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Astor Scientific  |  SKU: ASTP8725

Human ARL6 (Adp-Ribosylation Factor-Like Protein 6) - Recombinant Protein

Molecule: ARL6
Species: Human
Expression System: E.coli
Tag: N-6His
Expression Range: 1-186aa
$429.99 $549.99
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SDS-PAGE analysis of Human ARL6 (Adp-Ribosylation Factor-Like Protein 6) - Recombinant Protein, showing >95% purity under 15% SDS-PAGE (Reduced)
Astor Scientific

Human ARL6 (Adp-Ribosylation Factor-Like Protein 6) - Recombinant Protein

$429.99 $549.99

Product Overview

Product Name Recombinant Human ARL6 Protein
Product Overview This recombinant human ARL6 protein includes amino acids 1-186aa of the target gene is expressed in E.coli.The protein is supplied in lyophilized form and formulated in phosphate buffered saline (pH7.4) containing 0.01% sarcosyl, 5% trehaloseprior to lyophilization.
Target Uniprot Id Q9H0F7
Recommended Name ADP-ribosylation factor-like protein 6
Gene Name ARL6
Synonyms ADP-ribosylation factor-like protein 6, BBS3, MGC32934, RP55
Species Human
Predicted Molecular Mass 23.2 kDa
Expression System E.coli
Expression Range 1-186aa
Tag N-6His
Purity >95%
Formulation Lyophilized
Buffer Phosphate buffered saline (pH7.4) containing 0.01% sarcosyl, 5%Trehalose
Storage Condition 1. Store at -20°C/-80°C upon receipt, aliquoting is necessary for mutiple use. 2. Avoid repeated freeze-thaw cycles. 3. Store working aliquots at 4°C for up to one week. 4. In general, protein in liquid form is stable for up to 6 months at -20°C/-80°C. Protein in lyophilized powder form is stable for up to 12 months at -20°C/-80°C.
Reconstitution Instruction Briefly centrifuged the vial prior to opening to bring the contents to the bottom. Reconstitute protein in deionized sterile water to a concentration of 0.1-1.0 mg/mL. It is recommended to add 5-50% of glycerol (final concentration) and aliquot for long-term storage at -20°C/-80°C. The default final concentration of glycerol is 50%.
Applications Positive Control; Immunogen; SDS-PAGE; WB
Research Area Signal Transduction
Target Function Involved in membrane protein trafficking at the base of the ciliary organelle. Mediates recruitment onto plasma membrane of the BBSome complex which would constitute a coat complex required for sorting of specific membrane proteins to the primary cilia. Together with BBS1, is necessary for correct trafficking of PKD1 to primary cilia. Together with the BBSome complex and LTZL1, controls SMO ciliary trafficking and contributes to the sonic hedgehog (SHH) pathway regulation. May regulate cilia assembly and disassembly and subsequent ciliary signaling events such as the Wnt signaling cascade. Isoform 2 may be required for proper retinal function and organization.
Subcellular Location Cell projection, cilium membrane; Peripheral membrane protein; Cytoplasmic side. Cytoplasm, cytoskeleton, cilium axoneme. Cytoplasm, cytoskeleton, cilium basal body. Note=Appears in a pattern of punctae flanking the microtubule axoneme that likely correspond to small membrane-associated patches. Localizes to the so-called ciliary gate where vesicles carrying ciliary cargo fuse with the membrane.
Protein Family Small GTPase superfamily, Arf family
Associated Diseases Bardet-Biedl syndrome 3 (BBS3); Retinitis pigmentosa 55 (RP55)

Size

  • 100ug
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