NDUFS4 Monoclonal Antibody (CAB22056)
- SKU:
- CAB22056
- Product Type:
- Antibody
- Antibody Type:
- Monoclonal Antibody
- Reactivity:
- Human
- Mouse
- Rat
- Host Species:
- Rabbit
- Isotype:
- IgG
- Applications:
- WB
Frequently bought together:
Description
Product Name: | NDUFS4 Monoclonal Antibody |
SKU: | CAB22056 |
Size: | 20uL, 100uL |
Isotype: | IgG |
Host Species: | Rabbit |
Reactivity: | Human,Mouse,Rat |
Immunogen: | Recombinant fusion protein containing a sequence corresponding to amino acids 43-175 of human NDUFS4 (NP_002486.1). |
Sequence: | AQDQ TQDT QLIT VDEK LDIT TLTG VPEE HIKT RKVR IFVP ARNN MQSG VNNT KKWK MEFD TRER WENP LMGW ASTA DPLS NMVL TFST KEDA VSFA EKNG WSYD IEER KVPK PKSK SYGA NFSW NKRT RVST K |
Tested Applications: | WB ELISA |
Recommended Dilution: | WB,1:2000 - 1:20000 |
Synonyms: | AQDQ; CI-18; MC1DN1; CI-AQDQ; CI-18 kDa; NDUFS4 |
Positive Sample: | K-562,A-431,Mouse brain,Mouse heart,Rat brain |
Conjugate: | Unconjugated |
Cellular Localization: | Matrix side, Mitochondrion inner membrane, Peripheral membrane protein. |
Calculated MW: | 20kDa |
Observed MW: | 20kDa |
This gene encodes a nuclear-encoded accessory subunit of the mitochondrial membrane respiratory chain NADH dehydrogenase (complex I, or NADH:ubiquinone oxidoreductase). Complex I removes electrons from NADH and passes them to the electron acceptor ubiquinone. Mutations in this gene can cause mitochondrial complex I deficiencies such as Leigh syndrome. Alternative splicing results in multiple transcript variants.
Purification Method: | Affinity purification |
Gene ID: | 4724 |
Clone Number: | ARC54574 |
Storage Buffer: | Store at -20℃. Avoid freeze / thaw cycles.Buffer: PBS with 0.05% proclin300,0.05% BSA,50% glycerol,pH7.3. |