplasia, frequently with sex reversal.
Purification Method: | Affinity purification |
Gene ID: | 6662 |
Clone Number: | ARC0190 |
Storage Buffer: | Store at -20℃. Avoid freeze / thaw cycles.Buffer: PBS with 0.02% sodium azide,0.05% BSA,50% glycerol,pH7.3. |