XK Antibody (PACO20933)
- SKU:
- PACO20933
- Product type:
- Antibody
- Reactivity:
- Human
- Host Species:
- Rabbit
- Isotype:
- IgG
- Application:
- ELISA
- Application:
- WB
- Antibody type:
- Polyclonal
- Conjugation:
- Unconjugated
Frequently bought together:
Description
抗体名: | XK Antibody (PACO20933) |
抗体コード: | PACO20933 |
サイズ: | 50ul |
宿主種: | Rabbit |
申し込み: | ELISA, WB |
推奨される希釈: | ELISA:1:1000-1:2000, WB:1:200-1:1000 |
反応性: | Human |
免疫原: | Synthetic peptide of human XK |
憲法: | Liquid |
ストレージバッファ: | -20°C, pH7.4 PBS, 0.05% NaN3, 40% Glycerol |
精製方法: | Antigen affinity purification |
抗体のクローン性: | Polyclonal |
アイソタイプ: | IgG |
Conjugate: | Non-conjugated |
![]() | Gel: 8%SDS-PAGE, Lysate: 40 µg, Lane 1-2: Human placenta and normal liver tissue, Primary antibody: PACO20933(XK Antibody) at dilution 1/400 dilution, Secondary antibody: Goat anti rabbit IgG at 1/8000 dilution, Exposure time: 1 minute. |
バックグラウンド: | This locus controls the synthesis of the Kell blood group 'precursor substance' (Kx). Mutations in this gene have been associated with McLeod syndrome, an X-linked, recessive disorder characterized by abnormalities in the neuromuscular and hematopoietic systems. The encoded protein has structural characteristics of prokaryotic and eukaryotic membrane transport proteins. |
シノニム: | X-linked Kx blood group |
UniProt Protein Function: | XK: May be involved in sodium-dependent transport of neutral amino acids or oligopeptides. Defects in XK are the cause of McLeod syndrome (MLS). It is an X-linked multisystem disorder characterized by late onset abnormalities in the neuromuscular and hematopoietic systems. Belongs to the XK family. |
UniProt Protein Details: | Protein type:Membrane protein, multi-pass; Cell surface; Membrane protein, integral Chromosomal Location of Human Ortholog: Xp21.1 Cellular Component: integral to membrane; plasma membrane Molecular Function:protein binding; transporter activity Biological Process: transport Disease: Mcleod Syndrome |
NCBI Summary: | This locus controls the synthesis of the Kell blood group 'precursor substance' (Kx). Mutations in this gene have been associated with McLeod syndrome, an X-linked, recessive disorder characterized by abnormalities in the neuromuscular and hematopoietic systems. The encoded protein has structural characteristics of prokaryotic and eukaryotic membrane transport proteins. [provided by RefSeq, Jul 2008] |
UniProt Code: | P51811 |
NCBI GenInfo Identifier: | 85700269 |
NCBI Gene ID: | 7504 |
NCBI Accession: | P51811.5 |
UniProt Secondary Accession: | P51811,Q4TTN6, Q8IUK6, Q9UC77, |
UniProt Related Accession: | P51811 |
Molecular Weight: | 50,902 Da |
NCBI Full Name: | Membrane transport protein XK |
NCBI Synonym Full Names: | X-linked Kx blood group |
NCBI Official Symbol: | XK |
NCBI Official Synonym Symbols: | KX; NA; NAC; X1k; XKR1 |
NCBI Protein Information: | membrane transport protein XK |
UniProt Protein Name: | Membrane transport protein XK |
UniProt Synonym Protein Names: | Kell complex 37 kDa component; Kx antigen; XK-related protein 1 |
Protein Family: | XK-related protein |
UniProt Gene Name: | XK |
UniProt Entry Name: | XK_HUMAN |
Antibodies |
Anti-XK Antibody (CAB15109) |
Secondary Antibody |
Anti-HRP Goat Anti-Rabbit IgG (H+L) Antibody (CABS014) |
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Anti-FITC Goat Anti-Rabbit IgG (H+L) Antibody (CABS011) |
Anti-HRP-conjugated Beta Actin Antibody (CABC028) |