ABCC8 Rabbit Polyclonal Antibody (CAB8456)
- SKU:
- CAB8456
- Product Type:
- Antibody
- Applications:
- WB
- Reactivity:
- Mouse
- Host Species:
- Rabbit
- Isotype:
- IgG
- Research Area:
- Signal Transduction
Description
Product Name: | ABCC8 Rabbit Polyclonal Antibody |
SKU: | CAB8456 |
Size: | 20uL, 100uL |
Isotype: | IgG |
Host Species: | Rabbit |
Reactivity: | Mouse |
Immunogen: | Recombinant fusion protein containing a sequence corresponding to amino acids 700-1000 of human ABCC8 (NP_000343.2). |
Sequence: | TIRI PRGQ LTMI VGQV GCGK SSLL LAAL GEMQ KVSG AVFW SSLP DSEI GEDP SPER ETAT DLDI RKRG PVAY ASQK PWLL NATV EENI IFES PFNK QRYK MVIE ACSL QPDI DILP HGDQ TQIG ERGI NLSG GQRQ RISV ARAL YQHA NVVF LDDP FSAL DIHL SDHL MQAG ILEL LRDD KRTV VLVT HKLQ YLPH ADWI IAMK DGTI QREG TLKD FQRS ECQL FEHW KTLM NRQD QELE KETV TERK ATEP PQGL SRAM SSRD GLLQ DEEE EEEE AAES EEDD NLSS MLHQ RAEI PWRA C |
Tested Applications: | WB ELISA |
Recommended Dilution: | WB,1:500 - 1:2000 |
Synonyms: | HI; SUR; HHF1; MRP8; PHHI; SUR1; ABC36; HRINS; PNDM3; TNDM2; SUR1delta2; ABCC8 |
Positive Sample: | Mouse pancreas |
Conjugate: | Unconjugated |
Cellular Localization: | Membrane, Multi-pass membrane protein. |
Calculated MW: | 177kDa |
Observed MW: | 177kDa |
The protein encoded by this gene is a member of the superfamily of ATP-binding cassette (ABC) transporters. ABC proteins transport various molecules across extra- and intra-cellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, White). This protein is a member of the MRP subfamily which is involved in multi-drug resistance. This protein functions as a modulator of ATP-sensitive potassium channels and insulin release. Mutations in the ABCC8 gene and deficiencies in the encoded protein have been observed in patients with hyperinsulinemic hypoglycemia of infancy, an autosomal recessive disorder of unregulated and high insulin secretion. Mutations have also been associated with non-insulin-dependent diabetes mellitus type II, an autosomal dominant disease of defective insulin secretion. Alternatively spliced transcript variants have been found for this gene.
Purification Method: | Affinity purification |
Gene ID: | 6833 |
Storage Buffer: | Store at -20℃. Avoid freeze / thaw cycles.Buffer: PBS with 0.02% sodium azide,50% glycerol,pH7.3. |