Welcome to GenPrice! Check out our latest updates.

Shopping Cart (0)

Your cart is empty

Add some products to get started!

ORCTL2 Rabbit Polyclonal Antibody

Product Specifications

Background

This gene is one of several tumor-suppressing subtransferable fragments located in the imprinted gene domain of 11p15.5, an important tumor-suppressor gene region. Alterations in this region have been associated with the Beckwith-Wiedemann syndrome, Wilms tumor, rhabdomyosarcoma, adrenocortical carcinoma, and lung, ovarian, and breast cancer. This gene is imprinted, with preferential expression from the maternal allele. Mutations in this gene have been found in Wilms' tumor and lung cancer. This protein may act as a transporter of organic cations, and have a role in the transport of chloroquine and quinidine-related compounds in kidney. Several alternatively spliced transcript variants encoding different isoforms have been described. [provided by RefSeq, Oct 2015], caution:It is uncertain whether Met-1 or Met-17 is the initiator., disease:Defects in SLC22A18 are associated with breast cancer [MIM:114480]., disease:Defects in SLC22A18 are associated with lung cancer [MIM:211980]., disease:Defects in SLC22A18 are the cause of rhabdomyosarcoma type 1 (RMS1) [MIM:268210]. Rhabdomyosarcoma is a malignant tumor (sarcoma) derived from striated muscle., function:May act as a transporter of organic cations based on a proton efflux antiport mechanism. May play a role in the transport of chloroquine and quinidine-related compounds in kidney., similarity:Belongs to the major facilitator superfamily. Organic cation transporter family., subcellular location:Localized at the apical membrane surface of renal proximal tubules., subunit:Interacts with RNF167., tissue specificity:Expressed at high levels in adult and fetal kidney and liver, and adult colon. Expressed in fetal renal proximal tubules (at protein level) . Expressed at lower levels in heart, brain and lung.

Product Name Alternative

SLC22A18; BWR1A; BWSCR1A; HET; IMPT1; ITM; ORCTL2; SLC22A1L; TSSC5; Solute carrier family 22 member 18; Beckwith-Wiedemann syndrome chromosomal region 1 candidate gene A protein; Efflux transporter-like protein; Imprinted multi-membrane-spa

Gene Name

SLC22A18

Gene ID

5002

Swiss Prot

Q96BI1

Host

Rabbit

Reactivity

Human, Rat, Mouse

Clonality

Polyclonal

Conjugation

Unconjugated

Applications

WB, ICC/IF, ELISA

Purification

Affinity purification

Dilution

WB 1:500-1:2000, ICC/IF 1:200-1:1000, ELISA 1:5000-1:20000

Form

Liquid

Buffer

Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% New type preservative N.

Modification

Unmodified

Molecular Weight

43kDa

Storage Conditions

Store at 4°C short term. Aliquot and store at -20°C for 12 months. Avoid freeze/thaw cycles.

Isotype

IgG

Available Sizes

Curated Selection

Explore Other Products

Discover premium biology products from our extensive collection of 20M+ items

Human CCR5 Antibody , PE
E55A10575 50 Tests

Human CCR5 Antibody , PE

Ask
View Details
pLV2-CMV-3×FLAG-PRKAA1-IRES-Puro Plasmid
PVT59355 2 µg

pLV2-CMV-3×FLAG-PRKAA1-IRES-Puro Plasmid

Ask
View Details
Corticotropin Releasing Factor (Biotin)
546242 200 µL

Corticotropin Releasing Factor (Biotin)

Ask
View Details
Dengue NS1 protein (Serotype 3)
80-1539 100 ug

Dengue NS1 protein (Serotype 3)

Ask
View Details