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The antibody against KIF6 was raised in Rabbit using the recombinant fusion protein containing a sequence corresponding to amino acids 565-814 of human KIF6 (NP_659464.3) as the immunogen. The polyclonal antibody exists as a isotype IgG, by affinity purification. This antibody has been validated on WB, ELISA.
The antibody against KIF6 was raised in Rabbit using the recombinant fusion protein containing a sequence corresponding to amino acids 565-814 of human KIF6 (NP_659464.3) as the immunogen. The polyclonal antibody exists as a isotype IgG, by affinity purification. This antibody has been validated on WB, ELISA.
| Cat.No | ADA-02400A | Clonality | Polyclonal |
|---|---|---|---|
| Host Species | Rabbit | Target Name | KIF6 |
| Target Synonyms | C6orf102; dJ137F1.4; dJ188D3.1; dJ1043E3.1; KIF6 | Form | Liquid |
| Species Reactivity | Human, Mouse | Isotype | IgG |
| Storage Buffer | 50% Glycerol, PBS with 0.02% sodium azide, pH7.3. | Purification Method | Affinity purification |
| Positive Samples | Mouse testis | Application | ELISA, WB |
| Immunogen Description | Recombinant fusion protein containing a sequence corresponding to amino acids 565-814 of human KIF6 (NP_659464.3). | Target Species | Human |
|---|---|---|---|
| Uniprot ID | Q6ZMV9 | Immunogen Sequence |
Uniprot Id
Q6ZMV9
Target Species
Human
Target Name
KIF6
Target Full Name
Kinesin-like protein KIF6
Target Subcellular Location
Cytoplasm, cytoskeleton.
Target Protein Families
TRAFAC class myosin-kinesin ATPase superfamily, Kinesin family
Target Synonyms
KIF6; C6orf102Kinesin-like protein KIF6
Target Background
This gene encodes a member of a family of molecular motors which are involved in intracellular transport of protein complexes, membrane organelles, and messenger ribonucleic acid along microtubules. Kinesins function as homodimeric molecules with two N-terminal head domains that move along microtubules and two C-terminal tail domains that interact with the transported cargo, either directly or indirectly, through adapter molecules. This gene is ubiquitously expressed in coronary arteries and other vascular tissue. A naturally occurring mutation in this gene is associated with coronary heart disease.
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