Recombinant Human NCAPG2 Protein

Cat. No.: CLPP-00150894

Product Size: 2 µg Custom size

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Product Overview

Description

CLPP-00150894 is recombinant human NCAPG2 protein

Applications

ELISA, Western Blot

Protein Length

Full length protein

Animal Free

Nature

Recombinant Protein

Species

Human

Form

Liquid

Sequence

MLLECFININYIKKEEGRRFLSCLFNWNINFIKMIHGTIKNQLQGLQKSLMVYIAEIYFRAWKKASGKILEAIENDCIQDFMFHGIHLPRRSPVHSKVREVLSYFHHQKKVRQGVEEMLYRLYKPILWRGLKARNSEVRSNAALLFVEAFPIRDPNLHAIEMDSEIQKQFEELYSLLEDPYPMVRSTGILGVCKITSKYWEMMPPTILIDLLKKVTGELAFDTSSADVRCSVFKCLPMILDNKLSHPLLEQLLPALRYSLHDNSEKVRVAFVDMLLKIKAVRAAKFWKICPMEHILVRLETDSRPVSRRLVSLIFNSFLPVNQPEEVWCERCVTLVQMNHAAARRFYQYAHEHTACTNIAKLIHVIRHCLNACIQRAVREPPEDEEEEDGREKENVTVLDKTLSVNDVACMAGLLEIIVILWKSIDRSMENNKEAKLYTINKFASVLPEYLKVFKDDRCKIPLFMLMSFMPASAVPPFSCGVISTLRSREEGAVDKSYCTLLDCLCSWGQVGHILELVDNWLPTEHAQAKSNTASKGRVQIHDTRPVKPELALVYIEYLLTHPKNRECLLSAPRKKLNHLLKALETSKADLESLLQTPGGKPRGFSEAAAPRAFGLHCRLSIHLQHKFCSEGKVYLSMLEDTGFWLESKILSFIQDQEEDYLKLHRVIYQQIIQTYLTVCKDVVMVGLGDHQFQMQLLQRSLGIMQTVKGFFYVSLLLDILKEITGSSLIQKTDSDEEVAMLLDTVQKVFQKMLECIARSFRKQPEEGLRLLYSVQRPLHEFITAVQSRHTDTPVHRGVLSTLIAGPVVEISHQLRKVSDVEELTPPEHLSDLPPFSRCLIGIIIKSSNVVRSFLDELKACVASNDIEGIVCLTAAVHIILVINAGKHKSSKVREVAATVHRKLKTFMEITLEEDSIERFLYESSSRTLGELLNS

Tags

GST tag N-Terminus

Target Information

Protein Name

NCAPG2

UniProt No.

Q86XI2

Alternative Names

CAP G2; Chromosome associated protein G2; Condensin 2 complex subunit G2; FLJ20311; hCAP G2; Leucine zipper protein 5; LUZP5; More than blood homolog; MTB; NCAPG 2; Non SMC condensin II complex subunit G2; Non SMC condensin II complex, subunit G2

Protein Function

Regulatory subunit of the condensin-2 complex, a complex which establishes mitotic chromosome architecture and is involved in physical rigidity of the chromatid axis.

Involvement in Disease

Khan-Khan-Katsanis syndrome (3KS): An autosomal recessive neurodevelopmental disorder characterized by multiple congenital anomalies affecting the ocular, renal, skeletal, and sometimes cardiac systems, defects in urogenital and limb morphogenesis, poor overall growth, microcephaly, and global developmental delay. The disease is caused by variants affecting the gene represented in this entry.

Shipping & Handling

pH: 8.0

Constituents

0.31% Glutathione, 0.79% Tris HCl.

Shipping

Shipped on dry ice.

Storage

Store at -80 °C.

For Research Use Only. Not For Clinical Use.