ARG65084

anti-SLC4A11 / BTR1 antibody

anti-SLC4A11 / BTR1 antibody for IHC-Formalin-fixed paraffin-embedded sections,Western blot and Human

Metabolism antibody; Neuroscience antibody; Signaling Transduction antibody

Overview

Product Description Goat Polyclonal antibody recognizes SLC4A11 / BTR1
Tested Reactivity Hu
Predict Reactivity Ms, Rat, Cow, Dog
Tested Application IHC-P, WB
Host Goat
Clonality Polyclonal
Isotype IgG
Target Name SLC4A11 / BTR1
Antigen Species Human
Immunogen C-HTSRKYLKLKNFKEE
Conjugation Un-conjugated
Alternate Names Sodium borate cotransporter 1; NaBC1; Sodium bicarbonate transporter-like protein 11; NABC1; Solute carrier family 4 member 11; CHED2; CDPD1; BTR1; dJ794I6.2; Bicarbonate transporter-related protein 1

Application Instructions

Application Suggestion
Tested Application Dilution
IHC-P3 - 5 µg/ml
WB0.3 - 1 µg/ml
Application Note WB: Recommend incubate at RT for 1h.
IHC-P: Antigen Retrieval: Steam tissue section in Citrate buffer (pH 6.0).
* The dilutions indicate recommended starting dilutions and the optimal dilutions or concentrations should be determined by the scientist.

Properties

Form Liquid
Purification Purified from goat serum by antigen affinity chromatography.
Buffer Tris saline (pH 7.3), 0.02% Sodium azide and 0.5% BSA.
Preservative 0.02% Sodium azide
Stabilizer 0.5% BSA
Concentration 0.5 mg/ml
Storage Instruction For continuous use, store undiluted antibody at 2-8°C for up to a week. For long-term storage, aliquot and store at -20°C or below. Storage in frost free freezers is not recommended. Avoid repeated freeze/thaw cycles. Suggest spin the vial prior to opening. The antibody solution should be gently mixed before use.
Note For laboratory research only, not for drug, diagnostic or other use.

Bioinformation

Database Links

GeneID: 83959 Human SLC4A11

Swiss-port # Q8NBS3 Human Sodium bicarbonate transporter-like protein 11

Background This gene encodes a voltage-regulated, electrogenic sodium-coupled borate cotransporter that is essential for borate homeostasis, cell growth and cell proliferation. Mutations in this gene have been associated with a number of endothelial corneal dystrophies including recessive corneal endothelial dystrophy 2, corneal dystrophy and perceptive deafness, and Fuchs endothelial corneal dystrophy. Multiple transcript variants encoding different isoforms have been described. [provided by RefSeq, Mar 2010]
Research Area Metabolism antibody; Neuroscience antibody; Signaling Transduction antibody
Calculated MW 100 kDa
PTM Glycosylated.