ARG42095

anti-SLC6A8 antibody

anti-SLC6A8 antibody for IHC-Formalin-fixed paraffin-embedded sections,Western blot and Human,Mouse

Overview

Product Description Goat Polyclonal antibody recognizes SLC6A8
Tested Reactivity Hu, Ms
Predict Reactivity Cow, Rat, Dog, Pig
Tested Application IHC-P, WB
Host Goat
Clonality Polyclonal
Isotype IgG
Target Name SLC6A8
Antigen Species Human
Immunogen Synthetic peptide around the internal region of Human SLC6A8. (ASLANLTCDQLADRR) (NP_005620.1; NP_001136277.1; NP_001136278.1)
Conjugation Un-conjugated
Alternate Names Solute carrier family 6 member 8; CCDS1; CT1; CRT; Creatine transporter 1; CRTR; CTR5; Sodium- and chloride-dependent creatine transporter 1

Application Instructions

Application Suggestion
Tested Application Dilution
IHC-P5 µg/ml
WB0.1 - 0.3 µg/ml
Application Note IHC-P: Antigen Retrieval: Steam tissue section in Citrate buffer (pH 6.0).
WB: Recommend incubate at RT for 1h.
* The dilutions indicate recommended starting dilutions and the optimal dilutions or concentrations should be determined by the scientist.
Observed Size ~ 70 kDa

Properties

Form Liquid
Purification Affinity purified
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: 102857 Mouse SLC6A8

GeneID: 6535 Human SLC6A8

Swiss-port # P48029 Human Sodium- and chloride-dependent creatine transporter 1

Swiss-port # Q8VBW1 Mouse Sodium- and chloride-dependent creatine transporter 1

Gene Symbol SLC6A8
Gene Full Name solute carrier family 6 (neurotransmitter transporter), member 8
Background The protein encoded by this gene is a plasma membrane protein whose function is to transport creatine into and out of cells. Defects in this gene can result in X-linked creatine deficiency syndrome. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2008]
Function Required for the uptake of creatine in muscles and brain. [UniProt]
Cellular Localization Membrane; Multi-pass membrane protein. [UniProt]
Calculated MW 71 kDa