Recombinant humaan B9D1-eiwit

BpD1 is a B9 domain-containing protein, one of several that are involved in ciliogenesis. Alterations in expression of this gene have been found in a family with Meckel syndrome. Meckel syndrome has been associated with at least six different genes. This gene is located within the Smith-Magenis syndrome region on chromosome 17. Three alternatively spliced transcript variants that encode different proteins have been described for this gene. Recombinant human B9D1 protein, used to His-tag at N-terminus, was expressed in E. coli.

B9 domain-containing protein 1 isoform b, B9, EPPB9, MKS9, MKSR1

E.coli

Human

His-Tag

SDS-PAGE, Denatured

1 mg/mL (determined by Bradford assay)

> 85% by SDS-PAGE

25.2 kDa (227aa)

B9D1, B9 domain-containing protein 1 isoform b, B9, EPPB9, MKS9, MKSR1, ATGP2803-10 µg, ATGP2803-20 µg, ATGP2803-50 µg, ATGP2803-100 µg, ATGP2803-250 µg, ATGP2803-500 µg, ATGP2803-1 mg, ATGP2803-10, ATGP2803-20, ATGP2803-50, ATGP2803-100, ATGP2803-250, ATGP2803-500, ATGP2803-1

Hopp K., et al (2011) . Hum. Mol. Genet. 20:2524-2534; ; Bialas N.J., et al (2009) . J. Cell Sci. 122:611-624

Can be stored at 2°C to 8°C for 1 week. For long term storage, aliquot and store at -20C to -80C. Avoid repeated freezing and thawing cycles.

Liquid in. 20 mM Tris-HCl buffer (pH 8.0) containing 10% glycerol, 0.4M urea

Other

NP_056496

Q9UPM9

Human

MGSSHHHHHH SSGLVPRGSH MGSMATASPS VFLLMVNGQV ESAQFPEYDD LYCKYCFVYG QDWAPTAGLE EGISQITSKS QDVRQALVWN FPIDVTFKST NPYGWPQIVL SVYGPDVFGN DVVRGYGAVH VPFSPGRHKR TIPMFVPEST SKLQKFTSWF MGRRPEYTDP KVVAQGEGRE VTRVRSQGFV TLLFNVVTKD MRKLGYDTGP SDTQGVLGPS PPQSFPQ